1. Anti-infection
  2. HBV Reverse Transcriptase
  3. Adefovir

アデフォビル  (Synonyms: Adefovir)

製品番号: HY-B1826 純度: 99.55%
COA 取扱説明書 Technical Support

Adefovir (GS-0393) is an adenosine monophosphate analog antiviral agent that after intracellular conversion to Adefovir diphosphate inhibits HBV DNA polymerase. Adefovir has an IC50 of 0.7 μM against HBV in the HepG2.2.15 cell line. Adefovir has good antiviral activity against several viruses, including HBV and herpesviruses.

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Adefovir

アデフォビル 構造式

CAS 番号 : 106941-25-7

容量 価格(税別) 在庫状況 数量
25 mg $50 在庫あり
50 mg $80 在庫あり
100 mg $120 在庫あり
200 mg   お問い合わせ  
500 mg   お問い合わせ  

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カスタマーレビュー

Based on 2 publication(s) in Google Scholar

Other Forms of Adefovir:

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製品説明

Adefovir (GS-0393) is an adenosine monophosphate analog antiviral agent that after intracellular conversion to Adefovir diphosphate inhibits HBV DNA polymerase. Adefovir has an IC50 of 0.7 μM against HBV in the HepG2.2.15 cell line. Adefovir has good antiviral activity against several viruses, including HBV and herpesviruses[1][2][3].

IC50 & Target

HBV[1][2][3];
DNA polymerase[1][2]

Cellular Effect
Cell Line Type Value Description References
C-33-A IC50
7.8 3
Compound: 1, PMEA
Antiproliferative activity against human C33A cells after 72 hrs by flow cytometric analysis
Antiproliferative activity against human C33A cells after 72 hrs by flow cytometric analysis
[PMID: 24686012]
C3H/3T3 EC50
0.53 3
Compound: PMEA, Adefovir
Inhibition of murine sarcoma virus-induced transformation of mouse embryo fibroblast C3H/3T3 cells after 6 days
Inhibition of murine sarcoma virus-induced transformation of mouse embryo fibroblast C3H/3T3 cells after 6 days
[PMID: 18556209]
C3H/3T3 EC50
2.1 3
Compound: PMEA
Antiviral against Moloney murine sarcoma virus infected in mouse C3H/3T3 cells assessed as inhibition of virus-induced cell transformation after 6 days post infection by microscopic analysis
Antiviral against Moloney murine sarcoma virus infected in mouse C3H/3T3 cells assessed as inhibition of virus-induced cell transformation after 6 days post infection by microscopic analysis
[PMID: 21429755]
BSC-1 CC50
210.1 3
Compound: PMEA
Cytotoxicity against african green monkey BSC1 cells
Cytotoxicity against african green monkey BSC1 cells
[PMID: 17420214]
C8166 EC50
1.7 3
Compound: PMEA
Concentration required to inhibit p24 viral antigen production by 50% in C-8166 cells
Concentration required to inhibit p24 viral antigen production by 50% in C-8166 cells
10.1016/0960-894X(95)00208-B
BSC-1 EC50
125.9 3
Compound: PMEA
Antiviral activity against Simian virus 40 PML2 DAR in african green monkey BSC1 cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against Simian virus 40 PML2 DAR in african green monkey BSC1 cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 17420214]
C8166 EC50
7 3
Compound: PMEA, Adefovir
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus type 2 ROD infected in C8166 cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus type 2 ROD infected in C8166 cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
[PMID: 21803462]
C-33-A IC50
7.8 3
Compound: 1, PMEA
Antiproliferative activity against human C33A cells after 72 hrs by flow cytometric analysis
Antiproliferative activity against human C33A cells after 72 hrs by flow cytometric analysis
[PMID: 24686012]
BSC-1 EC50
157.7 3
Compound: PMEA
Antiviral activity against Simian virus 40 A2895 in african green monkey BSC1 cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against Simian virus 40 A2895 in african green monkey BSC1 cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 17420214]
CCRF-CEM CC50
≥ 250 3
Compound: PMEA
Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation after 72 hrs by coulter counter analysis
Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation after 72 hrs by coulter counter analysis
[PMID: 21429755]
C3H/3T3 EC50
2.1 3
Compound: PMEA
Antiviral against Moloney murine sarcoma virus infected in mouse C3H/3T3 cells assessed as inhibition of virus-induced cell transformation after 6 days post infection by microscopic analysis
Antiviral against Moloney murine sarcoma virus infected in mouse C3H/3T3 cells assessed as inhibition of virus-induced cell transformation after 6 days post infection by microscopic analysis
[PMID: 21429755]
BSC-1 EC50
168 3
Compound: PMEA
Antiviral activity against Simian virus 40 PML1 EK in african green monkey BSC1 cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against Simian virus 40 PML1 EK in african green monkey BSC1 cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 17420214]
CCRF-CEM EC50
10.4 3
Compound: 1, PMEA, Adefovir
Antiviral activity against HIV 1 3B infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
Antiviral activity against HIV 1 3B infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
[PMID: 21565516]
C-33-A IC50
7.8 3
Compound: 1, PMEA
Antiproliferative activity against human C33A cells after 72 hrs by flow cytometric analysis
Antiproliferative activity against human C33A cells after 72 hrs by flow cytometric analysis
[PMID: 24686012]
C3H/3T3 EC50
0.25 6
Compound: PMEA (adefovir)
Inhibition of moloney sarcoma virus (MSV) induced cytopathicity in C3H/3T3 embryo fibroblast cells
Inhibition of moloney sarcoma virus (MSV) induced cytopathicity in C3H/3T3 embryo fibroblast cells
[PMID: 11960502]
C3H/3T3 EC50
0.53 3
Compound: PMEA, Adefovir
Inhibition of murine sarcoma virus-induced transformation of mouse embryo fibroblast C3H/3T3 cells after 6 days
Inhibition of murine sarcoma virus-induced transformation of mouse embryo fibroblast C3H/3T3 cells after 6 days
[PMID: 18556209]
CCRF-CEM CC50
164 3
Compound: 1, PMEA, Adefovir
Cytotoxicity against human CEM cells assessed as growth inhibition after 3 days by coulter counting analysis
Cytotoxicity against human CEM cells assessed as growth inhibition after 3 days by coulter counting analysis
[PMID: 21565516]
C3H/3T3 EC50
0.25 6
Compound: PMEA (adefovir)
Inhibition of moloney sarcoma virus (MSV) induced cytopathicity in C3H/3T3 embryo fibroblast cells
Inhibition of moloney sarcoma virus (MSV) induced cytopathicity in C3H/3T3 embryo fibroblast cells
[PMID: 11960502]
CCRF-CEM EC50
18 3
Compound: PMEA
In vitro anti -HIV activity tested against CEM cells infected with HIV by XTT assay
In vitro anti -HIV activity tested against CEM cells infected with HIV by XTT assay
[PMID: 1323678]
C8166 EC50
7 3
Compound: PMEA, Adefovir
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus type 2 ROD infected in C8166 cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus type 2 ROD infected in C8166 cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
[PMID: 21803462]
C3H/3T3 EC50
0.53 3
Compound: PMEA, Adefovir
Inhibition of murine sarcoma virus-induced transformation of mouse embryo fibroblast C3H/3T3 cells after 6 days
Inhibition of murine sarcoma virus-induced transformation of mouse embryo fibroblast C3H/3T3 cells after 6 days
[PMID: 18556209]
CCRF-CEM IC50
24 3
Compound: 1, PMEA
Cytostatic activity against human CEM cells after 72 hrs by coulter counting analysis
Cytostatic activity against human CEM cells after 72 hrs by coulter counting analysis
[PMID: 24686012]
C3H/3T3 EC50
2.1 3
Compound: PMEA
Antiviral against Moloney murine sarcoma virus infected in mouse C3H/3T3 cells assessed as inhibition of virus-induced cell transformation after 6 days post infection by microscopic analysis
Antiviral against Moloney murine sarcoma virus infected in mouse C3H/3T3 cells assessed as inhibition of virus-induced cell transformation after 6 days post infection by microscopic analysis
[PMID: 21429755]
C8166 EC50
1.5 3
Compound: PMEA
Compound was evaluated for the inhibition of p24 viral antigen production in C-8166 cells.
Compound was evaluated for the inhibition of p24 viral antigen production in C-8166 cells.
10.1016/0960-894X(95)00585-H
C8166 EC50
1.7 3
Compound: PMEA
Concentration required to inhibit p24 viral antigen production by 50% in C-8166 cells
Concentration required to inhibit p24 viral antigen production by 50% in C-8166 cells
10.1016/0960-894X(95)00208-B
CCRF-CEM EC50
5.5 3
Compound: PMEA, Adefovir
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus 1 3B infected in CEM cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus 1 3B infected in CEM cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
[PMID: 21803462]
C8166 EC50
1.5 3
Compound: PMEA
Compound was evaluated for the inhibition of p24 viral antigen production in C-8166 cells.
Compound was evaluated for the inhibition of p24 viral antigen production in C-8166 cells.
10.1016/0960-894X(95)00585-H
CCRF-CEM EC50
7 3
Compound: PMEA, adefovir
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopy
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopy
[PMID: 21745746]
C8166 EC50
1.7 3
Compound: PMEA
Concentration required to inhibit p24 viral antigen production by 50% in C-8166 cells
Concentration required to inhibit p24 viral antigen production by 50% in C-8166 cells
10.1016/0960-894X(95)00208-B
CCRF-CEM CC50
0.056 92
Compound: PMEA
Cytotoxicity against CEM (human lymphoblastic leukemia) cells in vitro.
Cytotoxicity against CEM (human lymphoblastic leukemia) cells in vitro.
[PMID: 14584956]
CCRF-CEM CC50
50 3
Compound: 1, PMEA
Cytotoxicity against CEM/O cells
Cytotoxicity against CEM/O cells
[PMID: 16335932]
CCRF-CEM EC50
7 3
Compound: PMEA
Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
[PMID: 21429755]
C8166 EC50
7 3
Compound: PMEA, Adefovir
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus type 2 ROD infected in C8166 cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus type 2 ROD infected in C8166 cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
[PMID: 21803462]
CCRF-CEM EC50
7.4 3
Compound: PMEA, adefovir
Antiviral activity against Human immunodeficiency virus type1 3B infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus type1 3B infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopic analysis
[PMID: 21745746]
CCRF-CEM CC50
85 3
Compound: PMEA, Adefovir
Cytotoxicity against human CEM cells
Cytotoxicity against human CEM cells
[PMID: 21803462]
CCRF-CEM CC50
0.056 2
Compound: PMEA
Cytotoxicity against CEM (human lymphoblastic leukemia) cells in vitro.
Cytotoxicity against CEM (human lymphoblastic leukemia) cells in vitro.
[PMID: 14584956]
CCRF-CEM EC50
7.4 3
Compound: PMEA
Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
[PMID: 21429755]
CCRF-CEM CC50
164 3
Compound: 1, PMEA, Adefovir
Cytotoxicity against human CEM cells assessed as growth inhibition after 3 days by coulter counting analysis
Cytotoxicity against human CEM cells assessed as growth inhibition after 3 days by coulter counting analysis
[PMID: 21565516]
CCRF-CEM CC50
>= 50 3
Compound: 1, PMEA
Cytotoxicity against human CEM cells
Cytotoxicity against human CEM cells
[PMID: 24686012]
CCRF-CEM EC50
8.2 3
Compound: 1, PMEA
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
[PMID: 24686012]
CCRF-CEM CC50
50 3
Compound: 1, PMEA
Cytotoxicity against CEM/O cells
Cytotoxicity against CEM/O cells
[PMID: 16335932]
CCRF-CEM CC50
164 3
Compound: 1, PMEA, Adefovir
Cytotoxicity against human CEM cells assessed as growth inhibition after 3 days by coulter counting analysis
Cytotoxicity against human CEM cells assessed as growth inhibition after 3 days by coulter counting analysis
[PMID: 21565516]
CCRF-CEM EC50
8.4 3
Compound: 1, PMEA
Antiviral activity against Human immunodeficiency virus 1 3B infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus 1 3B infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
[PMID: 24686012]
CCRF-CEM CC50
69 3
Compound: 2
In vitro cytotoxic concentration against CEM cells
In vitro cytotoxic concentration against CEM cells
[PMID: 11327587]
CCRF-CEM CC50
>= 250 3
Compound: PMEA
Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation after 72 hrs by coulter counter analysis
Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation after 72 hrs by coulter counter analysis
[PMID: 21429755]
CCRF-CEM EC50
8.6 3
Compound: 1, PMEA, Adefovir
Antiviral activity against HIV 2 ROD infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
Antiviral activity against HIV 2 ROD infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
[PMID: 21565516]
CCRF-CEM CC50
85 3
Compound: PMEA, Adefovir
Cytotoxicity against human CEM cells
Cytotoxicity against human CEM cells
[PMID: 21803462]
CCRF-CEM CC50
69 3
Compound: 2
In vitro cytotoxic concentration against CEM cells
In vitro cytotoxic concentration against CEM cells
[PMID: 11327587]
CHO CC50
≥ 2000 3
Compound: Adefovir
Cytotoxicity against CHO cells after 120 hrs by Cell-Titer Glo assay
Cytotoxicity against CHO cells after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
CCRF-CEM EC50
5.5 3
Compound: PMEA, Adefovir
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus 1 3B infected in CEM cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus 1 3B infected in CEM cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
[PMID: 21803462]
CCRF-CEM CC50
>= 250 3
Compound: PMEA
Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation after 72 hrs by coulter counter analysis
Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation after 72 hrs by coulter counter analysis
[PMID: 21429755]
CHO CC50
1.4 3
Compound: Adefovir
Ratio of CC50 for CHO cells to CC50 for CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
Ratio of CC50 for CHO cells to CC50 for CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
CCRF-CEM EC50
10.4 3
Compound: 1, PMEA, Adefovir
Antiviral activity against HIV 1 3B infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
Antiviral activity against HIV 1 3B infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
[PMID: 21565516]
CCRF-CEM CC50
>= 50 3
Compound: 1, PMEA
Cytotoxicity against human CEM cells
Cytotoxicity against human CEM cells
[PMID: 24686012]
CHO CC50
3 3
Compound: Adefovir
Cytotoxicity against CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
Cytotoxicity against CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
CCRF-CEM EC50
8.6 3
Compound: 1, PMEA, Adefovir
Antiviral activity against HIV 2 ROD infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
Antiviral activity against HIV 2 ROD infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
[PMID: 21565516]
CCRF-CEM EC50
0.0033 2
Compound: PMEA
Antiviral activity against HIV-1 (IIIB) in CEM (human leukemia) cells.
Antiviral activity against HIV-1 (IIIB) in CEM (human leukemia) cells.
[PMID: 14584956]
H9 CC50
> 30 3
Compound: PMEA, Adefovir
Cytotoxicity against PAP-activated human H9 cells on day 7 by MTT assay
Cytotoxicity against PAP-activated human H9 cells on day 7 by MTT assay
[PMID: 21803462]
CCRF-CEM EC50
0.0066 2
Compound: PMEA
Antiviral activity against HIV-2 (ROD) in CEM (human leukemia) cells.
Antiviral activity against HIV-2 (ROD) in CEM (human leukemia) cells.
[PMID: 14584956]
CCRF-CEM EC50
0.0033 92
Compound: PMEA
Antiviral activity against HIV-1 (IIIB) in CEM (human leukemia) cells.
Antiviral activity against HIV-1 (IIIB) in CEM (human leukemia) cells.
[PMID: 14584956]
H9 EC50
1.1 3
Compound: PMEA, Adefovir
Antiviral activity against 125 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
Antiviral activity against 125 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
[PMID: 21803462]
CCRF-CEM EC50
1.8 6
Compound: PMEA (adefovir)
Inhibition of Human immunodeficiency virus (HIV) -1 III B strain induced cytopathicity in CEM cell line
Inhibition of Human immunodeficiency virus (HIV) -1 III B strain induced cytopathicity in CEM cell line
[PMID: 11960502]
CCRF-CEM EC50
7.4 3
Compound: PMEA
Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
[PMID: 21429755]
CCRF-CEM EC50
0.0066 92
Compound: PMEA
Antiviral activity against HIV-2 (ROD) in CEM (human leukemia) cells.
Antiviral activity against HIV-2 (ROD) in CEM (human leukemia) cells.
[PMID: 14584956]
H9 EC50
7.9 3
Compound: PMEA, Adefovir
Antiviral activity against 6250 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
Antiviral activity against 6250 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
[PMID: 21803462]
CCRF-CEM EC50
10 3
Compound: 2
In vitro antiviral activity against HIV-2 in CEM cells
In vitro antiviral activity against HIV-2 in CEM cells
[PMID: 11327587]
HEK-293T CC50
> 100 3
Compound: PMEA
Cytotoxicity against human 293T cells assessed as inhibition of cell proliferation by tetrazolium dye method
Cytotoxicity against human 293T cells assessed as inhibition of cell proliferation by tetrazolium dye method
[PMID: 17470654]
CCRF-CEM EC50
7 3
Compound: PMEA
Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
[PMID: 21429755]
CCRF-CEM EC50
10.4 3
Compound: 1, PMEA, Adefovir
Antiviral activity against HIV 1 3B infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
Antiviral activity against HIV 1 3B infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
[PMID: 21565516]
CCRF-CEM EC50
8.4 3
Compound: 1, PMEA
Antiviral activity against Human immunodeficiency virus 1 3B infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus 1 3B infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
[PMID: 24686012]
HEL 299 EC50
> 183 3
Compound: 3a, PMEA
Antiviral activity against Camelpox virus CML1 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
Antiviral activity against Camelpox virus CML1 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
[PMID: 17893157]
CCRF-CEM EC50
18 3
Compound: PMEA
In vitro anti -HIV activity tested against CEM cells infected with HIV by XTT assay
In vitro anti -HIV activity tested against CEM cells infected with HIV by XTT assay
[PMID: 1323678]
HEL 299 EC50
> 183 3
Compound: 3a, PMEA
Antiviral activity against Camelpox virus CML14 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
Antiviral activity against Camelpox virus CML14 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
[PMID: 17893157]
CCRF-CEM EC50
2.5 6
Compound: PMEA (adefovir)
Inhibition of Human immunodeficiency virus (HIV)-2 ROD strain induced cytopathicity in CEM cell line
Inhibition of Human immunodeficiency virus (HIV)-2 ROD strain induced cytopathicity in CEM cell line
[PMID: 11960502]
CCRF-CEM EC50
7 3
Compound: PMEA, adefovir
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopy
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopy
[PMID: 21745746]
CCRF-CEM EC50
8.2 3
Compound: 1, PMEA
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
[PMID: 24686012]
HEL 299 CC50
211 3
Compound: 3a, PMEA
Cytotoxicity against HEL299 cells after 4 days by Z1 Coulter counting analysis
Cytotoxicity against HEL299 cells after 4 days by Z1 Coulter counting analysis
[PMID: 17893157]
CCRF-CEM EC50
5.5 3
Compound: PMEA, Adefovir
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus 1 3B infected in CEM cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
Antiviral activity against 100 TCID50 wild-type Human immunodeficiency virus 1 3B infected in CEM cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
[PMID: 21803462]
HeLa CC50
> 250 3
Compound: 1, PMEA, Adefovir
Cytotoxicity against human HeLa cells assessed as growth inhibition after 3 days by coulter counting analysis
Cytotoxicity against human HeLa cells assessed as growth inhibition after 3 days by coulter counting analysis
[PMID: 21565516]
CCRF-CEM EC50
7.4 3
Compound: PMEA, adefovir
Antiviral activity against Human immunodeficiency virus type1 3B infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus type1 3B infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopic analysis
[PMID: 21745746]
CCRF-CEM EC50
7 3
Compound: 2
In vitro antiviral activity against HIV-1 in CEM cells
In vitro antiviral activity against HIV-1 in CEM cells
[PMID: 11327587]
HeLa IC50
181 3
Compound: 1, PMEA
Cytostatic activity against human HeLa cells after 72 hrs by coulter counting analysis
Cytostatic activity against human HeLa cells after 72 hrs by coulter counting analysis
[PMID: 24686012]
CCRF-CEM EC50
18 3
Compound: PMEA
In vitro anti -HIV activity tested against CEM cells infected with HIV by XTT assay
In vitro anti -HIV activity tested against CEM cells infected with HIV by XTT assay
[PMID: 1323678]
CCRF-CEM EC50
7 3
Compound: PMEA
Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
Antiviral activity against HIV2 ROD infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
[PMID: 21429755]
HepG2 IC50
42.1 3
Compound: PMEA, 1
Antiviral activity against Hepatitis B virus infected human HepG2 cells after 9 days by MTT assay
Antiviral activity against Hepatitis B virus infected human HepG2 cells after 9 days by MTT assay
[PMID: 17888662]
CCRF-CEM EC50
7 3
Compound: PMEA, adefovir
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopy
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopy
[PMID: 21745746]
CCRF-CEM EC50
7 3
Compound: 2
In vitro antiviral activity against HIV-1 in CEM cells
In vitro antiviral activity against HIV-1 in CEM cells
[PMID: 11327587]
HepG2 2.2.15 IC50
0.517 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBV DNA replication after 9 days by PCR
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBV DNA replication after 9 days by PCR
[PMID: 20000776]
CCRF-CEM EC50
10 3
Compound: 2
In vitro antiviral activity against HIV-2 in CEM cells
In vitro antiviral activity against HIV-2 in CEM cells
[PMID: 11327587]
CCRF-CEM EC50
7.4 3
Compound: PMEA
Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
Antiviral activity against HIV1 3B infected in human CEM cells assessed as inhibition of virus-induced syncytium formation after 4 to 5 days by microscopic analysis
[PMID: 21429755]
HepG2 2.2.15 IC50
0.517 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of viral replication after 9 days by fluorescence PCR method
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of viral replication after 9 days by fluorescence PCR method
[PMID: 23353737]
CCRF-CEM EC50
1.8 6
Compound: PMEA (adefovir)
Inhibition of Human immunodeficiency virus (HIV) -1 III B strain induced cytopathicity in CEM cell line
Inhibition of Human immunodeficiency virus (HIV) -1 III B strain induced cytopathicity in CEM cell line
[PMID: 11960502]
CCRF-CEM EC50
7.4 3
Compound: PMEA, adefovir
Antiviral activity against Human immunodeficiency virus type1 3B infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus type1 3B infected in human CEM cells assessed as HIV-induced CEM giant cell formation after 4 days by microscopic analysis
[PMID: 21745746]
HepG2 2.2.15 EC50
1.3 3
Compound: Adefovir
Antiviral activity against wild type Hepatitis B virus infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization method
Antiviral activity against wild type Hepatitis B virus infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization method
[PMID: 21930377]
CCRF-CEM EC50
8.2 3
Compound: 1, PMEA
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus type 2 ROD infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
[PMID: 24686012]
CCRF-CEM EC50
2.5 6
Compound: PMEA (adefovir)
Inhibition of Human immunodeficiency virus (HIV)-2 ROD strain induced cytopathicity in CEM cell line
Inhibition of Human immunodeficiency virus (HIV)-2 ROD strain induced cytopathicity in CEM cell line
[PMID: 11960502]
HepG2 2.2.15 EC50
1.6 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204V mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204V mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
CCRF-CEM IC50
285 6
Compound: 4
Cellular toxic effect was determined in CEM cells
Cellular toxic effect was determined in CEM cells
[PMID: 11606136]
CCRF-CEM EC50
8.4 3
Compound: 1, PMEA
Antiviral activity against Human immunodeficiency virus 1 3B infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
Antiviral activity against Human immunodeficiency virus 1 3B infected in human CEM cells assessed as inhibition of virus-induced giant cell formation after 4 to 5 days by microscopic analysis
[PMID: 24686012]
HepG2 2.2.15 EC50
1.9 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204I mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204I mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
CCRF-CEM EC50
8.6 3
Compound: 1, PMEA, Adefovir
Antiviral activity against HIV 2 ROD infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
Antiviral activity against HIV 2 ROD infected in CEM cells assessed as inhibition of virus-induced giant cell formation after 4 days by microscopy
[PMID: 21565516]
CCRF-CEM IC50
24 3
Compound: 1, PMEA
Cytostatic activity against human CEM cells after 72 hrs by coulter counting analysis
Cytostatic activity against human CEM cells after 72 hrs by coulter counting analysis
[PMID: 24686012]
HepG2 2.2.15 EC50
2.1 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M/M204V double mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hyb
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M/M204V double mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hyb
[PMID: 21930377]
CCRF-CEM IC50
2 6
Compound: 4
Inhibition of antiviral activity against moloney murine sarcoma virus(MSV)in CEM cells in cell protection assay
Inhibition of antiviral activity against moloney murine sarcoma virus(MSV)in CEM cells in cell protection assay
[PMID: 11606136]
CCRF-CEM IC50
24 3
Compound: 1, PMEA
Cytostatic activity against human CEM cells after 72 hrs by coulter counting analysis
Cytostatic activity against human CEM cells after 72 hrs by coulter counting analysis
[PMID: 24686012]
HepG2 2.2.15 CC50
200 3
Compound: Adefovir
Cytotoxicity in human HepG2.215 cells assessed as reduction in cell viability after 5 days by CCK8 assay
Cytotoxicity in human HepG2.215 cells assessed as reduction in cell viability after 5 days by CCK8 assay
[PMID: 28082068]
CCRF-CEM IC50
285 6
Compound: 4
Cellular toxic effect was determined in CEM cells
Cellular toxic effect was determined in CEM cells
[PMID: 11606136]
HepG2 2.2.15 IC50
215 3
Compound: Adefovir
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as HBeAg secretion after 9 days by ELISA
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as HBeAg secretion after 9 days by ELISA
[PMID: 25650312]
CCRF-CEM IC50
2 6
Compound: 4
Inhibition of antiviral activity against moloney murine sarcoma virus(MSV)in CEM cells in cell protection assay
Inhibition of antiviral activity against moloney murine sarcoma virus(MSV)in CEM cells in cell protection assay
[PMID: 11606136]
HepG2 2.2.15 IC50
257 3
Compound: Adefovir
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as surface antigen HBsAg secretion after 9 days by ELISA
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as surface antigen HBsAg secretion after 9 days by ELISA
[PMID: 25650312]
CHO CC50
>= 2 2
Compound: Adefovir
Cytotoxicity against CHO cells after 120 hrs by Cell-Titer Glo assay
Cytotoxicity against CHO cells after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
HepG2 2.2.15 IC50
286 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg production after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg production after 9 days by ELISA
[PMID: 23353737]
CHO CC50
3 3
Compound: Adefovir
Cytotoxicity against CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
Cytotoxicity against CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
HepG2 2.2.15 IC50
286 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg level after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg level after 9 days by ELISA
[PMID: 20000776]
CHO CC50
1.4 3
Compound: Adefovir
Ratio of CC50 for CHO cells to CC50 for CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
Ratio of CC50 for CHO cells to CC50 for CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
HepG2 2.2.15 IC50
305 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg production after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg production after 9 days by ELISA
[PMID: 23353737]
CHO IC50
28 3
Compound: Adefovir
TP_TRANSPORTER: inhibition of 6-Carboxyfluorescein uptake in OAT1-expressing CHO cells
TP_TRANSPORTER: inhibition of 6-Carboxyfluorescein uptake in OAT1-expressing CHO cells
[PMID: 10929807]
CEM-SS CC50
> 10 3
Compound: 1
Compound was tested for antiviral activity against the CEM-SS cell lines infected with HIV-1.
Compound was tested for antiviral activity against the CEM-SS cell lines infected with HIV-1.
[PMID: 8960556]
HepG2 2.2.15 IC50
305 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg level after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg level after 9 days by ELISA
[PMID: 20000776]
CEM-SS EC50
0.42 3
Compound: 1
Compound was tested for antiviral activity against the CEM-SS cell lines infected with HIV-1.
Compound was tested for antiviral activity against the CEM-SS cell lines infected with HIV-1.
[PMID: 8960556]
HepG2 2.2.15 CC50
490 3
Compound: Adefovir
Cytotoxicity against human HepG2.2.15 cells assessed as cell death after 9 days by MTS assay
Cytotoxicity against human HepG2.2.15 cells assessed as cell death after 9 days by MTS assay
[PMID: 25650312]
HepG2 2.2.15 EC50
5.5 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
H9 CC50
>30 3
Compound: PMEA, Adefovir
Cytotoxicity against PAP-activated human H9 cells on day 7 by MTT assay
Cytotoxicity against PAP-activated human H9 cells on day 7 by MTT assay
[PMID: 21803462]
CHO CC50
1.4 3
Compound: Adefovir
Ratio of CC50 for CHO cells to CC50 for CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
Ratio of CC50 for CHO cells to CC50 for CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
HepG2 2.2.15 CC50
540 3
Compound: Adefovir
Cytotoxicity against human HepG2(2.2.15) cells compound treated for 48 hrs followed by incubation for 9 days by MTT assay
Cytotoxicity against human HepG2(2.2.15) cells compound treated for 48 hrs followed by incubation for 9 days by MTT assay
[PMID: 23353737]
H9 EC50
1.1 3
Compound: PMEA, Adefovir
Antiviral activity against 125 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
Antiviral activity against 125 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
[PMID: 21803462]
CHO CC50
3 3
Compound: Adefovir
Cytotoxicity against CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
Cytotoxicity against CHO cells expressing hOAT1 after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
HepG2 2.2.15 CC50
57 3
Compound: adefovir
Cytotoxicity against HepG2.2.15 cells after 6 hrs by MTT assay
Cytotoxicity against HepG2.2.15 cells after 6 hrs by MTT assay
[PMID: 17499889]
H9 EC50
7.9 3
Compound: PMEA, Adefovir
Antiviral activity against 6250 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
Antiviral activity against 6250 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
[PMID: 21803462]
CHO CC50
>= 2000 3
Compound: Adefovir
Cytotoxicity against CHO cells after 120 hrs by Cell-Titer Glo assay
Cytotoxicity against CHO cells after 120 hrs by Cell-Titer Glo assay
[PMID: 19001108]
HepG2 2.2.15 EC50
7.8 3
Compound: Adefovir
Antiviral activity against adefovir-resistant Hepatitis B virus harboring reverse transcriptase N236T mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization meth
Antiviral activity against adefovir-resistant Hepatitis B virus harboring reverse transcriptase N236T mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization meth
[PMID: 21930377]
H9 EC50
17.76 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade A isolate 4113 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade A isolate 4113 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
CHO IC50
28 3
Compound: Adefovir
TP_TRANSPORTER: inhibition of 6-Carboxyfluorescein uptake in OAT1-expressing CHO cells
TP_TRANSPORTER: inhibition of 6-Carboxyfluorescein uptake in OAT1-expressing CHO cells
[PMID: 10929807]
Huh-7 EC50
1.3 3
Compound: adefovir
Antiviral activity against adefovir-resistant wild type HBV in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant wild type HBV in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
H9 EC50
0.32 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade A/E isolate 2165 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade A/E isolate 2165 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
Huh-7 EC50
1.5 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204V mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204V mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
H9 EC50
1.85 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade B isolate 1722 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade B isolate 1722 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
Huh-7 EC50
1.6 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase L180M mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase L180M mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
H9 EC50
1.02 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade B isolate 2056 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade B isolate 2056 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
Huh-7 EC50
1.6 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase LM/reverse transcriptase MV double mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase LM/reverse transcriptase MV double mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
H9 EC50
3.51 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade B isolate 2101 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade B isolate 2101 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
Huh-7 EC50
1.8 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204I mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204I mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
H9 EC50
1.45 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade C isolate 2914 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade C isolate 2914 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
E6SM EC50
0.024 2
Compound: PMEA
Antiviral activity against G strain of HSV-2 in E6SM cells.
Antiviral activity against G strain of HSV-2 in E6SM cells.
[PMID: 14584956]
Huh-7 EC50
6 3
Compound: PMEA, Adefovir
Antiviral activity against Hepatitis B virus infected in human HuH7 cells assessed as reduction in viral DNA level treated day 3 to day 8 post transfection by real time quantitative PCR analysis
Antiviral activity against Hepatitis B virus infected in human HuH7 cells assessed as reduction in viral DNA level treated day 3 to day 8 post transfection by real time quantitative PCR analysis
[PMID: 21803462]
H9 EC50
2.74 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade C isolate 4110 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade C isolate 4110 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
E6SM EC50
0.024 2
Compound: PMEA
Antiviral activity against KOS strain of HSV-1 in E6SM cells.
Antiviral activity against KOS strain of HSV-1 in E6SM cells.
[PMID: 14584956]
Huh-7 EC50
7.7 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase 236T mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase 236T mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
E6SM EC50
7 6
Compound: PMEA (adefovir)
Inhibition of Herpes simplex virus-1, KOS strain induced cytopathicity in E6SM cell line
Inhibition of Herpes simplex virus-1, KOS strain induced cytopathicity in E6SM cell line
[PMID: 11960502]
H9 EC50
0.19 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade F isolate 2338 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade F isolate 2338 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
L1210 IC50
3 3
Compound: 1, PMEA
Cytostatic activity against mouse L1210 cells after 48 hrs by coulter counting analysis
Cytostatic activity against mouse L1210 cells after 48 hrs by coulter counting analysis
[PMID: 24686012]
H9 EC50
0.22 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade G isolate 3187 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade G isolate 3187 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
E6SM EC50
7 6
Compound: PMEA (adefovir)
Inhibition of Herpes simplex virus-2 (G strain) induced cytopathicity in E6SM cell line
Inhibition of Herpes simplex virus-2 (G strain) induced cytopathicity in E6SM cell line
[PMID: 11960502]
MT4 EC50
22 3
Compound: PMEA
Concentration required to inhibit HIV-1-induced cytopathic effect by 50% in MT-4 cells
Concentration required to inhibit HIV-1-induced cytopathic effect by 50% in MT-4 cells
10.1016/0960-894X(95)00208-B
HEK-293T CC50
>100 3
Compound: PMEA
Cytotoxicity against human 293T cells assessed as inhibition of cell proliferation by tetrazolium dye method
Cytotoxicity against human 293T cells assessed as inhibition of cell proliferation by tetrazolium dye method
[PMID: 17470654]
E6SM EC50
7 6
Compound: PMEA (adefovir)
Inhibition of thymidine kinase deficient Herpes simplex virus-1 VMW 1837 strain induced cytopathicity in E6SM cell line
Inhibition of thymidine kinase deficient Herpes simplex virus-1 VMW 1837 strain induced cytopathicity in E6SM cell line
[PMID: 11960502]
PBMC CC50
> 30 3
Compound: PMEA, Adefovir
Cytotoxicity against PAP-activated human PBMC on day 7 by MTT assay
Cytotoxicity against PAP-activated human PBMC on day 7 by MTT assay
[PMID: 21803462]
H9 CC50
> 30 3
Compound: PMEA, Adefovir
Cytotoxicity against PAP-activated human H9 cells on day 7 by MTT assay
Cytotoxicity against PAP-activated human H9 cells on day 7 by MTT assay
[PMID: 21803462]
Vero IC50
119 3
Compound: 1
Concentration that reduced plaque formation by 50% was measured in HSV-2 infected vero cells in vitro
Concentration that reduced plaque formation by 50% was measured in HSV-2 infected vero cells in vitro
[PMID: 8021925]
H9 EC50
0.19 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade F isolate 2338 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade F isolate 2338 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
0.22 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade G isolate 3187 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade G isolate 3187 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
WI-38 CC50
124.7 3
Compound: PMEA
Cytotoxicity against human WI38 cells by neutral red assay
Cytotoxicity against human WI38 cells by neutral red assay
[PMID: 18285481]
WI-38 EC50
95.8 3
Compound: PMEA
Antimicrobial activity against BK polyomavirus ATCC VR837 infected in human WI38 cells assessed as reduction in viral titer after 7 days by PCR analysis
Antimicrobial activity against BK polyomavirus ATCC VR837 infected in human WI38 cells assessed as reduction in viral titer after 7 days by PCR analysis
[PMID: 18285481]
H9 EC50
0.32 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade A/E isolate 2165 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade A/E isolate 2165 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
0.32 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade D isolate 1649 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade D isolate 1649 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
1.02 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade B isolate 2056 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade B isolate 2056 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
1.1 3
Compound: PMEA, Adefovir
Antiviral activity against 125 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
Antiviral activity against 125 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
[PMID: 21803462]
H9 EC50
1.45 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade C isolate 2914 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade C isolate 2914 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
1.85 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade B isolate 1722 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade B isolate 1722 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
17.76 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade A isolate 4113 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade A isolate 4113 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
2.74 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade C isolate 4110 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade C isolate 4110 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
3.51 3
Compound: PMEA, Adefovir
Antiviral activity against HIV1 clade B isolate 2101 infected in human H9 cells assessed as inhibition of viral replication
Antiviral activity against HIV1 clade B isolate 2101 infected in human H9 cells assessed as inhibition of viral replication
[PMID: 21803462]
H9 EC50
7.9 3
Compound: PMEA, Adefovir
Antiviral activity against 6250 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
Antiviral activity against 6250 TCID50 wild type HIV1 LAI infected in human H9 cells assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
[PMID: 21803462]
HEK-293T CC50
> 100 3
Compound: PMEA
Cytotoxicity against human 293T cells assessed as inhibition of cell proliferation by tetrazolium dye method
Cytotoxicity against human 293T cells assessed as inhibition of cell proliferation by tetrazolium dye method
[PMID: 17470654]
HEL EC50
0.035 2
Compound: PMEA
Antiviral activity against 07/1 strain of VZV in HEL (human erythroleukemia) cells.
Antiviral activity against 07/1 strain of VZV in HEL (human erythroleukemia) cells.
[PMID: 14584956]
HEL EC50
0.03 2
Compound: PMEA
Antiviral activity against OKA strain of VZV in HEL (human erythroleukemia) cells.
Antiviral activity against OKA strain of VZV in HEL (human erythroleukemia) cells.
[PMID: 14584956]
HEL EC50
0.1 2
Compound: PMEA
Antiviral activity against AD169 strain of cytomegalovirus (CMV) in HEL (human erythroleukemia) cells.
Antiviral activity against AD169 strain of cytomegalovirus (CMV) in HEL (human erythroleukemia) cells.
[PMID: 14584956]
HEL EC50
0.27 2
Compound: PMEA
Antiviral activity against Davis strain of cytomegalovirus (CMV) in HEL (human erythroleukemia) cells.
Antiviral activity against Davis strain of cytomegalovirus (CMV) in HEL (human erythroleukemia) cells.
[PMID: 14584956]
HEL EC50
10 6
Compound: PMEA (adefovir)
Inhibition of Thymidine kinase deficient (TK-) Varicella-Zoster virus (VZV) 07/1 strain induced cytopathicity n HEL cell line
Inhibition of Thymidine kinase deficient (TK-) Varicella-Zoster virus (VZV) 07/1 strain induced cytopathicity n HEL cell line
[PMID: 11960502]
HEL EC50
10 6
Compound: PMEA (adefovir)
Inhibition of Thymidine kinase deficient (TK-) Varicella-Zoster virus (VZV) YS/R strain induced cytopathicity in HEL cell line
Inhibition of Thymidine kinase deficient (TK-) Varicella-Zoster virus (VZV) YS/R strain induced cytopathicity in HEL cell line
[PMID: 11960502]
HEL EC50
10 6
Compound: PMEA (adefovir)
Inhibition of Varicella-Zoster virus (VZV) OKA strain induced cytopathicity in HEL cell line
Inhibition of Varicella-Zoster virus (VZV) OKA strain induced cytopathicity in HEL cell line
[PMID: 11960502]
HEL EC50
10 6
Compound: PMEA (adefovir)
Inhibition of Varicella-Zoster virus (VZV) YS strain induced cytopathicity in HEL cell line
Inhibition of Varicella-Zoster virus (VZV) YS strain induced cytopathicity in HEL cell line
[PMID: 11960502]
HEL EC50
114.6 3
Compound: 1, PMEA, Adefovir
Antiviral activity against Human cytomegalovirus Davis infected in HEL cells assessed as protection against virus-induced cytopathicity
Antiviral activity against Human cytomegalovirus Davis infected in HEL cells assessed as protection against virus-induced cytopathicity
[PMID: 21565516]
HEL EC50
117.6 3
Compound: 1, PMEA, Adefovir
Antiviral activity against Human cytomegalovirus AD169 infected in HEL cells assessed as protection against virus-induced cytopathicity
Antiviral activity against Human cytomegalovirus AD169 infected in HEL cells assessed as protection against virus-induced cytopathicity
[PMID: 21565516]
HEL EC50
128 6
Compound: PMEA
Antiviral activity against foscarnet-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against foscarnet-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 18707089]
HEL EC50
137 6
Compound: PMEA
Antiviral activity against acyclovir-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against acyclovir-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 18707089]
HEL EC50
18 6
Compound: PMEA
Antiviral activity against (S)-3-hydroxy-2-phosphonomethoxypropyl cytosine-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against (S)-3-hydroxy-2-phosphonomethoxypropyl cytosine-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 18707089]
HEL EC50
20 3
Compound: PMEA, Adefovir
Antiviral activity against Herpes simplex virus type 2 G infected in HEL cells assessed as inhibition of virus-induced cytopathic effect
Antiviral activity against Herpes simplex virus type 2 G infected in HEL cells assessed as inhibition of virus-induced cytopathic effect
[PMID: 21803462]
HEL 299 CC50
211 3
Compound: 3a, PMEA
Cytotoxicity against HEL299 cells after 4 days by Z1 Coulter counting analysis
Cytotoxicity against HEL299 cells after 4 days by Z1 Coulter counting analysis
[PMID: 17893157]
HEL EC50
20 3
Compound: PMEA, Adefovir
Antiviral activity against TK-deficient and ACR-resistant Herpes simplex virus type 1 KOS infected in HEL cells assessed as inhibition of virus-induced cytopathic effect
Antiviral activity against TK-deficient and ACR-resistant Herpes simplex virus type 1 KOS infected in HEL cells assessed as inhibition of virus-induced cytopathic effect
[PMID: 21803462]
HEL 299 EC50
>183 3
Compound: 3a, PMEA
Antiviral activity against Camelpox virus CML1 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
Antiviral activity against Camelpox virus CML1 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
[PMID: 17893157]
HEL EC50
20 6
Compound: PMEA
Antiviral activity against HCMV 521 with U97 and DNA polymerase mutation in HEL cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against HCMV 521 with U97 and DNA polymerase mutation in HEL cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 18707089]
HeLa CC50
>250 3
Compound: 1, PMEA, Adefovir
Cytotoxicity against human HeLa cells assessed as growth inhibition after 3 days by coulter counting analysis
Cytotoxicity against human HeLa cells assessed as growth inhibition after 3 days by coulter counting analysis
[PMID: 21565516]
HEL EC50
24.9 3
Compound: 1, PMEA, Adefovir
Antiviral activity against Human herpesvirus 2 G infected in HEL cells assessed as protection against virus-induced cytopathicity
Antiviral activity against Human herpesvirus 2 G infected in HEL cells assessed as protection against virus-induced cytopathicity
[PMID: 21565516]
HEL EC50
4.7 3
Compound: 1, PMEA
Antiviral activity against Herpes simplex virus KOS infected in HEL cells assessed as inhibition of virus-induced cytopathicity
Antiviral activity against Herpes simplex virus KOS infected in HEL cells assessed as inhibition of virus-induced cytopathicity
[PMID: 24686012]
HeLa IC50
181 3
Compound: 1, PMEA
Cytostatic activity against human HeLa cells after 72 hrs by coulter counting analysis
Cytostatic activity against human HeLa cells after 72 hrs by coulter counting analysis
[PMID: 24686012]
HepG2 CC50
203 3
Compound: adefovir
Cytotoxicity against HepG2.2.15 cells
Cytotoxicity against HepG2.2.15 cells
[PMID: 16854087]
HEL EC50
41.4 3
Compound: 1, PMEA, Adefovir
Antiviral activity against acyclovir-resistant Human herpesvirus 1 KOS infected in HEL cells assessed as protection against virus-induced cytopathicity
Antiviral activity against acyclovir-resistant Human herpesvirus 1 KOS infected in HEL cells assessed as protection against virus-induced cytopathicity
[PMID: 21565516]
HepG2 EC50
2 3
Compound: PMEA
Compound tested for anti-HBV (hepatitis B virus) activity in HepG2 2.2.15 cell line
Compound tested for anti-HBV (hepatitis B virus) activity in HepG2 2.2.15 cell line
[PMID: 15139764]
HEL EC50
42.5 3
Compound: 1, PMEA, Adefovir
Antiviral activity against Human herpesvirus 1 KOS infected in HEL cells assessed as protection against virus-induced cytopathicity
Antiviral activity against Human herpesvirus 1 KOS infected in HEL cells assessed as protection against virus-induced cytopathicity
[PMID: 21565516]
HepG2 IC50
42.1 3
Compound: PMEA, 1
Antiviral activity against Hepatitis B virus infected human HepG2 cells after 9 days by MTT assay
Antiviral activity against Hepatitis B virus infected human HepG2 cells after 9 days by MTT assay
[PMID: 17888662]
HEL EC50
42 6
Compound: PMEA
Antiviral activity against HCMV 530 with U97 and DNA polymerase mutation in HEL cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against HCMV 530 with U97 and DNA polymerase mutation in HEL cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 18707089]
HepG2 2.2.15 CC50
57 3
Compound: adefovir
Cytotoxicity against HepG2.2.15 cells after 6 hrs by MTT assay
Cytotoxicity against HepG2.2.15 cells after 6 hrs by MTT assay
[PMID: 17499889]
HEL EC50
5 3
Compound: 1, PMEA, Adefovir
Antiviral activity against VZV 07/1 infected in HEL cells assessed as protection against virus-induced cytopathicity
Antiviral activity against VZV 07/1 infected in HEL cells assessed as protection against virus-induced cytopathicity
[PMID: 21565516]
HepG2 2.2.15 CC50
540 3
Compound: adefovir
Cytotoxicity against human HepG2(2.2.15) cells
Cytotoxicity against human HepG2(2.2.15) cells
[PMID: 20000776]
HEL EC50
5.8 6
Compound: PMEA
Antiviral activity against ganciclovir-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against ganciclovir-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 18707089]
HepG2 2.2.15 CC50
540 3
Compound: Adefovir
Cytotoxicity against human HepG2(2.2.15) cells compound treated for 48 hrs followed by incubation for 9 days by MTT assay
Cytotoxicity against human HepG2(2.2.15) cells compound treated for 48 hrs followed by incubation for 9 days by MTT assay
[PMID: 23353737]
HEL EC50
6.3 3
Compound: 1, PMEA
Antiviral activity against Herpes simplex virus G infected in HEL cells assessed as inhibition of virus-induced cytopathicity
Antiviral activity against Herpes simplex virus G infected in HEL cells assessed as inhibition of virus-induced cytopathicity
[PMID: 24686012]
HepG2 2.2.15 CC50
490 3
Compound: Adefovir
Cytotoxicity against human HepG2.2.15 cells assessed as cell death after 9 days by MTS assay
Cytotoxicity against human HepG2.2.15 cells assessed as cell death after 9 days by MTS assay
[PMID: 25650312]
HEL EC50
6.7 3
Compound: 1, PMEA, Adefovir
Antiviral activity against VZV OKA infected in HEL cells assessed as protection against virus-induced cytopathicity
Antiviral activity against VZV OKA infected in HEL cells assessed as protection against virus-induced cytopathicity
[PMID: 21565516]
HEL EC50
7 3
Compound: 1, PMEA
Antiviral activity against thymidine kinase-deficient acyclovir-resistant Herpes simplex virus KOS infected in HEL cells assessed as inhibition of virus-induced cytopathicity
Antiviral activity against thymidine kinase-deficient acyclovir-resistant Herpes simplex virus KOS infected in HEL cells assessed as inhibition of virus-induced cytopathicity
[PMID: 24686012]
HepG2 2.2.15 CC50
200 3
Compound: Adefovir
Cytotoxicity in human HepG2.215 cells assessed as reduction in cell viability after 5 days by CCK8 assay
Cytotoxicity in human HepG2.215 cells assessed as reduction in cell viability after 5 days by CCK8 assay
[PMID: 28082068]
HEL EC50
89 3
Compound: PMEA, Adefovir
Antiviral activity against Herpes simplex virus type 1 KOS infected in HEL cells assessed as inhibition of virus-induced cytopathic effect
Antiviral activity against Herpes simplex virus type 1 KOS infected in HEL cells assessed as inhibition of virus-induced cytopathic effect
[PMID: 21803462]
HepG2 2.2.15 EC50
7.8 3
Compound: Adefovir
Antiviral activity against adefovir-resistant Hepatitis B virus harboring reverse transcriptase N236T mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization meth
Antiviral activity against adefovir-resistant Hepatitis B virus harboring reverse transcriptase N236T mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization meth
[PMID: 21930377]
HEL EC50
9.1 6
Compound: PMEA
Antiviral activity against (S)-3-hydroxy-2-phosphonomethoxypropyl adenine-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against (S)-3-hydroxy-2-phosphonomethoxypropyl adenine-resistant HCMV with DNA polymerase mutant in HEL cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 18707089]
HepG2 2.2.15 EC50
5.5 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
HepG2 2.2.15 EC50
2.1 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M/M204V double mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hyb
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M/M204V double mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hyb
[PMID: 21930377]
HEL EC50
90 6
Compound: PMEA
Antiviral activity against HCMV 6 with U97 mutation in HEL cells assessed as reduction of virus-induced cytopathogenicity
Antiviral activity against HCMV 6 with U97 mutation in HEL cells assessed as reduction of virus-induced cytopathogenicity
[PMID: 18707089]
HepG2 2.2.15 EC50
1.9 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204I mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204I mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
HEL EC50
> 0.17 2
Compound: PMEA
Antiviral activity against vaccinia virus in HEL (human erythroleukemia) cells.
Antiviral activity against vaccinia virus in HEL (human erythroleukemia) cells.
[PMID: 14584956]
HEL EC50
> 183 3
Compound: 1, PMEA, Adefovir
Antiviral activity against Vaccinia virus infected in HEL cells assessed as protection against virus-induced cytopathicity
Antiviral activity against Vaccinia virus infected in HEL cells assessed as protection against virus-induced cytopathicity
[PMID: 21565516]
HepG2 2.2.15 EC50
1.6 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204V mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204V mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
HepG2 2.2.15 EC50
1.3 3
Compound: Adefovir
Antiviral activity against wild type Hepatitis B virus infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization method
Antiviral activity against wild type Hepatitis B virus infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization method
[PMID: 21930377]
HEL EC50
> 200 3
Compound: PMEA, Adefovir
Antiviral activity against Vaccinia virus infected in HEL cells assessed as inhibition of virus-induced cytopathic effect
Antiviral activity against Vaccinia virus infected in HEL cells assessed as inhibition of virus-induced cytopathic effect
[PMID: 21803462]
HepG2 2.2.15 IC50
286 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg level after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg level after 9 days by ELISA
[PMID: 20000776]
HepG2 2.2.15 IC50
286 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg production after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg production after 9 days by ELISA
[PMID: 23353737]
HepG2 2.2.15 IC50
305 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg level after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg level after 9 days by ELISA
[PMID: 20000776]
HepG2 2.2.15 IC50
305 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg production after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg production after 9 days by ELISA
[PMID: 23353737]
HEL 299 CC50
211 3
Compound: 3a, PMEA
Cytotoxicity against HEL299 cells after 4 days by Z1 Coulter counting analysis
Cytotoxicity against HEL299 cells after 4 days by Z1 Coulter counting analysis
[PMID: 17893157]
HepG2 2.2.15 IC50
0.517 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBV DNA replication after 9 days by PCR
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBV DNA replication after 9 days by PCR
[PMID: 20000776]
HEL 299 EC50
> 183 3
Compound: 3a, PMEA
Antiviral activity against Camelpox virus CML1 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
Antiviral activity against Camelpox virus CML1 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
[PMID: 17893157]
HepG2 2.2.15 IC50
0.517 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of viral replication after 9 days by fluorescence PCR method
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of viral replication after 9 days by fluorescence PCR method
[PMID: 23353737]
HEL 299 EC50
> 183 3
Compound: 3a, PMEA
Antiviral activity against Camelpox virus CML14 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
Antiviral activity against Camelpox virus CML14 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
[PMID: 17893157]
HepG2 2.2.15 IC50
215 3
Compound: Adefovir
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as HBeAg secretion after 9 days by ELISA
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as HBeAg secretion after 9 days by ELISA
[PMID: 25650312]
HeLa CC50
> 250 3
Compound: 1, PMEA, Adefovir
Cytotoxicity against human HeLa cells assessed as growth inhibition after 3 days by coulter counting analysis
Cytotoxicity against human HeLa cells assessed as growth inhibition after 3 days by coulter counting analysis
[PMID: 21565516]
HepG2 2.2.15 IC50
257 3
Compound: Adefovir
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as surface antigen HBsAg secretion after 9 days by ELISA
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as surface antigen HBsAg secretion after 9 days by ELISA
[PMID: 25650312]
HeLa IC50
181 3
Compound: 1, PMEA
Cytostatic activity against human HeLa cells after 72 hrs by coulter counting analysis
Cytostatic activity against human HeLa cells after 72 hrs by coulter counting analysis
[PMID: 24686012]
Huh-7 CC50
>150 3
Compound: PMEA, Adefovir
Cytotoxicity against human HuH7 cells
Cytotoxicity against human HuH7 cells
[PMID: 21803462]
HepG2 CC50
203 3
Compound: adefovir
Cytotoxicity against HepG2.2.15 cells
Cytotoxicity against HepG2.2.15 cells
[PMID: 16854087]
Huh-7 EC50
7.7 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase 236T mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase 236T mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
Huh-7 EC50
1.6 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase L180M mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase L180M mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
HepG2 EC50
2 3
Compound: PMEA
Compound tested for anti-HBV (hepatitis B virus) activity in HepG2 2.2.15 cell line
Compound tested for anti-HBV (hepatitis B virus) activity in HepG2 2.2.15 cell line
[PMID: 15139764]
Huh-7 EC50
1.8 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204I mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204I mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
HepG2 IC50
42.1 3
Compound: PMEA, 1
Antiviral activity against Hepatitis B virus infected human HepG2 cells after 9 days by MTT assay
Antiviral activity against Hepatitis B virus infected human HepG2 cells after 9 days by MTT assay
[PMID: 17888662]
Huh-7 EC50
1.5 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204V mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204V mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
Huh-7 EC50
1.3 3
Compound: adefovir
Antiviral activity against adefovir-resistant wild type HBV in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant wild type HBV in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
Huh-7 EC50
6 3
Compound: PMEA, Adefovir
Antiviral activity against Hepatitis B virus infected in human HuH7 cells assessed as reduction in viral DNA level treated day 3 to day 8 post transfection by real time quantitative PCR analysis
Antiviral activity against Hepatitis B virus infected in human HuH7 cells assessed as reduction in viral DNA level treated day 3 to day 8 post transfection by real time quantitative PCR analysis
[PMID: 21803462]
L1210 IC50
3 3
Compound: 1, PMEA
Cytostatic activity against mouse L1210 cells after 48 hrs by coulter counting analysis
Cytostatic activity against mouse L1210 cells after 48 hrs by coulter counting analysis
[PMID: 24686012]
HepG2 2.2.15 CC50
200 3
Compound: Adefovir
Cytotoxicity in human HepG2.215 cells assessed as reduction in cell viability after 5 days by CCK8 assay
Cytotoxicity in human HepG2.215 cells assessed as reduction in cell viability after 5 days by CCK8 assay
[PMID: 28082068]
HepG2 2.2.15 CC50
490 3
Compound: Adefovir
Cytotoxicity against human HepG2.2.15 cells assessed as cell death after 9 days by MTS assay
Cytotoxicity against human HepG2.2.15 cells assessed as cell death after 9 days by MTS assay
[PMID: 25650312]
HepG2 2.2.15 CC50
540 3
Compound: Adefovir
Cytotoxicity against human HepG2(2.2.15) cells compound treated for 48 hrs followed by incubation for 9 days by MTT assay
Cytotoxicity against human HepG2(2.2.15) cells compound treated for 48 hrs followed by incubation for 9 days by MTT assay
[PMID: 23353737]
HepG2 2.2.15 CC50
540 3
Compound: adefovir
Cytotoxicity against human HepG2(2.2.15) cells
Cytotoxicity against human HepG2(2.2.15) cells
[PMID: 20000776]
HepG2 2.2.15 CC50
57 3
Compound: adefovir
Cytotoxicity against HepG2.2.15 cells after 6 hrs by MTT assay
Cytotoxicity against HepG2.2.15 cells after 6 hrs by MTT assay
[PMID: 17499889]
MT4 CC50
187 3
Compound: PMEA
Compound was evaluated for the concentration required to reduce the viability of MT-4 cells.
Compound was evaluated for the concentration required to reduce the viability of MT-4 cells.
10.1016/0960-894X(95)00585-H
MT4 CC50
>10 3
Compound: 1
Compound was tested for antiviral activity against the MT-4 cell lines infected with HIV-1.
Compound was tested for antiviral activity against the MT-4 cell lines infected with HIV-1.
[PMID: 8960556]
MT4 CC50
187 3
Compound: PMEA
Cytotoxic concentration required to reduce the viability of MT-4 cells
Cytotoxic concentration required to reduce the viability of MT-4 cells
10.1016/0960-894X(95)00208-B
MT4 CC50
144 3
Compound: 2
In vitro cytotoxic concentration against MT-4 cells
In vitro cytotoxic concentration against MT-4 cells
[PMID: 11327587]
MT4 EC50
20 3
Compound: PMEA
Compound was evaluated for the inhibition of HIV-1 induced cytopathic effect in MT-4 cells.
Compound was evaluated for the inhibition of HIV-1 induced cytopathic effect in MT-4 cells.
10.1016/0960-894X(95)00585-H
HepG2 2.2.15 EC50
1.3 3
Compound: Adefovir
Antiviral activity against wild type Hepatitis B virus infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization method
Antiviral activity against wild type Hepatitis B virus infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization method
[PMID: 21930377]
HepG2 2.2.15 EC50
1.6 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204V mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204V mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
MT4 EC50
>10 3
Compound: 1
Compound was tested for antiviral activity against the MT-4 cell lines infected with HIV-1.
Compound was tested for antiviral activity against the MT-4 cell lines infected with HIV-1.
[PMID: 8960556]
HepG2 2.2.15 EC50
1.9 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204I mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase M204I mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
MT4 EC50
22 3
Compound: PMEA
Concentration required to inhibit HIV-1-induced cytopathic effect by 50% in MT-4 cells
Concentration required to inhibit HIV-1-induced cytopathic effect by 50% in MT-4 cells
10.1016/0960-894X(95)00208-B
MT4 EC50
7 3
Compound: 2
In vitro antiviral activity against HIV-1 in MT-4 cells
In vitro antiviral activity against HIV-1 in MT-4 cells
[PMID: 11327587]
HepG2 2.2.15 EC50
2.1 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M/M204V double mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hyb
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M/M204V double mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hyb
[PMID: 21930377]
HepG2 2.2.15 EC50
5.5 3
Compound: Adefovir
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
Antiviral activity against lamivudine-resistant Hepatitis B virus harboring reverse transcriptase L180M mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization me
[PMID: 21930377]
MT4 EC50
7.5 3
Compound: 2
In vitro antiviral activity against HIV-2 in MT-4 cells
In vitro antiviral activity against HIV-2 in MT-4 cells
[PMID: 11327587]
HepG2 2.2.15 EC50
7.8 3
Compound: Adefovir
Antiviral activity against adefovir-resistant Hepatitis B virus harboring reverse transcriptase N236T mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization meth
Antiviral activity against adefovir-resistant Hepatitis B virus harboring reverse transcriptase N236T mutant infected in human HepG2(2.2.15) cells assessed as inhibition of virus replication treated daily for 9 days by quantitative blot hybridization meth
[PMID: 21930377]
MT4 IC50
274 6
Compound: 4
Cellular toxic effect was determined in MT-4 cells
Cellular toxic effect was determined in MT-4 cells
[PMID: 11606136]
HepG2 2.2.15 IC50
0.517 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of viral replication after 9 days by fluorescence PCR method
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of viral replication after 9 days by fluorescence PCR method
[PMID: 23353737]
MT4 IC50
2 3
Compound: PMEA
Compound was evaluated for its ability to Inhibit HIV replication in MT-4 cells
Compound was evaluated for its ability to Inhibit HIV replication in MT-4 cells
10.1016/S0960-894X(01)80206-7
HepG2 2.2.15 IC50
0.517 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBV DNA replication after 9 days by PCR
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBV DNA replication after 9 days by PCR
[PMID: 20000776]
MT4 IC50
6.5 3
Compound: PMEA
Compound was evaluated for its ability to Inhibit HIV replication in MT-4 cells
Compound was evaluated for its ability to Inhibit HIV replication in MT-4 cells
10.1016/S0960-894X(01)80206-7
HepG2 2.2.15 IC50
215 3
Compound: Adefovir
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as HBeAg secretion after 9 days by ELISA
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as HBeAg secretion after 9 days by ELISA
[PMID: 25650312]
MT4 IC50
4.1 6
Compound: 4
Inhibition of cytopathogenicity against human HIV-1(IIIB) in MT-4 cells
Inhibition of cytopathogenicity against human HIV-1(IIIB) in MT-4 cells
[PMID: 11606136]
MT4 IC50
3.8 6
Compound: 4
Inhibition of cytopathogenicity against human HIV-2(LAV-2) in MT-4 cells
Inhibition of cytopathogenicity against human HIV-2(LAV-2) in MT-4 cells
[PMID: 11606136]
HepG2 2.2.15 IC50
257 3
Compound: Adefovir
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as surface antigen HBsAg secretion after 9 days by ELISA
Antiviral activity against hepatitis B viral in human HepG2.2.15 cells assessed as surface antigen HBsAg secretion after 9 days by ELISA
[PMID: 25650312]
HepG2 2.2.15 IC50
286 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg production after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg production after 9 days by ELISA
[PMID: 23353737]
PBMC CC50
>30 3
Compound: PMEA, Adefovir
Cytotoxicity against PAP-activated human PBMC on day 7 by MTT assay
Cytotoxicity against PAP-activated human PBMC on day 7 by MTT assay
[PMID: 21803462]
Vero CC50
>100 3
Compound: 1
Compound was tested for antiviral activity against the Vero cells infected with HSV-1.
Compound was tested for antiviral activity against the Vero cells infected with HSV-1.
[PMID: 8960556]
HepG2 2.2.15 IC50
286 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg level after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBeAg level after 9 days by ELISA
[PMID: 20000776]
Vero CC50
>= 250 3
Compound: PMEA
The lowest concentration of compound producing overt cytotoxicity in virus-free vero cell cultures
The lowest concentration of compound producing overt cytotoxicity in virus-free vero cell cultures
10.1016/0960-894X(95)00208-B
HepG2 2.2.15 IC50
305 3
Compound: Adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg production after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg production after 9 days by ELISA
[PMID: 23353737]
Vero EC50
58 3
Compound: PMEA
Anti-herpes virus activity was evaluated against Herpes simplex virus type 1 (HSV-1,strain HF) grown in Vero cells
Anti-herpes virus activity was evaluated against Herpes simplex virus type 1 (HSV-1,strain HF) grown in Vero cells
10.1016/0960-894X(95)00208-B
HepG2 2.2.15 IC50
305 3
Compound: adefovir
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg level after 9 days by ELISA
Antiviral activity against HBV infected in human HepG2(2.2.15) cells assessed as inhibition of HBsAg level after 9 days by ELISA
[PMID: 20000776]
Huh-7 CC50
> 150 3
Compound: PMEA, Adefovir
Cytotoxicity against human HuH7 cells
Cytotoxicity against human HuH7 cells
[PMID: 21803462]
Vero EC50
69 3
Compound: PMEA
Anti-herpes virus activity was evaluated against Herpes simplex virus type 2 (HSV-2,strain G) grown in Vero cells
Anti-herpes virus activity was evaluated against Herpes simplex virus type 2 (HSV-2,strain G) grown in Vero cells
10.1016/0960-894X(95)00208-B
Vero EC50
38.5 3
Compound: 1
Compound was tested for antiviral activity against the Vero cells infected with HSV-1.
Compound was tested for antiviral activity against the Vero cells infected with HSV-1.
[PMID: 8960556]
Huh-7 EC50
1.3 3
Compound: adefovir
Antiviral activity against adefovir-resistant wild type HBV in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant wild type HBV in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
Vero EC50
32.7 3
Compound: 1
Compound was tested for antiviral activity against the Vero cells infected with HSV-2
Compound was tested for antiviral activity against the Vero cells infected with HSV-2
[PMID: 8960556]
Huh-7 EC50
1.5 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204V mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204V mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
Huh-7 EC50
1.6 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase L180M mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase L180M mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
Vero IC50
119 3
Compound: 1
Concentration that reduced plaque formation by 50% was measured in HSV-2 infected vero cells in vitro
Concentration that reduced plaque formation by 50% was measured in HSV-2 infected vero cells in vitro
[PMID: 8021925]
WI-38 CC50
124.7 3
Compound: PMEA
Cytotoxicity against human WI38 cells by neutral red assay
Cytotoxicity against human WI38 cells by neutral red assay
[PMID: 18285481]
Huh-7 EC50
1.6 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase LM/reverse transcriptase MV double mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase LM/reverse transcriptase MV double mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
Huh-7 EC50
1.8 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204I mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase M204I mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
WI-38 EC50
95.8 3
Compound: PMEA
Antimicrobial activity against BK polyomavirus ATCC VR837 infected in human WI38 cells assessed as reduction in viral titer after 7 days by PCR analysis
Antimicrobial activity against BK polyomavirus ATCC VR837 infected in human WI38 cells assessed as reduction in viral titer after 7 days by PCR analysis
[PMID: 18285481]
Huh-7 EC50
6 3
Compound: PMEA, Adefovir
Antiviral activity against Hepatitis B virus infected in human HuH7 cells assessed as reduction in viral DNA level treated day 3 to day 8 post transfection by real time quantitative PCR analysis
Antiviral activity against Hepatitis B virus infected in human HuH7 cells assessed as reduction in viral DNA level treated day 3 to day 8 post transfection by real time quantitative PCR analysis
[PMID: 21803462]
Huh-7 EC50
7.7 3
Compound: adefovir
Antiviral activity against adefovir-resistant HBV reverse transcriptase 236T mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
Antiviral activity against adefovir-resistant HBV reverse transcriptase 236T mutant in human Huh7 cells after 4 days by intracellular HBV DNA replication assay
[PMID: 19072694]
L1210 IC50
3 3
Compound: 1, PMEA
Cytostatic activity against mouse L1210 cells after 48 hrs by coulter counting analysis
Cytostatic activity against mouse L1210 cells after 48 hrs by coulter counting analysis
[PMID: 24686012]
MRC5 CC50
> 100 3
Compound: 1
Compound was tested for antiviral activity against the MRC-5 cells infected with HSV-1.
Compound was tested for antiviral activity against the MRC-5 cells infected with HSV-1.
[PMID: 8960556]
MRC5 CC50
> 250 3
Compound: PMEA
The lowest concentration of compound producing overt cytotoxicity in virus-free MRC-5 cell cultures
The lowest concentration of compound producing overt cytotoxicity in virus-free MRC-5 cell cultures
10.1016/0960-894X(95)00208-B
MRC5 EC50
29.7 3
Compound: 1
Compound was tested for antiviral activity against the MRC-5 cells infected with HSV-1.
Compound was tested for antiviral activity against the MRC-5 cells infected with HSV-1.
[PMID: 8960556]
MRC5 EC50
33.5 3
Compound: 1
Compound was tested for antiviral activity against the MRC-5 cells infected with HSV-2.
Compound was tested for antiviral activity against the MRC-5 cells infected with HSV-2.
[PMID: 8960556]
MRC5 EC50
36 3
Compound: PMEA
Anti-herpes virus activity was evaluated against human cytomegalovirus (HCMV, strain AD-169) grown in MRC-5 cells
Anti-herpes virus activity was evaluated against human cytomegalovirus (HCMV, strain AD-169) grown in MRC-5 cells
10.1016/0960-894X(95)00208-B
MT2 EC50
1.1 3
Compound: 1, PMEA, Adefovir
Antiviral activity against HIV 1 LAI infected in MT2 cells
Antiviral activity against HIV 1 LAI infected in MT2 cells
[PMID: 21565516]
MT4 CC50
144 3
Compound: 2
In vitro cytotoxic concentration against MT-4 cells
In vitro cytotoxic concentration against MT-4 cells
[PMID: 11327587]
MT4 CC50
187 3
Compound: PMEA
Cytotoxic concentration required to reduce the viability of MT-4 cells
Cytotoxic concentration required to reduce the viability of MT-4 cells
10.1016/0960-894X(95)00208-B
MT4 CC50
187 3
Compound: PMEA
Compound was evaluated for the concentration required to reduce the viability of MT-4 cells.
Compound was evaluated for the concentration required to reduce the viability of MT-4 cells.
10.1016/0960-894X(95)00585-H
MT4 CC50
> 10 3
Compound: 1
Compound was tested for antiviral activity against the MT-4 cell lines infected with HIV-1.
Compound was tested for antiviral activity against the MT-4 cell lines infected with HIV-1.
[PMID: 8960556]
MT4 EC50
20 3
Compound: PMEA
Compound was evaluated for the inhibition of HIV-1 induced cytopathic effect in MT-4 cells.
Compound was evaluated for the inhibition of HIV-1 induced cytopathic effect in MT-4 cells.
10.1016/0960-894X(95)00585-H
MT4 EC50
22 3
Compound: PMEA
Concentration required to inhibit HIV-1-induced cytopathic effect by 50% in MT-4 cells
Concentration required to inhibit HIV-1-induced cytopathic effect by 50% in MT-4 cells
10.1016/0960-894X(95)00208-B
MT4 EC50
7 3
Compound: 2
In vitro antiviral activity against HIV-1 in MT-4 cells
In vitro antiviral activity against HIV-1 in MT-4 cells
[PMID: 11327587]
MT4 EC50
7.5 3
Compound: 2
In vitro antiviral activity against HIV-2 in MT-4 cells
In vitro antiviral activity against HIV-2 in MT-4 cells
[PMID: 11327587]
MT4 EC50
> 10 3
Compound: 1
Compound was tested for antiviral activity against the MT-4 cell lines infected with HIV-1.
Compound was tested for antiviral activity against the MT-4 cell lines infected with HIV-1.
[PMID: 8960556]
MT4 IC50
2 3
Compound: PMEA
Compound was evaluated for its ability to Inhibit HIV replication in MT-4 cells
Compound was evaluated for its ability to Inhibit HIV replication in MT-4 cells
10.1016/S0960-894X(01)80206-7
MT4 IC50
274 6
Compound: 4
Cellular toxic effect was determined in MT-4 cells
Cellular toxic effect was determined in MT-4 cells
[PMID: 11606136]
MT4 IC50
3.8 6
Compound: 4
Inhibition of cytopathogenicity against human HIV-2(LAV-2) in MT-4 cells
Inhibition of cytopathogenicity against human HIV-2(LAV-2) in MT-4 cells
[PMID: 11606136]
MT4 IC50
4.1 6
Compound: 4
Inhibition of cytopathogenicity against human HIV-1(IIIB) in MT-4 cells
Inhibition of cytopathogenicity against human HIV-1(IIIB) in MT-4 cells
[PMID: 11606136]
MT4 IC50
6.5 3
Compound: PMEA
Compound was evaluated for its ability to Inhibit HIV replication in MT-4 cells
Compound was evaluated for its ability to Inhibit HIV replication in MT-4 cells
10.1016/S0960-894X(01)80206-7
PBMC CC50
> 30 3
Compound: PMEA, Adefovir
Cytotoxicity against PAP-activated human PBMC on day 7 by MTT assay
Cytotoxicity against PAP-activated human PBMC on day 7 by MTT assay
[PMID: 21803462]
Vero CC50
> 100 3
Compound: 1
Compound was tested for antiviral activity against the Vero cells infected with HSV-1.
Compound was tested for antiviral activity against the Vero cells infected with HSV-1.
[PMID: 8960556]
Vero CC50
>= 250 3
Compound: PMEA
The lowest concentration of compound producing overt cytotoxicity in virus-free vero cell cultures
The lowest concentration of compound producing overt cytotoxicity in virus-free vero cell cultures
10.1016/0960-894X(95)00208-B
Vero EC50
32.7 3
Compound: 1
Compound was tested for antiviral activity against the Vero cells infected with HSV-2
Compound was tested for antiviral activity against the Vero cells infected with HSV-2
[PMID: 8960556]
Vero EC50
38.5 3
Compound: 1
Compound was tested for antiviral activity against the Vero cells infected with HSV-1.
Compound was tested for antiviral activity against the Vero cells infected with HSV-1.
[PMID: 8960556]
Vero EC50
58 3
Compound: PMEA
Anti-herpes virus activity was evaluated against Herpes simplex virus type 1 (HSV-1,strain HF) grown in Vero cells
Anti-herpes virus activity was evaluated against Herpes simplex virus type 1 (HSV-1,strain HF) grown in Vero cells
10.1016/0960-894X(95)00208-B
Vero EC50
69 3
Compound: PMEA
Anti-herpes virus activity was evaluated against Herpes simplex virus type 2 (HSV-2,strain G) grown in Vero cells
Anti-herpes virus activity was evaluated against Herpes simplex virus type 2 (HSV-2,strain G) grown in Vero cells
10.1016/0960-894X(95)00208-B
Vero IC50
119 3
Compound: 1
Concentration that reduced plaque formation by 50% was measured in HSV-2 infected vero cells in vitro
Concentration that reduced plaque formation by 50% was measured in HSV-2 infected vero cells in vitro
[PMID: 8021925]
WI-38 CC50
124.7 3
Compound: PMEA
Cytotoxicity against human WI38 cells by neutral red assay
Cytotoxicity against human WI38 cells by neutral red assay
[PMID: 18285481]
WI-38 EC50
95.8 3
Compound: PMEA
Antimicrobial activity against BK polyomavirus ATCC VR837 infected in human WI38 cells assessed as reduction in viral titer after 7 days by PCR analysis
Antimicrobial activity against BK polyomavirus ATCC VR837 infected in human WI38 cells assessed as reduction in viral titer after 7 days by PCR analysis
[PMID: 18285481]
体外実験

Studies to elucidate the mechanism of action of Adefovir against herpesvirus replication reveals that the phosphorylation of Adefovir occurred intracellularly and is carried out by host cellular enzymes. The diphosphorylated derivatives of Adefovir targeted the viral DNA polymerase and also acted as DNA chain terminators. Adenylate kinase is shown to be responsible for the first phosphorylation, which was followed by ADP kinase and creatine kinase, forming Adefovir diphosphate[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

体内実験

Unaffected by food, Adefovir achieves 60% oral bioavailability. Its half-life is 12-30 hours and Adefovir undergoes renal excretion without significant metabolites. Adefovir does not substantially affect the cytochrome P450 system[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

臨床実験
分子量

273.19

分子式

C8H12N5O4P

CAS 番号
Appearance

Solid

Color

White to off-white

SMILES

NC1=C2N=CN(CCOCP(O)(O)=O)C2=NC=N1

輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件
Powder -20°C 3 years
In solvent -80°C 6 months
  -20°C 1 month
溶剤 & 溶解度
体外: 

0.1 M NaOH : 10 mg/mL (36.60 mM; ultrasonic and adjust pH to 10 with NaOH)

H2O : < 0.1 mg/mL (insoluble)

DMSO : < 1 mg/mL (insoluble or slightly soluble)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.6605 mL 18.3023 mL 36.6046 mL
5 mM 0.7321 mL 3.6605 mL 7.3209 mL
10 mM 0.3660 mL 1.8302 mL 3.6605 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
=
Concentration
×
Volume
×
Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

一般には略語で表示されます:C1V1 = C2V2

濃度 (開始)

C1

×
体積 (開始)

V1

=
濃度 (終了)

C2

×
体積 (終了)

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

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Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
純度とドキュメンテーション

純度: 99.74%

参考文献

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
0.1 M NaOH 1 mM 3.6605 mL 18.3023 mL 36.6046 mL 91.5114 mL
5 mM 0.7321 mL 3.6605 mL 7.3209 mL 18.3023 mL
10 mM 0.3660 mL 1.8302 mL 3.6605 mL 9.1511 mL
15 mM 0.2440 mL 1.2202 mL 2.4403 mL 6.1008 mL
20 mM 0.1830 mL 0.9151 mL 1.8302 mL 4.5756 mL
25 mM 0.1464 mL 0.7321 mL 1.4642 mL 3.6605 mL
30 mM 0.1220 mL 0.6101 mL 1.2202 mL 3.0504 mL
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  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

質量   濃度   体積   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

一般には略語で表示されます:C1V1 = C2V2

濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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製品名:
Adefovir
製品番号:
HY-B1826
数量:
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