Vidarabine
Based on 7 publication(s) in Google Scholar
Vidarabine (Ara-A) is a nucleoside antibiotic isolated from Streptomyces, and a metabolite of Vidarabine phosphate (HY-B0277A). Vidarabine selectively inhibits viral DNA polymerase and cellular ribonucleotide reductase, thereby blocking viral replication. Vidarabine phosphate also exhibits antifungal activity, induces late-stage cellular apoptosis, and causes cell cycle arrest. Vidarabine phosphate can be used in research related to severe chronic active Epstein-Barr virus (EBV) infection, herpes infection, and candidiasis.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- Reinheit: 98.85%
- CAS. Nr.: 5536-17-4
- Formel: C10H13N5O4
- Molecular Weight:267.25
-
Speicherung:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) Vidarabine
More- Signal Transduct Target Ther. 2025 Dec 15;10(1):406. [Abstract]
- Cells. 2022 Oct 11;11(20):3187. [Abstract]
- J Mol Med (Berl). 2019 Aug;97(8):1183-1193. [Abstract]
- J Cell Physiol. 2021 Aug;236(8):5785-5800. [Abstract]
- Int J Biochem Cell Biol. 2022 Aug:149:106247. [Abstract]
- Vet Microbiol. 2026 May:316:110992. [Abstract]
- bioRxiv. 2020 Apr.
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Biologische Aktivität
|
HSV-2 11.3 μg/mL (IC50) |
HSV-1 9.3 μg/mL (IC50) |
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| Caco-2 | IC50 |
62 nM
Compound: ara-A, vidarabine
|
Inhibition of human DPP4 from human Caco-2 cells
Inhibition of human DPP4 from human Caco-2 cells
|
[PMID: 20000418] |
| CCRF-CEM | IC50 |
24.8 μM
Compound: ara A
|
Antitumor activity was evaluated against CEM cell line
Antitumor activity was evaluated against CEM cell line
|
[PMID: 9871764] |
| CCRF-CEM | IC50 |
24.8 μM
Compound: araA
|
Compound was evaluated for its antiproliferative activity on human T-lymphocyte CEM cells
Compound was evaluated for its antiproliferative activity on human T-lymphocyte CEM cells
|
10.1016/S0960-894X(97)00044-9 |
| CCRF-HSB-2 | IC50 |
12.9 μg/mL
Compound: araA
|
Antiproliferative effects on CCRF-HSB-2 (human leukemia) cells.
Antiproliferative effects on CCRF-HSB-2 (human leukemia) cells.
|
[PMID: 9216836] |
| HEL | EC50 |
10 μM
Compound: ara-A, vidarabine
|
Antiviral activity against Vaccinia virus Lederle infected in HEL cells assessed as inhibition of virus-induced cytopathicity in presence of vildagliptin
Antiviral activity against Vaccinia virus Lederle infected in HEL cells assessed as inhibition of virus-induced cytopathicity in presence of vildagliptin
|
[PMID: 20000418] |
| HEL | EC50 |
35 μM
Compound: ara-A, vidarabine
|
Antiviral activity against HSV1 KOS infected in HEL cells assessed as inhibition of virus-induced cytopathicity
Antiviral activity against HSV1 KOS infected in HEL cells assessed as inhibition of virus-induced cytopathicity
|
[PMID: 20000418] |
| HEL | EC50 |
42 μM
Compound: ara-A, vidarabine
|
Antiviral activity against HSV1 KOS infected in HEL cells assessed as inhibition of virus-induced cytopathicity in presence of vildagliptin
Antiviral activity against HSV1 KOS infected in HEL cells assessed as inhibition of virus-induced cytopathicity in presence of vildagliptin
|
[PMID: 20000418] |
| HEL | EC50 |
8.3 μM
Compound: ara-A, vidarabine
|
Antiviral activity against Vaccinia virus Lederle infected in HEL cells assessed as inhibition of virus-induced cytopathicity
Antiviral activity against Vaccinia virus Lederle infected in HEL cells assessed as inhibition of virus-induced cytopathicity
|
[PMID: 20000418] |
| HEL | ED50 |
1.17 μg/mL
Compound: araA
|
Antiviral activity against varicella zoster virus (VZV) Oka strain in HEL (human erythroleukemia) cells.
Antiviral activity against varicella zoster virus (VZV) Oka strain in HEL (human erythroleukemia) cells.
|
[PMID: 9216836] |
| HEL | ED50 |
17.1 μg/mL
Compound: araA
|
Antiviral activity against herpes simplex virus-1 VR-3 strain in HEL (human erythroleukemia) cells.
Antiviral activity against herpes simplex virus-1 VR-3 strain in HEL (human erythroleukemia) cells.
|
[PMID: 9216836] |
| HEL | ED50 |
6.45 μg/mL
Compound: araA
|
Antiviral activity against human cytomegalovirus (HCMV) AD 169 strain HEL (human erythroleukemia) cells.
Antiviral activity against human cytomegalovirus (HCMV) AD 169 strain HEL (human erythroleukemia) cells.
|
[PMID: 9216836] |
| HEL | ED50 |
6.6 μg/mL
Compound: araA
|
Antiviral activity against herpes simplex virus-2 (HSV-2) Ms strain in HEL (human erythroleukemia) cells.
Antiviral activity against herpes simplex virus-2 (HSV-2) Ms strain in HEL (human erythroleukemia) cells.
|
[PMID: 9216836] |
| HFF | CC50 |
>100 μM
Compound: 1
|
Cytotoxicity against HFF
Cytotoxicity against HFF
|
[PMID: 19097789] |
| HFF | CC50 |
90 μM
Compound: 1
|
Cytotoxicity against HFF in presence of deoxy-coformycin
Cytotoxicity against HFF in presence of deoxy-coformycin
|
[PMID: 19097789] |
| HFF | IC50 |
2 μM
Compound: Ara-A
|
Antiviral activity against Vaccinia virus Copenhagen infected in HFF cells assessed as reduction in plaque formation after 3 days
Antiviral activity against Vaccinia virus Copenhagen infected in HFF cells assessed as reduction in plaque formation after 3 days
|
[PMID: 21641218] |
| HL-60 | IC50 |
20.9 μg/mL
Compound: ara-A
|
The cytotoxic activity in HL-60 cells
The cytotoxic activity in HL-60 cells
|
[PMID: 9371251] |
| KB | IC50 |
39 μg/mL
Compound: ara-A
|
In vitro cytotoxicity against herpes simplex virus type-1 (HSV-1) HF strain in infected KB cells
In vitro cytotoxicity against herpes simplex virus type-1 (HSV-1) HF strain in infected KB cells
|
[PMID: 2838633] |
| KB | IC50 |
5.6 μg/mL
Compound: ara-A
|
Inhibitory activity against herpes simplex virus type-1 (HSV-1) replication in KB cells
Inhibitory activity against herpes simplex virus type-1 (HSV-1) replication in KB cells
|
[PMID: 2838633] |
| L1210 | IC50 |
14.2 μM
Compound: ara A
|
Antitumor activity was evaluated against L1210 cell line
Antitumor activity was evaluated against L1210 cell line
|
[PMID: 9871764] |
| L1210 | IC50 |
14.2 μM
Compound: araA
|
Tested for its antiproliferative activity on murine leukemia L1210 cells
Tested for its antiproliferative activity on murine leukemia L1210 cells
|
10.1016/S0960-894X(97)00044-9 |
| MOLT-4 | IC50 |
11.9 μM
Compound: ara A
|
Antitumor activity was evaluated against Molt4/C8 cell line
Antitumor activity was evaluated against Molt4/C8 cell line
|
[PMID: 9871764] |
| MOLT-4 | IC50 |
11.9 μM
Compound: araA
|
Compound was evaluated for its antiproliferative activity on human T-lymphocyte Molt4/C8 cells
Compound was evaluated for its antiproliferative activity on human T-lymphocyte Molt4/C8 cells
|
10.1016/S0960-894X(97)00044-9 |
| PRK | IC50 |
0.4 μg/mL
Compound: ara-A
|
Compound was evaluated for antiviral activity in rabbit kidney cells infected with vaccinia virus
Compound was evaluated for antiviral activity in rabbit kidney cells infected with vaccinia virus
|
[PMID: 6267280] |
| PRK | IC50 |
1 μg/mL
Compound: ara-A
|
Concentration required to reduce HSV-1(KOS) induced cytopathogenicity by 50% was measured by the addition of [1,'2'-3H]dUrd
Concentration required to reduce HSV-1(KOS) induced cytopathogenicity by 50% was measured by the addition of [1,'2'-3H]dUrd
|
[PMID: 6267280] |
| PRK | IC50 |
1 μg/mL
Compound: ara-A
|
Concentration required to reduce HSV-1(KOS) induced cytopathogenicity by 50% was measured by the addition of [Me-3H]-dThd
Concentration required to reduce HSV-1(KOS) induced cytopathogenicity by 50% was measured by the addition of [Me-3H]-dThd
|
[PMID: 6267280] |
| PRK | IC50 |
10 μg/mL
Compound: ara-A
|
Concentration required to inhibit incorporation of [1,'2'-3H]dUrd into DNA of primary rabbit kidney (PRK) cells by 50%
Concentration required to inhibit incorporation of [1,'2'-3H]dUrd into DNA of primary rabbit kidney (PRK) cells by 50%
|
[PMID: 6267280] |
| PRK | IC50 |
10 μg/mL
Compound: ara-A
|
Concentration required to reduce TK-HSV-1 (B2006) induced cytopathogenicity by 50% in primary rabbit kidney (PRK) cells
Concentration required to reduce TK-HSV-1 (B2006) induced cytopathogenicity by 50% in primary rabbit kidney (PRK) cells
|
[PMID: 6267280] |
| PRK | IC50 |
20 μg/mL
Compound: ara-A
|
Concentration required to inhibit incorporation of [Me-3H]-dThd into DNA of primary rabbit kidney (PRK) cells by 50%
Concentration required to inhibit incorporation of [Me-3H]-dThd into DNA of primary rabbit kidney (PRK) cells by 50%
|
[PMID: 6267280] |
| PRK | IC50 |
3 μg/mL
Compound: ara-A
|
Concentration required to reduce HSV-2 induced cytopathogenicity by 50% in primary rabbit kidney (PRK) cells; 2-4
Concentration required to reduce HSV-2 induced cytopathogenicity by 50% in primary rabbit kidney (PRK) cells; 2-4
|
[PMID: 6267280] |
| PRK | IC50 |
4 μg/mL
Compound: ara-A
|
Concentration required to reduce HSV-1(KOS) induced cytopathogenicity by 50% was measured
Concentration required to reduce HSV-1(KOS) induced cytopathogenicity by 50% was measured
|
[PMID: 6267280] |
| PRK | IC50 |
7 μg/mL
Compound: ara-A
|
Concentration required to reduce HSV-1 induced cytopathogenicity by 50% in primary rabbit kidney (PRK) cells; 4-10
Concentration required to reduce HSV-1 induced cytopathogenicity by 50% in primary rabbit kidney (PRK) cells; 4-10
|
[PMID: 6267280] |
| Vero | CC50 |
38 μM
Compound: araA
|
Cytotoxicity against african green monkey Vero cells after 2 days
Cytotoxicity against african green monkey Vero cells after 2 days
|
[PMID: 17438061] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against HSV1 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against HSV1 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against HSV2 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against HSV2 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate A1 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate A1 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate A2 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate A2 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate A3 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate A3 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate A4 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate A4 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate A5 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate A5 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate A6 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate A6 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate E2490 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate E2490 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MC1 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MC1 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MC2 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MC2 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MJ1 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MJ1 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MJ2 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MJ2 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MJ3 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MJ3 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MP1 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MP1 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR1 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR1 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR10 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR10 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR11 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR11 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR2 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR2 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR3 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR3 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR4 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR4 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR5 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR5 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR6 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR6 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR7 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR7 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR8 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR8 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
26.5 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate MR9 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate MR9 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
28 μM
Compound: araA
|
Antiviral activity against Herpes B virus 24105 infected in african green monkey Vero cells assessed as plaque reduction after 36 to 48 hrs
Antiviral activity against Herpes B virus 24105 infected in african green monkey Vero cells assessed as plaque reduction after 36 to 48 hrs
|
[PMID: 17438061] |
| Vero | EC50 |
35 μM
Compound: araA
|
Antiviral activity against Herpes B virus 32425 infected in african green monkey Vero cells assessed as plaque reduction after 36 to 48 hrs
Antiviral activity against Herpes B virus 32425 infected in african green monkey Vero cells assessed as plaque reduction after 36 to 48 hrs
|
[PMID: 17438061] |
| Vero | EC50 |
37.8 μM
Compound: VDB
|
Antiviral activity against thymidine kinase deficient Macacine herpesvirus 1 isolate E2490 infected in african green monkey Vero cells by plaque reduction assay
Antiviral activity against thymidine kinase deficient Macacine herpesvirus 1 isolate E2490 infected in african green monkey Vero cells by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
46.1 μM
Compound: VDB
|
Antiviral activity against Macacine herpesvirus 1 isolate E2490 infected in african green monkey Vero cells harboring stop mutation thymidine kinase by plaque reduction assay
Antiviral activity against Macacine herpesvirus 1 isolate E2490 infected in african green monkey Vero cells harboring stop mutation thymidine kinase by plaque reduction assay
|
[PMID: 19858259] |
| Vero | EC50 |
7 μM
Compound: araA
|
Antiviral activity against Herpes simplex virus 1 F infected in african green monkey Vero cells assessed as plaque reduction after 36 to 48 hrs
Antiviral activity against Herpes simplex virus 1 F infected in african green monkey Vero cells assessed as plaque reduction after 36 to 48 hrs
|
[PMID: 17438061] |
Vidarabine (18-1200 μg/mL; 48 h) exhibits bactericidal activity against Candida albicans, with an MIC50 and MFC of 150 μg/mL and 300 μg/mL, respectively[3].
Vidarabine (150-300 μg/mL; 4-24 h) induces intracellular ROS accumulation, nuclear pyknosis, late-stage apoptosis and cell cycle arrest in Candida albicans cells, and reduces their ergosterol content[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
-
CAS. Nr. 5536-17-4
-
Appearance Solid
-
Molecular Weight 267.25
-
Formel C10H13N5O4
-
Color White to off-white
-
SMILES
OC[C@@H]1[C@@H](O)[C@H](O)[C@H](N2C3=NC=NC(N)=C3N=C2)O1
-
Synonyms
Ara-A; Adenine Arabinoside; 9-β-D-Arabinofuranosyladenine
-
Structure Classification
-
Initial Source
Streptomyces
-
Versand
Room temperature in continental US; may vary elsewhere.
-
Speicherung
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (7)
-
Journal Impact Factor
-
Most Recent
-
Signal Transduct Target Ther
Selective depletion of tumor-associated SAMHD1 enhances chemotherapeutic efficacy and antitumor immune responses. [Abstract]2025 Dec 15;10(1):406. PMID: 41392286 -
Cells
2022 Oct 11;11(20):3187. PMID: 36291055 -
J Mol Med (Berl)
2019 Aug;97(8):1183-1193. PMID: 31201471 -
J Cell Physiol
C1q/tumor necrosis factor-related protein-6 attenuates TNF-α-induced apoptosis in salivary acinar cells via AMPK/SIRT1-modulated miR-34a-5p expression. [Abstract]2021 Aug;236(8):5785-5800. PMID: 33400820 -
Int J Biochem Cell Biol
C1q/tumour necrosis factor-related protein-3 alleviates high-glucose-induced lipid accumulation and necroinflammation in renal tubular cells by activating the adenosine monophosphate-activated protein kinase pathway. [Abstract]2022 Aug:149:106247. PMID: 35753650 -
Vet Microbiol
The Chinese medicine monomer Schisandrin C inhibits PRRSV infection by regulating the OGT-PI3K/AKT/mTOR signaling pathway. [Abstract]2026 May:316:110992. PMID: 41865607 -
Lösungsmittel & Löslichkeit
DMSO : 50 mg/mL (187.09 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
H2O : < 0.1 mg/mL (insoluble)
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (9.35 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (9.35 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
Please enter the basic information of animal experiments:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
-
%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
-
%+
-
+%Tween-80 + +
-
%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Reinheit & Dokumentation
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Data Sheet (279 KB)
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SDS (419 KB)
- English - EN (419 KB)
- Français - FR (419 KB)
- Deutsch - DE (419 KB)
- Norwegian - NO (419 KB)
- Español - ES (419 KB)
- Swedish - SV (419 KB)
- Italian - IT (419 KB)
- Portuguese - PT (419 KB)
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Handling Instructions (2659 KB)
Verweise
[1]. Kimura H, et al. Vidarabine therapy for severe chronic active Epstein-Barr virus infection. J Pediatr Hematol Oncol. 2001;23(5):294-299. [Content Brief]
[3]. Gavandi TC, et al. Vidarabine as a novel antifungal agent against Candida albicans: insights on mechanism of action. Int Microbiol. 2025;28(3):589-602. [Content Brief]
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 3.7418 mL | 18.7091 mL | 37.4181 mL | 93.5454 mL |
| 5 mM | 0.7484 mL | 3.7418 mL | 7.4836 mL | 18.7091 mL | |
| 10 mM | 0.3742 mL | 1.8709 mL | 3.7418 mL | 9.3545 mL | |
| 15 mM | 0.2495 mL | 1.2473 mL | 2.4945 mL | 6.2364 mL | |
| 20 mM | 0.1871 mL | 0.9355 mL | 1.8709 mL | 4.6773 mL | |
| 25 mM | 0.1497 mL | 0.7484 mL | 1.4967 mL | 3.7418 mL | |
| 30 mM | 0.1247 mL | 0.6236 mL | 1.2473 mL | 3.1182 mL | |
| 40 mM | 0.0935 mL | 0.4677 mL | 0.9355 mL | 2.3386 mL | |
| 50 mM | 0.0748 mL | 0.3742 mL | 0.7484 mL | 1.8709 mL | |
| 60 mM | 0.0624 mL | 0.3118 mL | 0.6236 mL | 1.5591 mL | |
| 80 mM | 0.0468 mL | 0.2339 mL | 0.4677 mL | 1.1693 mL | |
| 100 mM | 0.0374 mL | 0.1871 mL | 0.3742 mL | 0.9355 mL |