1. Apoptosis Metabolic Enzyme/Protease Immunology/Inflammation Anti-infection NF-κB Cell Cycle/DNA Damage
  2. HSV Fungal Reactive Oxygen Species (ROS) EBV Antibiotic Apoptosis DNA/RNA Synthesis Drug Metabolite
  3. Vidarabine

Vidarabine  (Synonyms: ビダラビン; Ara-A; Adenine Arabinoside; 9-β-D-Arabinofuranosyladenine)

製品番号: HY-B0277 純度: 98.85%
COA 取扱説明書 Technical Support

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.

商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。

Vidarabine

Vidarabine 構造式

CAS 番号 : 5536-17-4

容量 価格(税別) 在庫状況 数量
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
USD 52 在庫あり
Solution
10 mM * 1 mL in DMSO USD 52 在庫あり
Solid
100 mg $48 在庫あり
500 mg $115 在庫あり
1 g $215 在庫あり
5 g   お問い合わせ  
10 g   お問い合わせ  

* アイテムを追加する前、数量をご選択ください

This product is a controlled substance and not for sale in your territory.

カスタマーレビュー

Based on 7 publication(s) in Google Scholar

Other Forms of Vidarabine:

Top Publications Citing Use of Products

HSV アイソフォーム固有の製品をすべて表示:

Antibiotic アイソフォーム固有の製品をすべて表示:

DNA/RNA Synthesis アイソフォーム固有の製品をすべて表示:

  • 生物活性

  • 純度とドキュメンテーション

  • 参考文献

  • カスタマーレビュー

製品説明

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[1][2][3].

IC50 & Target

HSV-2

11.3 μg/mL (IC50)

HSV-1

9.3 μg/mL (IC50)

Cellular Effect
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]
体外実験

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.

臨床実験
分子量

267.25

分子式

C10H13N5O4

CAS 番号
Appearance

Solid

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

Structure Classification
Initial Source

Streptomyces

輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
溶剤 & 溶解度
体外: 

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)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.7418 mL 18.7091 mL 37.4181 mL
5 mM 0.7484 mL 3.7418 mL 7.4836 mL
10 mM 0.3742 mL 1.8709 mL 3.7418 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, 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.

  • 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

体内:

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.

  • Protocol 1

    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.
  • Protocol 2

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

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
%
DMSO +
+
%
Tween-80 +
%
Saline
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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).
Calculation results:
Working solution concentration: mg/mL
Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).
The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
 If the continuous dosing period exceeds half a month, please choose this protocol carefully.
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.
純度とドキュメンテーション

純度: 99.35%

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, 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
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  • Molarity Calculator

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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
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  • 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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