首页 工具
登录
购物车
Vidarabine

Vidarabine

产品编号 T1506   CAS 5536-17-4
别名: Adenine Arabinoside, 阿糖腺苷, 9-β-D-Arabinofuranosyladenine, Vira-A, Arabinosyladenine, Ara-A

Vidarabine (Adenine Arabinoside) 是从链霉菌分离的核苷类抗生素,能抗单纯性疱疹和水痘-带状疱疹病毒。它对 HSV-1 和 HSV-2 的 IC50值分别为 9.3 μg/ml 和 11.3 μg/ml。

TargetMol的所有产品和服务仅用于科学研究,不能被用于人体,我们也不向个人提供产品和服务。
Vidarabine Chemical Structure
Vidarabine, CAS 5536-17-4
规格 价格/CNY 货期 数量
50 mg ¥ 298 现货
100 mg ¥ 418 现货
200 mg ¥ 671 现货
500 mg ¥ 980 现货
1 mL * 10 mM (in DMSO) ¥ 460 现货
其他形式的 Vidarabine:
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
Venetoclax限时半价
产品目录号及名称: Vidarabine (T1506)
点击图片重新获取验证码
选择批次  
纯度: 100%
更多批次查询请联系客服
天然产物信息
生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 Vidarabine (Adenine Arabinoside) is a nucleoside antibiotic isolated from Streptomyces antibioticus. It has some antineoplastic properties and has broad spectrum activity against DNA viruses in cell cultures and significant antiviral activity against infections caused by a variety of viruses such as the herpes viruses, the VACCINIA VIRUS and varicella zoster virus.
靶点活性 HSV2:11.3 μg/mL (IC50), HSV1:9.3 μg/mL (IC50)
体外活性 Vidarabine and Acyclovir have a synergistic effect on wild type . Vidarabine is capable of inhibiting acyclovir-resistant/TK-deficient mutants of HSV and VZV, because it is phosphorylated to its active vidarabine–triphosphate form by cellular kinases and is not dependent for its activation on the viral TK. [1] Vidarabine and acyclovir (ACV) alone show a concentration-dependent inhibition of plaque formation of HSV-1 in Vero cells. Vidarabine combined with acidic protein bound polysaccharide (APBP) show synergistic effects on the plaque formation of HSV-1 in Vero cells. [2] Vidarabine acts directly on the DNA polymerase of varicella-zoster virus (VZV) and double-strand DNA viruses, including human adenoviruses. Vidarabine specifically inhibits adenovirus type 11 replication without obvious cytotoxicity in vitro. Vidarabine acts less on the synthesis of early proteins but rather on those after DNA replication. [3] Vidarabine is an antiviral drug with activity against herpes viruses, poxviruses, and certain rhabdoviruses, hepadnarviruses, and RNA tumor viruses. Vidarabine also is active against vaccinia virus both in vitro and in vivo. [4]
体内活性 Vidarabine is rapidly deaminated to 9-β-D-arabinofuranosyl hypoxanthine (Ara-Hx) as the principal metabolite. [3]
别名 Adenine Arabinoside, 阿糖腺苷, 9-β-D-Arabinofuranosyladenine, Vira-A, Arabinosyladenine, Ara-A
分子量 267.24
分子式 C10H13N5O4
CAS No. 5536-17-4

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

H2O: 3 mg/mL (11.22 mM)

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

DMSO: 49 mg/mL (183.4 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
H2O / DMSO 1 mM 3.742 mL 18.7098 mL 37.4195 mL 93.5489 mL
5 mM 0.7484 mL 3.742 mL 7.4839 mL 18.7098 mL
10 mM 0.3742 mL 1.871 mL 3.742 mL 9.3549 mL
DMSO 20 mM 0.1871 mL 0.9355 mL 1.871 mL 4.6774 mL
50 mM 0.0748 mL 0.3742 mL 0.7484 mL 1.871 mL
100 mM 0.0374 mL 0.1871 mL 0.3742 mL 0.9355 mL

TargetMol Calculator计算器

摩尔浓度计算器
稀释计算器
配液计算器
分子量计算器
=
X
X
X
=
X
=
/
g/mol

输入分子式,点击计算,可计算出产品的分子量。

TargetMol Library Books参考文献

1. Suzuki M, et al. Antiviral Res, 2006, 72(2), 157-161. 2. Oh KW, et al. J Ethnopharmacol, 2000, 72(1-2), 221-227. 3. Kurosaki K, et al. Antivir Chem Chemother, 2004, 15(5), 281-285. 4. Shen W, et al. Bioorg Med Chem Lett, 2009, 19(3), 792-796.

TargetMol Library Books文献引用

1. Li L, Zhang Y, Chen Z, et al.SIRT1-dependent mitochondrial biogenesis supports therapeutic effects of vidarabine against rotenone-induced neural cell injury.Heliyon.2023
LNA-Adenosine Peldesine (S)-GNA-T-phosphoramidite LY2334737 N6-Bz-5'-O-DMTr-3'-deoxyadenosine-2'-O-CED-phosphoramidite 2’-Deoxy-N4-methylcytidine 5,6-Dihydro-5-methyluracil 5-Aminouridine

相关化合物库

该产品包含在如下化合物库中:
激酶抑制剂库 药物功能重定位化合物库 FDA 上市激酶抑制剂库 抗癌活性化合物库 酪氨酸激酶分子库 抗癌上市药物库 微生物天然产物库 抗癌药物库 毒性化合物库 NO PAINS 化合物库

TargetMol Calculator剂量换算

对于不同动物的给药剂量换算,您也可以参考 更多...

TargetMol Calculator 体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。

母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

第一步:请输入动物实验的基本信息
剂量
mg/kg
每只动物体重
g
给药体积
μL
动物数量
第二步:请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% ddH2O
计算 重置

技术支持

您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。

Keywords

Vidarabine 5536-17-4 Cell Cycle/Checkpoint DNA Damage/DNA Repair Microbiology/Virology Tyrosine Kinase/Adaptors HSV Nucleoside Antimetabolite/Analog Antibiotic Tyrosine Kinases DNA/RNA Synthesis 9-beta-D-Arabinofuranosyladenine Orthopoxvirus Adenine Arabinoside 阿糖腺苷 9-β-D-Arabinofuranosyladenine Inhibitor 9-b-D-Arabinofuranosyladenine Vira-A Arabinosyladenine inhibit Herpes simplex virus Ara-A inhibitor

 

TargetMol Loading
陶术
生物
TargetMol®中国区唯一合作伙伴
点击进入陶术生物官网陶术生物
联系我们
400-820-0310

上海市静安区江场三路238号8楼