Home>>Signaling Pathways>> Microbiology & Virology>> Reverse Transcriptase>>Stavudine sodium

Stavudine sodium Sale

(Synonyms: 司他夫定钠; d4T sodium) 目录号 : GC37690

An inhibitor of HIV reverse transcriptase

Stavudine sodium Chemical Structure

Cas No.:134624-73-0

规格 价格 库存 购买数量
100mg
¥675.00
现货
500mg
¥1,440.00
现货

电话:400-920-5774 Email: sales@glpbio.cn

Customer Reviews

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

Description

Stavudine is an inhibitor of HIV reverse transcriptase and a derivative of the nucleoside thymidine .1 It inhibits HIV-1 replication in human peripheral blood mononuclear cells (PBMCs; EC50 = 8.8 nM). Stavudine reduces the synthesis of HIV-specific antigen in MT-4 cells when used at concentrations ranging from 0.1 to 10 ?g/ml and reduces HIV-induced plaque formation in MT-4 cells at 0.05 ?g/ml.2 It reduces plasma- and cell-associated viral load in macaques infected with a highly pathogenic isolate of HIV-2.3 Stavudine induces sustained hind paw mechanical allodynia in a rat model of antiretroviral toxic neuropathy (ATN) when administered at a dose of 75 mg/kg twice weekly for five consecutive doses for a cumulative dose of 375 mg/kg.4 Formulations containing stavudine, in combination with other antiretrovirals, have been used in the treatment of HIV-1 infection.

1.Lin, T.-S., Schinazi, R.F., and Prusoff, W.H.Potent and selective in vitro activity of 3'-deoxythymidin-2'-ene (3'-deoxy-2',3'-didehydrothymidine) against human immunodeficiency virusBiochem. Pharmacol.36(17)2713-2718(1987) 2.Hamamoto, Y., Nakashima, H., Matsui, T., et al.Inhibitory effect of 2',3'-didehydro-2',3'-dideoxynucleosides on infectivity, cytopathic effects, and replication of human immunodeficiency virusAntimicrob. Agents Chemother.31(6)907-910(1987) 3.Watson, A., McClure, J., Ranchalis, J., et al.Early postinfection antiviral treatment reduces viral load and prevents CD4+ cell decline in HIV type 2-infected macaquesAIDS Res. Hum. Retroviruses13(16)1375-1381(1997) 4.Kuo, A., Nicholson, J.R., Corradini, L., et al.Establishment and characterisation of a stavudine (d4T)-induced rat model of antiretroviral toxic neuropathy (ATN) using behavioural and pharmacological methodsInflammopharmacology27(2)387-396(2019)

化学性质

Cas No. 134624-73-0 SDF
别名 司他夫定钠; d4T sodium
Canonical SMILES [O-]C[C@H]1O[C@@H](N2C=C(C)C(NC2=O)=O)C=C1.[Na+]
分子式 C10H11N2NaO4 分子量 246.2
溶解度 Soluble in DMSO 储存条件 Store at -20°C
General tips 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 4.0617 mL 20.3087 mL 40.6174 mL
5 mM 0.8123 mL 4.0617 mL 8.1235 mL
10 mM 0.4062 mL 2.0309 mL 4.0617 mL
  • 摩尔浓度计算器

  • 稀释计算器

  • 分子量计算器

质量
=
浓度
x
体积
x
分子量
 
 
 
*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Glpbio的产品页面获得)批次特异的分子量使用本工具。

计算

动物体内配方计算器 (澄清溶液)

第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
给药剂量 mg/kg 动物平均体重 g 每只动物给药体积 ul 动物数量
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方)
% DMSO % % Tween 80 % saline
计算重置

产品文档

Quality Control & SDS

View current batch: