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Fosamprenavir Calcium Salt

Fosamprenavir Calcium Salt

产品编号 T8238   CAS 226700-81-8
别名: 福沙那伟钙, Diallyl Trisulfide, GW433908G

Fosamprenavir Calcium Salt (GW433908G) 是抗逆转录病毒蛋白酶抑制剂 Amprenavir 的磷酸酯前药,具有改善的溶解性和抗HIV 感染作用。

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Fosamprenavir Calcium Salt Chemical Structure
Fosamprenavir Calcium Salt, CAS 226700-81-8
规格 价格/CNY 货期 数量
1 mg ¥ 543 现货
2 mg ¥ 795 现货
5 mg ¥ 1,330 现货
10 mg ¥ 1,970 现货
25 mg ¥ 3,350 现货
50 mg ¥ 4,650 现货
100 mg ¥ 6,660 现货
其他形式的 Fosamprenavir Calcium Salt:
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
产品目录号及名称: Fosamprenavir Calcium Salt (T8238)
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纯度: 99.59%
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生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 Fosamprenavir Calcium Salt (GW433908G) (GW433908G) is a phosphate ester prodrug of the antiretroviral protease inhibitor Amprenavir, with improved solubility. Fosamprenavir Calcium Salt has Anti-HIV infection.
体内活性 Oral gavage of DATS significantly retarded growth of PC-3 xenografts in athymic mice without causing weight loss. For instance, 20 days after starting therapy, the average tumor volume in control mice was approximately 3-fold higher compared with DATS-treated mice. Tumors from DATS-treated mice exhibited a markedly higher count of apoptotic bodies compared with control tumors. Consistent with the results in cultured PC-3 cells, the DATS-mediated suppression of PC-3 xenograft growth correlated with induction of proapoptotic proteins Bax and Bak. Although DATS treatment inhibited migration of cultured PC-3 cells in association with down-regulation of vascular endothelial growth factor receptor-2 protein, formation of new blood vessels was comparable in tumors of control and DATS-treated mice as judged by CD31 immunostaining[1].
动物实验 DATS was given orally (6 micromoL, thrice weekly) to male athymic mice s.c. implanted with PC-3 cells. Tumor sections from control and DATS-treated mice were examined for apoptotic bodies by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling assay. Protein levels of apoptosis and cell cycle regulating proteins in tumor tissues of control and DATS-treated mice were determined by immunoblotting. The effect of DATS treatment on in vivo angiogenesis was determined by immunohistochemical analysis of CD31 in tumors[1].
别名 福沙那伟钙, Diallyl Trisulfide, GW433908G
分子量 623.67
分子式 C25H34CaN3O9PS
CAS No. 226700-81-8

存储

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

溶解度

DMSO: 1.8 mg/mL (2.89 mM), Sonification and heating are recommended.

H2O: 0.25 mg/mL (0.40 mM), Sonification and heating are recommended.

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.6034 mL 8.0171 mL 16.0341 mL 40.0853 mL

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TargetMol Library Books参考文献

1. Falcoz C, et al. Pharmacokinetics of GW433908, a prodrug of amprenavir, in healthy male volunteers. J Clin Pharmacol. 2002 Aug;42(8):887-98. 2. Michael P , Silvia S . Dietary Bioactive Diallyl Trisulfide in Cancer Prevention and Treatment[J]. International Journal of Molecular Sciences, 2017, 18(8):1645-. 3. Xiao D , Lew K L , Kim Y A , et al. Diallyl Trisulfide Suppresses Growth of PC-3 Human Prostate Cancer Xenograft In vivo in Association with Bax and Bak Induction[J]. Clinical Cancer Research, 2006, 12(22):6836-6843.
Peldesine BI 224436 CDK9-IN-30 Ditiocarb sodium Shikonin Lamivudine Stavudine Vesnarinone

相关化合物库

该产品包含在如下化合物库中:
抑制剂库 EMA 上市药物库 药物功能重定位化合物库 FDA上市及药典收录分子库 FDA 上市药物库 上市药物库 抗病毒库 已知活性化合物库 经典已知活性库 共价抑制剂库

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
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% ddH2O
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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

Fosamprenavir Calcium Salt 226700-81-8 Microbiology/Virology Proteases/Proteasome HIV Protease Human immunodeficiency virus HIV Inhibitor 福沙那伟钙 Diallyl Diallyl Trisulfide GW433908G inhibit inhibitor

 

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