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Amprenavir

品牌 厂商性质 产地 货期
阿拉丁 生产商 上海 现货

询价
产品参数
货号 CAS号 操作
A124983-250mg 161814-49-9 询价
A124983-25mg 161814-49-9 询价
A124983-50mg 161814-49-9 询价
A124983-5mg 161814-49-9 询价
产品介绍

  • 分子式 C25H35N3O6S
  • 分子量505.63
  • Beilstein号
  • EC号
  • MDL号
  • PubChem编号

属性

敏感性 易吸湿
溶解性
  • DMSO 16 mg/mL
  • Water <1 mg/mL
  • Ethanol 101 mg/mL
  • 存贮条件 储存温度-20°C

    描述

    产品介绍 Amprenavir is a second-generation drug derived from hydroxyethylamine sulfonamide.
    备注 Amprenavir is an HIV protease inhibitor with IC50 of 14.6 ng/mL in wild-type HIV isolates.
    生化机理

    Description:
    IC50 Value: 0.6nM (Ki); Against wild-type clinical HIV isolates:14.6 +/- 12.5 ng/mL (mean +/- SD) [1].
    Amprenavir (Agenerase, GlaxoSmithKline) is a HIV protease inhibitor used to treat HIV infection. It was approved by the Food and Drug Administration on April 15, 1999, for twice-a-day dosing instead of needing to be taken every eight hours.
    in vitro: Amprenavir has an enzyme inhibition constant (Ki = 0.6 nM) that falls within the Ki range of the other protease inhibitors. Amprenavir's in vitro 50% inhibitory concentration (IC50) against wild-type clinical HIV isolates is 14.6 +/- 12.5 ng/mL (mean +/- SD) [1]. Amprenavir had direct inhibitory effects on invasion of Huh-7 hepatocarcinoma cell lines, inhibiting MMP proteolytic activation [2].
    in vivo: Amprenavir was able to promote regression of hepatocarcinoma growth in vivo by anti-angiogenetic and overall anti-tumor activities, independently by PI3K/AKT related pathways that at tod

    别名 Agenerase;;Agenerase;N-[(1S,2R)-3-[[(4-Aminophenyl)sulfonyl](2-methylpropyl)amino]-2-hydroxy-1-(phenylmethyl)propyl]carbamic acid (3S)-tetrahydro-3-furanyl ester; VX-478;

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    注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途