S85911 |
VICRIVIROC MALEATE |
源叶(MedMol) | 99% |
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- 产品描述: Vicriviroc maleate (SCH-417690 maleate; SCH-D maleate) is a potent, selective, oral bioavailable and CNS penetrated antagonist of CCR5, with a Ki of 2.5 nM, and also inhibits HIV-1 in PBMC cells, with IC90s of 3.3 nM (JrFL), 2.8 nM (ADA-M), 1.8 nM (301657), 4.9 nM (JV1083) and 10 nM (RU 570).
- 靶点: CCR5:2.5 nM (Ki);CCR5;HIV-1;HIV-1 (301657):1.8 nM (IC90, in PBMC cells);HIV-1 (ADA-M):2.8 nM (IC90, in PBMC cells);HIV-1 (JrFL):3.3 nM (IC90, in PBMC cells);HIV-1 (JV1083):4.9 nM (IC90, in PBMC cells);HIV-1 (RU 570):10 nM (IC90, in PBMC cells);HIVProtease;CCR
- 体内研究:
Vicriviroc maleate (SCH-417690 maleate; SCH-D maleate; 10 mg/kg) has good oral availablity in rats and monkeys, with no acute CNS or GI effects in rats
- 参考文献:
1. Tagat JR, et al. Piperazine-based CCR5 antagonists as HIV-1 inhibitors. IV. Discovery of 1-[(4,6-dimethyl-5-pyrimidinyl)carbonyl]- 4-[4-[2-methoxy-1(R)-4-(trifluoromethyl)phenyl]ethyl-3(S)-methyl-1-piperazinyl]- 4-methylpiperidine (Sch-417690/Sch-D), a potent, highly selective, and orally bioavailable CCR5 antagonist. J Med Chem. 2004 May 6;47(10):2405-8. 2. Strizki JM, et al. Discovery and characterization of vicriviroc (SCH 417690), a CCR5 antagonist with potent activity against human immunodeficiency virus type 1. Antimicrob Agents Chemother. 2005 Dec;49(12):4911-9.
- 溶解性: Soluble in DMSO、H2O
- 保存条件: 2-8℃
- 配置溶液浓度参考:
1mg 5mg 10mg 1 mM 1.539 ml 7.696 ml 15.392 ml 5 mM 0.308 ml 1.539 ml 3.078 ml 10 mM 0.154 ml 0.77 ml 1.539 ml 50 mM 0.031 ml 0.154 ml 0.308 ml
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本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:
质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)