“angiotensin converting enzyme ace”的搜索结果
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(Z)-9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate. Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase (NtART) inhibitor, which blocks reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV.
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CCR8 抑制剂
ML604086 is a selective CCR8 inhibitor, inhibiting CCL1 binding to CCR8 on circulating T-cells. ML604086 inhibits CCL1 mediated chemotaxis and increases in intracellular Ca2+ concentrations.
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HCV NS5A inhibitor
Ledipasvir acetone is the active pharmaceutical ingredient of Ledipasvir. Ledipasvir is an inhibitor of the hepatitis C virus NS5A, with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon.
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antiviral
BAY41-4109 racemic是BAY41-4109的R-异构体和BAY41-4109的S-异构体的混合物。它抑制HepG2.2.15细胞中的乙型肝炎病毒(HBV)复制,而不影响细胞生长,IC50值为202nM。
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Acetohydroxamic acid是细菌和植物脲酶的有效且不可逆的抑制剂,还用作慢性尿路感染的辅助治疗。
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HIV-1 protease 抑制剂
Nelfinavir是一种有效的口服生物可利用的人类免疫缺陷病毒HIV-1蛋白酶抑制剂(Ki=2 nM ),广泛用于与HIV逆转录酶抑制剂联合治疗HIV感染。
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- Reiko Watanabe, .et al. Development of an In Silico Prediction Model for P-glycoprotein Efflux Potential in Brain Capillary Endothelial Cells toward the Prediction of Brain Penetration, J Med Chem, 2021, Mar 11;64(5):2725-2738 PMID: 33619967
- Yang PM, .et al. p38α/S1P/SREBP2 activation by the SAM-competitive EZH2 inhibitor GSK343 limits its anticancer activity but creates a druggable vulnerability in hepatocellular carcinoma, Am J Cancer Res, 2019, Oct 1;9(10):2120-2139 PMID: 31720078
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HIV fusion 抑制剂
Enfuvirtide Acetate (T-20)是一个36个氨基酸的肽段,对应于gp41(HIV-1包膜蛋白的跨膜亚基)区域。
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Ganciclovir Mono-O-acetate是更昔洛韦衍生物。
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