Name | (2S)-N-[(2S,3S)-4-[(2S)-2-(tert-butylcarbamoyl)pyrrolidin-1-yl]-3-hydroxy-4-oxo-1-phenylbutan-2-yl]-2-(quinoxaline-2-carbonylamino)butanediamide |
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Synonyms | AHPBA analog |
Description | R-87366 is a water-soluble human immunodeficiency virus (HIV) protease inhibitor. R-87366 has potent inhibitory for HIV protease with a Ki value of 11 nM. R-87366 can be used for the research of anti-human immunodeficiency virus (HIV)[1]. |
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Related Catalog | |
Target |
Ki: 11 nM (HIV protease)[1]. IC90: 0.5 μM (HIV-1IIIB acutely infected cells)[1] |
In Vitro | R-87366 对人类免疫缺陷病毒蛋白酶具有强效抑制作用,Ki 值为 11 nM[1]。 R-87366 对 HIV-1IIIB 急性感染细胞具有活性,IC90 值为 0.5 μM[1]。 R-87366 具有中等水溶性[1]。 R-87366 (0.25 μM; 0.5 μM) 对慢性感染的 Molt-4/HIV-1IIIB 细胞也有活性,并抑制 p55 蛋白水解加工成 p17[1]。 |
References |
Density | 1.311g/cm3 |
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Boiling Point | 1055.5ºC at 760 mmHg |
Molecular Formula | C32H39N7O6 |
Molecular Weight | 617.69500 |
Flash Point | 592.1ºC |
Exact Mass | 617.29600 |
PSA | 208.17000 |
LogP | 3.94070 |
Vapour Pressure | 0mmHg at 25°C |
Index of Refraction | 1.622 |