CAS NO: | 635728-49-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
Darunavir ethanolate (TMC114 Ethanolate) is a potentHIVprotease inhibitor used to treat and prevent HIV/AIDS. Darunavir has aKiof 1 nM for wild typeHIV-1protease. |
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IC50& Target |
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体外研究 (In Vitro) |
Darunavir is a broad-spectrum potent inhibitor active against HIV-1 clinical isolates with minimal cytotoxicity. Darunavir forms hydrogen bonds with the conserved main-chain atoms of Asp29 and Asp30 of the protease. These interactions are proposed to be critical for the potency of this compound against HIV isolates that are resistant to multiple protease inhibitors[1]. In anin vitrostudy in MT-2 cells, the potency of darunavir is greater than that of saquinavir, amprenavir, nelfinavir, indinavir, lopinavir and ritonavir. Darunavir is primarily metabolized by the hepatic cytochrome P450 (CYP) enzymes, primarily CYP3A. The ‘boosting’ dose of ritonavir acts an an inhibitor of CYP3A, thereby increasing darunavir bioavailability[2].
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体内研究 (In Vivo) |
Darunavir is effective against wild-type and PI-resistant HIV, and has an oral bioavailability of 37%. It needs to be combined with ritonavir, which increases the bioavailability to 82%[3].
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Clinical Trial |
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分子量 |
593.73 |
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性状 |
Solid |
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Formula |
C29H43N3O8S |
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CAS 号 |
635728-49-3 |
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中文名称 |
达芦那韦乙醇 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : ≥ 50 mg/mL(84.21 mM) *"≥" means soluble, but saturation unknown.
配制储备液
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In Vivo:
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