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| Product | Description | |
|---|---|---|
| BMS-955176 | BMS-955176 is the second generation HIV-1 maturation inhibitor. Synonyms: BMS-955176 free base|BMS-955176|UNII-4CA9IAU7RJ|4CA9IAU7RJ|GSK3532795|139 2312-45-6|1392312-45-6 (free base) |GSK-3532795|CHEMBL3827379|SCHEMBL1269786 2|BMS-955176 TFA|EX-A3677|BDBM50450015|BMS955176|DB15193 |2097784-79-5|AC-36687|HY-112714|CS-0062829|4 ( (1R, 3aS, 5aR, 5bR, 7aR, 11aS, 11bR, 13aR, 13bR) 3a- ( (2- (1, 1-Dioxidothiomorpholino) ethyl ) amino )-5a, 5b, 8, 8, 11a-penta methyl -1- (prop-1-en-2-yl ) -2, 3, 3a, 4, 5, 5a, 5b, 6, 7, 7a, 8, 11, 11a, 11b, 12, 13, 13a, 13boctad eca hydro1Hcyclopenta [a] chrysen-9-yl ) benzoic Acid|4-((1R, 3aS, 5aR, 5bR, 7aR, 11aS, 11bR, 13aR, 13bR)-3a-((2-(1, 1-dioxido-4-thiomorpholinyl)ethyl)amino)-1-isopropenyl-5a, 5b, 8, 8, 11a-pentamethyl-2, 3, 3a, 4, 5, 5a, 5b, 6, 7, 7a, 8, 11, 11a, 11b, 12, 13, 13a, 13b-octadecahydro-1H-cyclopenta[a]chrysen-9-yl)benzoic acid|4-((1R, 3aS, 5aR, 5bR, 7aR, 11aS, 11bR, 13aR, 13bR)-3a-((2-(1, 1-dioxidothiomorpholino)ethyl)amino)-5a, 5b, 8, 8, 11a-pentamethyl-1-(prop-1-en-2-yl)-2, 3, 3a, 4, 5, 5a, 5b, 6, 7, 7a, 8, 11, 11a, 11b, 12, 13, 13a, 13b-octadecahydro-1H-cyclopenta[a]chrysen-9-yl)benzoic acid|4-[(1R, 3aS, 5aR, 5bR, 7aR, 11aS, 11bR, 13aR, 13bR)-3a-[[2-(1, 1-dioxido-4-thiomorpholinyl)ethyl]amino]-2, 3, 3a, 4, 5, 5a, 5b, 6, 7, 7a, 8, 11, 11a, 11b, 12, 13, 13a, 13b-octadecahydro-5a, 5b, 8, 8, 11a-pentamethyl-1-(1-methylethenyl)-1H-cyclopenta[a]chrysen-9-yl]-benzoic acid|4-[(1R, 3aS, 5aR, 5bR. .. Grades: ≥98% (HPLC). CAS No. 1392312-45-6. Molecular formula: C42H62N2O4S. Mole weight: 691. |  |
| BMS-955176 free base | GSK3532795, also known as BMS-955176, is a potent, orally active, second-generation HIV-1 maturation inhibitor (MI) that advanced through phase IIb clinical trials. GSK3532795 combines broad coverage of polymorphic viruses (EC50 <15 nM toward a panel of common polymorphisms representative of 96.5% HIV-1 subtype B virus) with a favorable pharmacokinetic profile in preclinical species. Uses: Designed for use in research and industrial production. Additional or Alternative Names: GSK3532795; GSK-3532795; GSK 3532795; BMS-955176; BMS 955176; BMS955176. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 1392312-45-6. Molecular formula: C42H62N2O4S. Mole weight: 691.03. Purity:>98%. IUPACName: 4 - ((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR) - 3a-((2-(1,1-Dioxidothiomorpholino)ethyl)amino)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13boctadecahydro - 1H - cyclopenta[a]chrysen-9-yl)benzoic Acid. Canonical SMILES: O=C(O)C1=CC=C(C2=CC[C@@]3(C)[C@@](C2(C)C)([H])CC[C@@]4(C)[C@]5(C)CC[C@](CC[C@H]6C(C)=C)(NCCN(CC7)CCS7(=O)=O)[C@@]6([H])[C@@]5([H])CC[C@]34[H])C=C1. Product ID: ACM1392312456. Alfa Chemistry ISO 9001:2015 Certified. |  |
| BMS-955176 TFA | BMS-955176 TFA is the second generation HIV-1 maturation inhibitor. Synonyms: MS-955176 TFA. CAS No. 2097784-79-5. Molecular formula: C44H63F3N2O6S. Mole weight: 805.05. | |
| 4-methoxycarbonylphenylboronic acid | 4-(Methoxycarbonyl)phenylboronic Acid is used in the synthesis and evaluation of several organic compounds including that of 4-Cyclohexylbutyl-N-[(S)-2-oxoazetidin-3-yl]carbamate which is a potent inhibitor of intracellular NAAA activity. Also used in the design and synthesis of BMS-955176 which is a potent, orally active second generation HIV-1 maturation inhibitor. Synonyms: Methyl 4-boronobenzoate; (4-Carbomethoxyphenyl)boronic Acid; 4-Carbomethoxybenzeneboronic Acid; 4-Methoxycarbonylbenzeneboronic Acid; Methyl p-Boronobenzoate; p-(Methoxycarbonyl)boronic Acid; p-(Methoxycarbonyl)phenylboronic Acid; Benzoic acid, 4-borono-, 1-methyl ester; DTXSID40370259; Methyl 4-(dihydroxyboryl)benzoate; BP-11412; BR-45488; CC-19763. Grades: > 98 % (HPLC). CAS No. 99768-12-4. Molecular formula: C8H9BO4. Mole weight: 179.97. | |
| GSK3532795 | GSK3532795 (BMS-955176) is a potent, orally active, second-generation HIV-1 maturation inhibitor, with EC 50 s of 1.9, 10.2, 2.7 and 13 nM for HIV-1 WT, HIV-1 WT(human serum), HIV-1 V370A, and HIV-1 ΔV370, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMS-955176. CAS No. 1392312-45-6. Pack Sizes: 1 mg. Product ID: HY-112714. |  |
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