![BMS-626529 Size:Solid 2 mg Smiles: OC1(CN(C1)C(=O)C1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F)[C@H]1CCCCN1](https://cdn.shopify.com/s/files/1/0389/1897/9723/products/M10076_1621561286.gif?v=1621561288)
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Smiles: OC1(CN(C1)C(=O)C1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F)[C@H]1CCCCN1
PMCID: PMC5469273
acetylcholine
InChiKey: VVIAGPKUTFNRDU-ABLWVSNPSA-N
InChi: InChI=1S/C20H13NO5/c22-20-12-5-10-2-4-15-19(26-9-24-15)18(10)17(13(12)7-21-20)11-1-3-14-16(6-11)25-8-23-14/h1-6H
BMS-626529 Size:Solid 2 mg Smiles: OC1(CN(C1)C(=O)C1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F)[C@H]1CCCCN1Temsavir, also known as BMS 626529, is a potent HIV 1 attachment inhibitor. BMS 663068 is also the phosphonooxymethyl prodrug of BMS 626529 that targets HIV 1 gp120 and prevents its binding to CD4(+) T cells. BMS 626529 had half maximal effective concentration (EC(50)) values of <10 nM against the vast majority of viral isolates; however, susceptibility varied by >6 log(10), with half maximal effective concentration values in the low pM range against
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