CAS: 1233335-78-8; Sofosbuvir Metabolites Gs566500

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sofosbuvir

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  • 合成目标产物 Sofosbuvir Metabolites Gs566500 主要起始原料 Psi 7851
  • (文献来源)合成步骤主要原料 Psi 7851
📜索罗布维置于水,三乙胺体系中,化学反应 30.0H,以92%的收率获得索非布韦代谢物gs-566500
参考文献: Nucleoside Phosphoramidate Prodrugs[fr] Analogues De Nucléoside
标题: Nucleoside Phosphoramidate Prodrugs[fr] Analogues De Nucléoside

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主要参考文献


1: Custodio JM, Chuck SK, Chu H, Cao H, Ma G, Flaherty J, Ling J, Kearney BP. Lack of clinically important PK interaction between coformulated ledipasvir/sofosbuvir and rilpivirine/emtricitabine/tenofovir alafenamide. Pharmacol Res Perspect. 2017 Oct;5(5). doi: 10.1002/prp2.353.
2: Lawitz E, Rodriguez-Torres M, Denning JM, Albanis E, Cornpropst M, Berrey MM, Symonds WT. Pharmacokinetics, pharmacodynamics, and tolerability of GS-9851, a nucleotide analog polymerase inhibitor, following multiple ascending doses in patients with chronic hepatitis C infection. Antimicrob Agents Chemother. 2013 Mar;57(3):1209-17. doi: 10.1128/AAC.01263-12. Epub 2012 Dec 21.
3: Denning J, Cornpropst M, Flach SD, Berrey MM, Symonds WT. Pharmacokinetics, safety, and tolerability of GS-9851, a nucleotide analog polymerase inhibitor for hepatitis C virus, following single ascending doses in healthy subjects. Antimicrob Agents Chemother. 2013 Mar;57(3):1201-8. doi: 10.1128/AAC.01262-12. Epub 2012 Dec 21.
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