阿舒瑞韦
外观
阿舒瑞韦 | |
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IUPAC名 3-Methyl-N[(2-methyl-2-propanyl)oxy]carbonylL-valyl-(4R)-4-[(7-chloro-4-methoxy-1-isoquinolinyl)oxy]-N(1R,2S)-1-[(cyclopropylsulfonyl)carbamoyl]-2-vinylcyclopropylL-prolinamide | |
系统名 tert-Butyl {(2S)-1-[(32S,34R,61R,62S)-17-chloro-62-ethenyl-14-methoxy-4,7,9,9-tetraoxo-2-oxa-9λ6-thia-5,8-diaza-1(1)-isoquinolina-3(4,2)-pyrrolidina-6(1,1),10(1)-dicyclopropadecaphan-31-yl]-3,3-dimethyl-1-oxobutan-2-yl}carbamate | |
别名 | BMS-650032 |
识别 | |
CAS号 | 630420-16-5 |
PubChem | 16076883 |
ChemSpider | 17235944 |
SMILES |
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InChI |
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InChIKey | XRWSZZJLZRKHHD-WVWIJVSJBJ |
ChEBI | 134723 |
DrugBank | DB11586 |
KEGG | D10093 |
IUPHAR配体 | 10882 |
性质 | |
化学式 | C35H46ClN5O9S |
摩尔质量 | 748.29 g·mol−1 |
药理学 | |
ATC代码 | J05AP06(J05) |
药品分级 | |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
阿舒瑞韦(INN:Asunaprevir;开发代号:BMS-650032),在日本和俄罗斯的商品名为Sunvepra,[2]是一种治疗丙型肝炎的实验性候选药物,由百时美施贵宝公司开发,已于2013年完成III期临床试验。[3]
阿舒瑞韦是丙型肝炎病毒丝氨酸蛋白酶NS3的抑制剂。[4]阿舒瑞韦与聚乙二醇干扰素和利巴韦林的药物组合正在进行测试,以及与其他直接作用抗病毒药物(包括达拉他韦)在无干扰素方案中的联合测试。[5][6][7]
参考资料
[编辑]- ^ Prescription medicines: registration of new chemical entities in Australia, 2015. Therapeutic Goods Administration (TGA). 21 June 2022 [10 April 2023]. (原始内容存档于2023-04-10).
- ^ Sunvepra (asunaprevir) soft gelatin capsules 100 mg. Registration certificate. State Register of Medicines. [26 August 2015]. (原始内容存档于2016-03-04) (Russian).
- ^ A Phase 3 Study in Combination With BMS-790052 and BMS-650032 in Japanese Hepatitis C Virus (HCV) Patients. ClinicalTrials.gov. 23 September 2015 [2024-03-03]. (原始内容存档于2014-07-14).
- ^ C. Reviriego. Asunaprevir. HCV serine protein NS3 inhibitor, Treatment of hepatitis C virus. Drugs of the Future. 2012, 37 (4): 247–254 [2024-03-03]. doi:10.1358/dof.2012.037.04.1789350. (原始内容存档于2018-06-03).
- ^ Lok AS, Gardiner DF, Lawitz E, Martorell C, Everson GT, Ghalib R, Reindollar R, Rustgi V, McPhee F, Wind-Rotolo M, Persson A, Zhu K, Dimitrova DI, Eley T, Guo T, Grasela DM, Pasquinelli C. Preliminary study of two antiviral agents for hepatitis C genotype 1. The New England Journal of Medicine. January 2012, 366 (3): 216–24. PMID 22256805. doi:10.1056/NEJMoa1104430 .
- ^ Bristol-Myers' Daclatasvir, Asunaprevir Cured 77%: Study. Bloomberg. Apr 19, 2012 [2024-03-03]. (原始内容存档于2014-01-18).
- ^ AASLD: Daclatasvir plus Asunaprevir Rapidly Suppresses HCV in Prior Null Responders 互联网档案馆的存檔,存档日期2015-02-08.. Highleyman, L. HIVandHepatitis.com. 8 November 2011.