阿舒瑞韋
外觀
阿舒瑞韋 | |
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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 | |
系統名 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 | |
別名 | BMS-650032 |
識別 | |
CAS號 | 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配體 | 10882 |
性質 | |
化學式 | C35H46ClN5O9S |
摩爾質量 | 748.29 g·mol−1 |
藥理學 | |
ATC代碼 | J05AP06(J05) |
藥品分級 | |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
阿舒瑞韋(INN:Asunaprevir;開發代號:BMS-650032),在日本和俄羅斯的商品名為Sunvepra,[2]是一種治療C型肝炎的實驗性候選藥物,由百時美施貴寶公司開發,已於2013年完成III期臨床試驗。[3]
阿舒瑞韋是C型肝炎病毒絲氨酸蛋白酶NS3的抑制劑。[4]阿舒瑞韋與聚乙二醇干擾素和利巴韋林的藥物組合正在進行測試,以及與其他直接作用抗病毒藥物(包括達拉他韋)在無干擾素方案中的聯合測試。[5][6][7]
參考資料
[編輯]- ^ Prescription medicines: registration of new chemical entities in Australia, 2015. Therapeutic Goods Administration (TGA). 21 June 2022 [10 April 2023]. (原始內容存檔於2023-04-10).
- ^ Sunvepra (asunaprevir) soft gelatin capsules 100 mg. Registration certificate. State Register of Medicines. [26 August 2015]. (原始內容存檔於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]. (原始內容存檔於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. (原始內容存檔於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]. (原始內容存檔於2014-01-18).
- ^ AASLD: Daclatasvir plus Asunaprevir Rapidly Suppresses HCV in Prior Null Responders 網際網路檔案館的存檔,存檔日期2015-02-08.. Highleyman, L. HIVandHepatitis.com. 8 November 2011.