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Simeprevir的合成路线图解 被引量:1

Graphical Synthetic Routes of Simeprevir
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摘要 Simeprevir(TMC-435,1),化学名为(2R,3aR,10Z,11aS,12aR,14aR)-N-(环丙磺酰基)-2,3,3a,4,5,6,7,8,9,11a,12,13,14,14a-十四氢-2-[[7-甲氧基-8-甲基-2-[4-(1-甲基乙基)-2-噻唑基]-4-喹啉基]-氧基]-5-甲基-4,14-二氧代环戊并[c]环丙并[g][1,6]-二氮杂环十四烯-12a(1H)-甲酰胺,是由Medivir公司和Janssen联合开发的新一代NS3/4A蛋白酶抑制剂,2013年首次在加拿大、日本和美国上市,临床用于治疗慢性丙型肝炎。
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2014年第9期891-895,共5页 Chinese Journal of Pharmaceuticals
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参考文献14

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共引文献7

同被引文献13

  • 1Parsy CC, Alexandre F, Convard T, et al. Macrocyclic serine protease inhibitors, pharmaceutical compositions thereof, and their use for treating HCV infections: WO, 2012109398 [P]. 2012-08-16.
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  • 5朱坡,杨细纹,王忠良,等.一种HCV蛋白酶抑制剂重要中间体的制备方法:中国,102531932[P].2012-07-04.
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  • 10Buckman B, Serebryany V, Nicholas JB, et al. Novel macrocyclic inbibitors of hepatitis C virus replication: WO, 2012054874 [P]. 2012-04-26.

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