盐酸帕洛诺司琼合成路线图解
被引量:4
Graphical Synthetic Routes of Palonosetron Hydrochloride
摘要
帕洛诺司琼(Palonosetron,1),化学名为(3aS)-2-[(3S)-1-氮杂二环[2.2.2]辛烷.3.基]-2,3,3a,4,5,6-六氢-1-氧代-1H-苯并[de]异喹啉,是由瑞士Helsinn公司研制的5.HT,受体拮抗剂,其盐酸盐于2003年7月首次在美国上市,商品名Aloxi(阿乐喜),临床用于预防中度或高度致吐性化疗引发的急性和迟发性恶心呕吐。本品半衰期长(40h),
出处
《中国医药工业杂志》
CAS
CSCD
北大核心
2009年第3期231-233,共3页
Chinese Journal of Pharmaceuticals
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共引文献28
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同被引文献18
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引证文献4
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1朱阳,龚玲,杨立平,孙恺.盐酸帕洛诺司琼的合成[J].中国医药工业杂志,2009,40(4):241-243.
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2王嘉林,王斯坦.HP-β-CD手性添加剂反相高效液相色谱拆分盐酸帕洛诺司琼S,R异构体[J].中国药师,2015,18(2):237-240. 被引量:6
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3曹天海.GC测定盐酸帕洛诺司琼原料药中(S)-3-氨基-奎宁的含量[J].中国执业药师,2016,13(3):27-29.
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