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公开(公告)号:WO2012141487A2
公开(公告)日:2012-10-18
申请号:PCT/KR2012/002739
申请日:2012-04-12
申请人: CHONG KUN DANG PHARMACEUTICAL CORP. , LEE, Seohee , OH, Jungtaek , LEE, Jaekwang , LEE, Jaewon , BAE, Suyeal , HA, Nina , LEE, Sera
发明人: LEE, Seohee , OH, Jungtaek , LEE, Jaekwang , LEE, Jaewon , BAE, Suyeal , HA, Nina , LEE, Sera
IPC分类号: C07D263/16 , C07D263/22 , C07D413/06 , A61K31/421 , A61P9/00 , A61P3/06
CPC分类号: C07D263/24 , C07D263/16 , C07D263/22 , C07D401/06 , C07D413/06 , C07D413/08 , C07D413/10 , C07D417/12
摘要: The present invention relates to cycloalkenyl aryl derivatives, isomers thereof, pharmaceutically acceptable salts thereof, hydrates thereof, or solvates thereof; a method for preparing the derivatives; and pharmaceutical compositions containing the same. The compounds of the present invention show the effect of CETP activity inhibition. It means that the compounds can increase HDL-cholesterol and decrease LDL-cholesterol.
摘要翻译: 本发明涉及环烯基芳基衍生物,其异构体,其药学上可接受的盐,其水合物或溶剂合物; 制备衍生物的方法; 和含有它们的药物组合物。 本发明的化合物显示CETP活性抑制的作用。 这意味着这些化合物可以增加HDL-胆固醇并降低LDL-胆固醇。
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公开(公告)号:WO2012141487A3
公开(公告)日:2013-01-10
申请号:PCT/KR2012002739
申请日:2012-04-12
申请人: CHONG KUN DANG PHARM CORP , LEE SEOHEE , OH JUNGTAEK , LEE JAEKWANG , LEE JAEWON , BAE SUYEAL , HA NINA , LEE SERA
发明人: LEE SEOHEE , OH JUNGTAEK , LEE JAEKWANG , LEE JAEWON , BAE SUYEAL , HA NINA , LEE SERA
IPC分类号: C07D263/16 , A61K31/421 , A61P3/06 , A61P9/00 , C07D263/22 , C07D413/06
CPC分类号: C07D263/24 , C07D263/16 , C07D263/22 , C07D401/06 , C07D413/06 , C07D413/08 , C07D413/10 , C07D417/12
摘要: The present invention relates to cycloalkenyl aryl derivatives, isomers thereof, pharmaceutically acceptable salts thereof, hydrates thereof, or solvates thereof; a method for preparing the derivatives; and pharmaceutical compositions containing the same. The compounds of the present invention show the effect of CETP activity inhibition. It means that the compounds can increase HDL-cholesterol and decrease LDL-cholesterol.
摘要翻译: 本发明涉及环烯基芳基衍生物,其异构体,其药学上可接受的盐,其水合物或溶剂合物; 制备衍生物的方法; 和含有它们的药物组合物。 本发明的化合物显示CETP活性抑制的作用。 这意味着这些化合物可以增加HDL-胆固醇并降低LDL-胆固醇。
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