中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis and phosphodiesterase 5 inhibitory activity of novel pyrido[1,2-e]purin-4(3h)-one derivatives

文献类型:期刊论文

作者Xia, GX; Li, JF; Peng, AM; Lai, SN; Zhang, SJ; Shen, JS; Liu, ZH; Chen, XJ; Ji, RY
刊名Bioorganic & medicinal chemistry letters
出版日期2005-06-02
卷号15期号:11页码:2790-2794
关键词Pyrido[1,2-e]purin-4(3h)-one Pde5 inhibitor Sildenafil Erectile dysfunction
ISSN号0960-894X
DOI10.1016/j.bmcl.2005.03.102
通讯作者Shen, js()
英文摘要Synthesis and primary sar of a novel series of 2-phenylpyrido[1,2-e]purin-4(3h)-one derivatives with piperazinyl sulfonamide substituents were described herein. as potential pde5 inhibitors for erectile dysfunction (ed) treatment, representative compounds exhibit improved selectivity versus pde1 and pde6. meanwhile, compound 3e demonstrated functional efficacy on rabbit corpus cavernosum strip in vitro. (c) 2005 elsevier ltd. all rights reserved.
WOS关键词MALE ERECTILE DYSFUNCTION ; CYCLIC-NUCLEOTIDE PHOSPHODIESTERASES ; SELECTIVE PDE5 INHIBITORS ; POTENT ; SILDENAFIL ; CAVERNOSUM ; ANALOGS ; RELAXATION ; EXPRESSION ; ISOFORMS
WOS研究方向Pharmacology & Pharmacy ; Chemistry
WOS类目Chemistry, Medicinal ; Chemistry, Organic
语种英语
WOS记录号WOS:000229665600019
出版者PERGAMON-ELSEVIER SCIENCE LTD
URI标识http://www.irgrid.ac.cn/handle/1471x/2377415
专题中国科学院大学
通讯作者Shen, JS
作者单位1.Chinese Acad Sci, SIBS, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
2.Topharman Shanghai Co Ltd, Shanghai 201209, Peoples R China
3.Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
推荐引用方式
GB/T 7714
Xia, GX,Li, JF,Peng, AM,et al. Synthesis and phosphodiesterase 5 inhibitory activity of novel pyrido[1,2-e]purin-4(3h)-one derivatives[J]. Bioorganic & medicinal chemistry letters,2005,15(11):2790-2794.
APA Xia, GX.,Li, JF.,Peng, AM.,Lai, SN.,Zhang, SJ.,...&Ji, RY.(2005).Synthesis and phosphodiesterase 5 inhibitory activity of novel pyrido[1,2-e]purin-4(3h)-one derivatives.Bioorganic & medicinal chemistry letters,15(11),2790-2794.
MLA Xia, GX,et al."Synthesis and phosphodiesterase 5 inhibitory activity of novel pyrido[1,2-e]purin-4(3h)-one derivatives".Bioorganic & medicinal chemistry letters 15.11(2005):2790-2794.

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来源:中国科学院大学

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