中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
3-Arylamino-2H-1,2,4-benzothiadiazin-5-oI 1,1-dioxides as novel and selective CXCR2 antagonists

文献类型:期刊论文

作者Wang, Yonghui; Busch-Petersen, Jakob; Wang, Feng; Ma, Lanping; Fu, Wei; Kerns, Jeffrey K.; Jin, Jian; Palovich, Michael R.; Shen, Jing-Kang; Burman, Miriam
刊名BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
出版日期2007-07-15
卷号17期号:14页码:3864-3867
关键词CXCR2 antagonists interleukin-8 chemokines cyclic sulfonamides inflammation
ISSN号0960-894X
DOI10.1016/j.bmcl.2007.05.011
文献子类Article
英文摘要A series of 3-arylamino-2H-1,2,4-benzothiadiazin-5-oI 1,1-dioxides were prepared and shown to be novel and selective antagonists of the CXCR2 receptor. Synthesis, structure and activity relationships, selectivity, and some developability properties are described. (C) 2007 Elsevier Ltd. All rights reserved.
WOS关键词HUMAN INTERLEUKIN-8 RECEPTOR ; SMALL-MOLECULE ANTAGONISTS ; CHEMOKINE RECEPTOR ; NEUTROPHIL ; POTENT ; IDENTIFICATION ; EXPRESSION ; CLONING
WOS研究方向Pharmacology & Pharmacy ; Chemistry
语种英语
WOS记录号WOS:000248074600011
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://119.78.100.183/handle/2S10ELR8/273201]  
专题新药研究国家重点实验室
中科院受体结构与功能重点实验室
通讯作者Wang, Yonghui
作者单位1.GlaxoSmithKline Inc, Discovery Med Chem, Collegeville, PA 19426 USA
2.GlaxoSmithKline Inc, Resp & Immflamat CEDD, King Of Prussia, PA 19406 USA
3.Chinese Acad Sci, Inst Mat Med, State Key Lab Drug Res, Shanghai 20103, Peoples R China
推荐引用方式
GB/T 7714
Wang, Yonghui,Busch-Petersen, Jakob,Wang, Feng,et al. 3-Arylamino-2H-1,2,4-benzothiadiazin-5-oI 1,1-dioxides as novel and selective CXCR2 antagonists[J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,2007,17(14):3864-3867.
APA Wang, Yonghui.,Busch-Petersen, Jakob.,Wang, Feng.,Ma, Lanping.,Fu, Wei.,...&Widdowson, Katherine L..(2007).3-Arylamino-2H-1,2,4-benzothiadiazin-5-oI 1,1-dioxides as novel and selective CXCR2 antagonists.BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,17(14),3864-3867.
MLA Wang, Yonghui,et al."3-Arylamino-2H-1,2,4-benzothiadiazin-5-oI 1,1-dioxides as novel and selective CXCR2 antagonists".BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 17.14(2007):3864-3867.

入库方式: OAI收割

来源:上海药物研究所

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