MEDI 389-Discovery and structure-activity relationships of substituted tetrahydroisoquinoline as liver X receptor (LXR) agonists

被引：0

作者：

Yang, Wu ^{[1
]}

Wang, Yufeng ^{[1
]}

Nirschl, David ^{[2
]}

Duclos, Franck ^{[3
]}

Hsiang, Bonnie ^{[3
]}

Ryan, Carol ^{[3
]}

Scheer, Susan ^{[3
]}

Ostrowski, Jacek ^{[3
]}

Lupisella, John ^{[3
]}

Kuhns, Joyce ^{[3
]}

Morgan, Maureen ^{[3
]}

OMalley, Kevin ^{[4
]}

Lippy, Jonathan ^{[4
]}

Locke, Kenneth ^{[4
]}

Zhang, Litao ^{[4
]}

Lawrence, Michael ^{[1
]}

Poss, Michael ^{[1
]}

Blanar, Michael ^{[3
]}

Wexler, Ruth ^{[1
]}

Kirchgessner, Todd ^{[3
]}

Kick, Ellen ^{[1
]}

机构：

[1] Bristol Myers Squibb Co, Res & Dev, Discovery Chem, Princeton, NJ 08543 USA

[2] Bristol Myers Squibb Co, Res & Dev, SATT Synth, Princeton, NJ 08543 USA

[3] Bristol Myers Squibb Co, Res & Dev, Metab & Cardiovasc Drug Discovery, Princeton, NJ 08543 USA

[4] Bristol Myers Squibb Co, Res & Dev, Lead Evaluat, Princeton, NJ 08543 USA

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2008年 / 236卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

389-MEDI

引用

页数：1

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