Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1368689 | Bioorganic & Medicinal Chemistry Letters | 2016 | 4 Pages |
Abstract
Hydroxyl 1,2-diphenylethanamine analogs were identified as potent inhibitors of cholesterol ester transfer protein (CETP), a therapeutic target to raise HDL cholesterol. In an effort to improve the pharmaceutical properties in the previously disclosed DiPhenylPyridineEthanamine (DPPE) series, polar groups were introduced to the N-linked quaternary center. Optimization of analogues for potency, in vitro liability profile and efficacy led to identification of lead compound 16 which demonstrated robust pharmacodynamic effects in human CETP/apo-B100 dual transgenic mice.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ji Jiang, Heather Finlay, James A. Johnson, Lalgudi Harikrishnan, Muthoni Kamau, Jennifer Qiao, Tammy Wang, Leonard Adam, David Taylor, Richard Yang, Paul Sleph, Alice Ye A. Chen, Xiaohong Yin, Ruth Wexler, Mark E. Salvati,