Discovery of hydroxyl 1,2-diphenylethanamine analogs as potent cholesterol ester transfer protein inhibitors

[Display omitted] 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 (DP...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2016-07, Vol.26 (14), p.3278-3281
Hauptverfasser: Jiang, Ji, Finlay, Heather, Johnson, James A., Harikrishnan, Lalgudi, Kamau, Muthoni, Qiao, Jennifer, Wang, Tammy, Adam, Leonard, Taylor, David, Yang, Richard, Sleph, Paul, Chen, Alice Ye A., Yin, Xiaohong, Wexler, Ruth, Salvati, Mark E.
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Sprache:eng
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Zusammenfassung:[Display omitted] 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.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2016.05.058