Discovery of orally available tetrahydroquinoline-based glucocorticoid receptor agonists
摘要:
A series of tetrahydroquinoline derivatives were synthesized and profiled for their ability to act as glucocorticoid receptor selective modulators. Structure-activity relationships of the tetrahydroquinoline B-ring lead to the discovery of orally available GR-selective agonists with high in vivo activity. (C) 2011 Elsevier Ltd. All rights reserved.
Novel substituted decahydroquinolines are prepared and used as ultraviolet (UV) light stabilizers for materials subject to UV light degradation, particularly for polyolefins. Compositions containing the decahydroquinoline compounds exhibit excellent stability to UV light.
An efficient process has been developed for the synthesis of 2,2,4-trisubstituted-1,2-dihydroquinolines in good yields through a simple one-pot condensation between anilines and ketones in the presence of zinctriflate as a catalyst at room temperature undersolvent-freeconditions.
Mild and Convenient Synthesis of 1,2‐Dihydroquinolines from Anilines and Acetone Catalyzed by Ytterbium(III) Triflate in Ionic Liquids
作者:Yongshu Li、Chunlei Wu、Jianliang Huang、Weike Su
DOI:10.1080/00397910600775374
日期:2006.10
Abstract A mild, convenient, and efficient process has been developed for the synthesis of 2,2,4‐trimethyl‐1,2‐dihydroquinolines by the reaction of anilines with acetone catalyzed by ytterbium(III) triflate [Yb(OTf)3] in ionicliquids. The catalyst and ionicliquids can be easily recovered and reused, making this method friendly and environmentally acceptable.
Substituted decahydroquinolines and their use as ultraviolet light
申请人:The B. F. Goodrich Company
公开号:US04073770A1
公开(公告)日:1978-02-14
Novel substituted decahydroquinolines are prepared and used as ultraviolet (UV) light stabilizers for materials subject to UV light degradation, particularly for polyolefins. Compositions containing the decahydroquinoline compounds exhibit excellent stability to UV light.
Stimulation of natural killer cells with small molecule inhibitors of CD38 for the treatment of neuroblastoma
作者:Catherine M. Mills、Thomas Z. Benton、Ivett Piña、Megan J. Francis、Leticia Reyes、Nathan G. Dolloff、Yuri K. Peterson、Patrick M. Woster
DOI:10.1039/d2sc05749b
日期:——
Small molecule inhibitors of CD38 promote increases in interferon gamma and stimulate natural killer cell proliferation for the treatment of neuroblastoma.