四氢异喹啉
化学
雌激素受体
体内
生物利用度
药理学
药代动力学
乳腺癌
药物发现
癌症
癌症研究
立体化学
内科学
生物化学
医学
生物
生物技术
作者
Heather E. Burks,Tinya J. Abrams,C.A. Kirby,Jason R. Baird,Alexander Fekete,Lawrence G. Hamann,Sunkyu Kim,Franco Lombardo,Alice Loo,Danuta Lubicka,Kaitlin J. Macchi,Donald P. McDonnell,Yuji Mishina,John D. Norris,Jill Nunez,Chitra Saran,Yingchuan Sun,Noel M. Thomsen,Chunrong Wang,Li Wang,Stefan Peukert
标识
DOI:10.1021/acs.jmedchem.6b01468
摘要
Tetrahydroisoquinoline 40 has been identified as a potent ERα antagonist and selective estrogen receptor degrader (SERD), exhibiting good oral bioavailability, antitumor efficacy, and SERD activity in vivo. We outline the discovery and chemical optimization of the THIQ scaffold leading to THIQ 40 and showcase the racemization of the scaffold, pharmacokinetic studies in preclinical species, and the in vivo efficacy of THIQ 40 in a MCF-7 human breast cancer xenograft model.
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