Agonist lead identification for the high affinity niacin receptor GPR109a
摘要:
A strategy for lead identification of new agonists of GPR109a, starting from known compounds shown to activate the receptor, is described. Early compound triage led to the formulation of a binding hypothesis and eventually to our focus on a series of pyrazole acid derivatives. Further elaboration of these compounds provided a series of 5,5-fused pyrazoles to be used as lead compounds for further optimization. (C) 2007 Elsevier Ltd. All rights reserved.
Mugnaini; Gruenanger, Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti, <hi>1953</hi>, vol. <8>14, p. 95,97,275,277
作者:Mugnaini、Gruenanger
DOI:——
日期:——
WO2024098066A1
申请人:——
公开号:——
公开(公告)日:——
[EN] EXATECAN DERIVATIVES AND ANTIBODY-DRUG CONJUGATES THEREOF<br/>[FR] DÉRIVÉS D'EXATECAN ET CONJUGUÉS ANTICORPS-MÉDICAMENT DE CEUX-CI
申请人:[en]ALX ONCOLOGY INC.
公开号:WO2022236136A1
公开(公告)日:2022-11-10
Disclosed herein, in part, are compounds (I) which are exatecan derivatives with novel chemical linkers that include cathepsin B cleavable moieties, and conjugated to targeting antibodies.