化学
免疫
海湾
癌症
细胞免疫
免疫系统
免疫学
内科学
医学
生物
土木工程
工程类
作者
Jeffrey Mowat,Rafael Carretero,Gabriele Leder,Núria Aiguabella Font,Roland Neuhaus,Sandra Berndt,Judith Günther,Anders Friberg,Martina Schäfer,Hans Briem,Marian Raschke,Hideki Miyatake Ondozabal,Bernd Buchmann,Ulf Boemer,Bertolt Kreft,Ingo V. Hartung,Rienk Offringa
标识
DOI:10.1021/acs.jmedchem.4c01325
摘要
Mitogen-activated protein kinase kinase kinase kinase 1 (MAP4K1) is a serine/threonine kinase that acts as an immune checkpoint downstream of T-cell receptor stimulation. MAP4K1 activity is enhanced by prostaglandin E2 (PGE2) and transforming growth factor beta (TGFβ), immune modulators commonly present in the tumor microenvironment. Therefore, its pharmacological inhibition is an attractive immuno-oncology concept for inducing therapeutic T-cell responses in cancer patients. Here, we describe the systematic optimization of azaindole-based lead compound
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