化学
天然产物
小分子
羧肽酶
共晶
生物化学
凝血酶
合理设计
组合化学
立体化学
分子
酶
有机化学
纳米技术
血小板
氢键
材料科学
免疫学
生物
作者
Nis Halland,Mark Brönstrup,Jörg Czech,Werngard Czechtizky,Andreas Evers,Markus Follmann,Markus Kohlmann,Matthias Schiell,Michael Kurz,Herman Schreuder,Christopher Kallus
摘要
Anabaenopeptins isolated from cyanobacteria were identified as inhibitors of carboxypeptidase TAFIa. Cocrystal structures of these macrocyclic natural product inhibitors in a modified porcine carboxypeptidase B revealed their binding mode and provided the basis for the rational design of small molecule inhibitors with a previously unknown central urea motif. Optimization based on these design concepts allowed for a rapid evaluation of the SAR and delivered potent small molecule inhibitors of TAFIa with a promising overall profile.
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