Optimization of TEAD P-Site Binding Fragment Hit into In Vivo Active Lead <b>MSC-4106</b>
作者:Timo Heinrich、Carl Peterson、Richard Schneider、Sakshi Garg、Daniel Schwarz、Jakub Gunera、Anita Seshire、Lisa Kötzner、Sarah Schlesiger、Djordje Musil、Heike Schilke、Benjamin Doerfel、Patrizia Diehl、Pia Böpple、Ana R. Lemos、Pedro M. F. Sousa、Filipe Freire、Tiago M. Bandeiras、Emma Carswell、Nicholas Pearson、Sameer Sirohi、Mollie Hooker、Elisabeth Trivier、Rebecca Broome、Alexander Balsiger、Abigail Crowden、Christian Dillon、Dirk Wienke
DOI:10.1021/acs.jmedchem.2c00403
日期:2022.7.14
[EN] HETEROBIFUNCTIONAL MOLECULES AS TEAD INHIBITORS<br/>[FR] MOLÉCULES HÉTÉROBIFONCTIONNELS UTILISÉES EN TANT QU'INHIBITEURS DE TEAD
申请人:[en]MERCK PATENT GMBH
公开号:WO2023078813A1
公开(公告)日:2023-05-11
Compounds of the formula (I) Q1-Q2-Q3(I) in which Q1, Q2and Q3have the meanings indicated in Claim 1, degrade target proteins, and can be employed, inter alia, for the treatment of diseases and conditions mediated by such target proteins.