Synthesis, biological evaluation and molecular modelling of sulfonohydrazides as selective PI3K p110α inhibitors
摘要:
A series of 2-methyl-5-nitrobenzenesulfonohydrazides were prepared and evaluated as inhibitors of PI3K. An isoquinoline derivative shows good selectivity for the p110 alpha isoform over p110 beta and p110 delta, and also demonstrates good in vitro activity in a cell proliferation assay. Molecular modelling provides a rationalisation for the observed SAR. (c) 2007 Elsevier Ltd. All rights reserved.
Disclosed are compounds, compositions and methods for treating of diseases, syndromes, conditions, and disorders that are affected by the modulation of MALT1. Such compounds are represented by Formula (I) as follows:
wherein R1, R2, R3, R4, R5, R6, R5, G1, and G2 are defined herein.
[EN] PYRAZOLE DERIVATIVES AS MALT1 INHIBITORS<br/>[FR] DÉRIVÉS DE PYRAZOLE EN TANT QU'INHIBITEURS DE MALT1
申请人:JANSSEN BIOTECH INC
公开号:WO2018119036A1
公开(公告)日:2018-06-28
Disclosed are compounds, compositions and methods for treating of diseases, syndromes, conditions, and disorders that are affected by the modulation of MALT1. Such compounds are represented by Formula (I) wherein R1, R2, R3, R4, R5, R6, R5, G1, and G2 are defined herein.