[EN] HETEROCYCLIC CARBOXYLIC ACID AMIDES AS PDK1 INIHIBITORS<br/>[FR] AMIDES D'ACIDE CARBOXYLIQUE HÉTÉROCYCLIQUES COMME INHIBITEURS DE PDK1
申请人:BOEHRINGER INGELHEIM INT
公开号:WO2011131741A1
公开(公告)日:2011-10-27
The present invention encompasses compounds of general formula (1) wherein the groups R1 to R4, Qa, Qb, QH, L and n are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations which contain such compounds and their use as medicaments.
The present invention encompasses compounds of general formula (1)
wherein the groups R
1
to R
4
, Q
a
, Q
b
, Q
H
, L and n are defined as in claim
1
, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations which contain such compounds and their use as medicaments.
Structure–property studies of an imidazoquinoline chemotype with antitrypanosomal activity
作者:Dana M. Klug、Rosario Diaz-Gonzalez、Travis J. DeLano、Eftychia M. Mavrogiannaki、Melissa J. Buskes、Raeann M. Dalton、John K. Fisher、Katherine M. Schneider、Vivian Hilborne、Melanie G. Fritsche、Quillon J. Simpson、Westley F. Tear、William G. Devine、Guiomar Pérez-Moreno、Gloria Ceballos-Pérez、Raquel García-Hernández、Cristina Bosch-Navarrete、Luis Miguel Ruiz-Pérez、Francisco Gamarro、Dolores González-Pacanowska、Maria Santos Martinez-Martinez、Pilar Manzano-Chinchon、Miguel Navarro、Michael P. Pollastri、Lori Ferrins
DOI:10.1039/d0md00103a
日期:——
Structure–property and structure–activity studies identify regions that positively modulate aqueous solubility; though maintaining potent anti-trypanosomal potency proves challenging.
结构-性质和结构-活性研究确定了能够正面调节水溶性的区域;尽管保持有效的抗锥虫活性证明具有挑战性。
1H-imidazo[4,5-c]quinolines
申请人:McConnell Darryl
公开号:US08895581B2
公开(公告)日:2014-11-25
The present invention encompasses compounds of general formula (1), wherein the groups R1 to R7, Qa, Qb, L, n and m are defined as in claim 1, which are suitable for the treatment of diseases characterized by excessive or abnormal cell proliferation, pharmaceutical preparations containing such compounds and their use as medicaments.
The present invention encompasses compounds of general formula (1), wherein the groups R
1
to R
7
, Q
a
, Q
b
, L, n and m are defined as in claim
1
, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations containing such compounds and their use as medicaments.