882033-92-3Relevant articles and documents
Discovery of SARxxxx92, a pan-PIM kinase inhibitor, efficacious in a KG1 tumor model
Barberis, Claude,Erdman, Paul,Czekaj, Mark,Fire, Luke,Pribish, James,Tserlin, Elina,Maniar, Sachin,Batchelor, Joseph D.,Liu, Jinyu,Patel, Vinod F.,Hebert, Andrew,Levit, Mikhail,Wang, Anlai,Sun, Frank,Huang, Shih-Min A.
, (2020/11/20)
N-substituted azaindoles were discovered as potent pan-PIM inhibitors. Lead optimization, guided by structure and focused on physico-chemical properties allowed us to solve inherent hERG and permeability liabilities, and provided compound 27, which subseq
Synthesis and in vitro characterization of trans- and cis-[ 18F]-4-methylbenzyl 4-[(pyrimidin-2-ylamino)methyl]-3- fluoropiperidine-1-carboxylates as new potential PET radiotracer candidates for the NR2B subtype N-methyl-d-aspartate receptor
Koudih, Radouane,Gilbert, Gwenaelle,Dhilly, Martine,Abbas, Ahmed,Barre, Louisa,Debruyne, Daniele,Sobrio, Franck
experimental part, p. 408 - 415 (2012/08/13)
Diastereoisomeric compounds [18F]cis- and [18F]trans- 4-methylbenzyl 4-[(pyrimidin-2-ylamino)methyl]-3-fluoro-piperidine-1- carboxylates were successfully synthesized as new subtype-selective PET radiotracers for imaging the NR2B sub
Synthesis and SAR of substituted tetrahydrocarbazole derivatives as new NPY-1 antagonists
Di Fabio, Romano,Giovannini, Riccardo,Bertani, Barbara,Borriello, Manuela,Bozzoli, Andrea,Donati, Daniele,Falchi, Alessandro,Ghirlanda, Damiano,Leslie, Colin P.,Pecunioso, Angelo,Rumboldt, Giovanna,Spada, Simone
, p. 1749 - 1752 (2007/10/03)
The SAR of a new series of tetrahydrocarbazole derivatives is described: the appropriate decoration of this template led to the identification of a new class of NPY-1 antagonists showing good in vitro potency and a promising in vivo pharmacokinetic profil