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1.
Discovery of vimseltinib (DCC-3014), a highly selective CSF1R switch-control kinase inhibitor, in clinical development for the treatment of Tenosynovial Giant Cell Tumor (TGCT).
Bioorg Med Chem Lett
; 74: 128928, 2022 10 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-35961460
2.
Discovery of acyl ureas as highly selective small molecule CSF1R kinase inhibitors.
Bioorg Med Chem Lett
; 74: 128929, 2022 10 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-35961461
3.
Vimseltinib: A Precision CSF1R Therapy for Tenosynovial Giant Cell Tumors and Diseases Promoted by Macrophages.
Mol Cancer Ther
; 20(11): 2098-2109, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34433663
4.
Ripretinib (DCC-2618) Is a Switch Control Kinase Inhibitor of a Broad Spectrum of Oncogenic and Drug-Resistant KIT and PDGFRA Variants.
Cancer Cell
; 35(5): 738-751.e9, 2019 05 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-31085175
5.
Altiratinib Inhibits Tumor Growth, Invasion, Angiogenesis, and Microenvironment-Mediated Drug Resistance via Balanced Inhibition of MET, TIE2, and VEGFR2.
Mol Cancer Ther
; 14(9): 2023-34, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-26285778
6.
Discovery of 1-(3,3-dimethylbutyl)-3-(2-fluoro-4-methyl-5-(7-methyl-2-(methylamino)pyrido[2,3-d]pyrimidin-6-yl)phenyl)urea (LY3009120) as a pan-RAF inhibitor with minimal paradoxical activation and activity against BRAF or RAS mutant tumor cells.
J Med Chem
; 58(10): 4165-79, 2015 May 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-25965804
7.
The rational synthesis of chlorins via rearrangement of porphodimethenes: influence of beta-substituents on the regioselectivity and stereoselectivity of pyrroline ring formation.
J Org Chem
; 67(13): 4536-46, 2002 Jun 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-12076154
8.
CRHR1 Receptor binding and lipophilicity of pyrrolopyrimidines, potential nonpeptide corticotropin-releasing hormone type 1 receptor antagonists.
Bioorg Med Chem
; 10(1): 175-83, 2002 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-11738619
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