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1.
Design and synthesis of aminopyridine containing biaryls reducing c-MYC protein levels in cells.
Bioorg Med Chem Lett
; 92: 129385, 2023 08 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-37339719
2.
Cell-Based Drug Discovery: Identification and Optimization of Small Molecules that Reduce c-MYC Protein Levels in Cells.
J Med Chem
; 64(21): 16056-16087, 2021 11 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34669409
3.
Biochemical characterization of GSK1070916, a potent and selective inhibitor of Aurora B and Aurora C kinases with an extremely long residence time1.
Biochem J
; 420(2): 259-65, 2009 May 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-19284385
4.
Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinases.
Bioorg Med Chem Lett
; 17(1): 250-4, 2007 Jan 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-17027260
5.
Orally active 4-amino-5-diarylurea-furo[2,3-d]pyrimidine derivatives as anti-angiogenic agent inhibiting VEGFR2 and Tie-2.
Bioorg Med Chem Lett
; 17(6): 1773-8, 2007 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-17276055
6.
Discovery of a novel and potent series of dianilinopyrimidineurea and urea isostere inhibitors of VEGFR2 tyrosine kinase.
Bioorg Med Chem Lett
; 15(15): 3519-23, 2005 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-15990302
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