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Bioorg Med Chem Lett ; 19(19): 5576-81, 2009 Oct 01.
Article in English | MEDLINE | ID: mdl-19716296

ABSTRACT

SAR for a wide variety of heterocyclic replacements for a benzimidazole led to the discovery of functionalized 2-pyridyl amides as novel inhibitors of the hedgehog pathway. The 2-pyridyl amides were optimized for potency, PK, and drug-like properties by modifications to the amide portion of the molecule resulting in 31 (GDC-0449). Amide 31 produced complete tumor regression at doses as low as 12.5mg/kg BID in a medulloblastoma allograft mouse model that is wholly dependent on the Hh pathway for growth and is currently in human clinical trials, where it is initially being evaluated for the treatment of BCC.


Subject(s)
Amides/chemistry , Anilides/chemistry , Hedgehog Proteins/metabolism , Pyridines/chemistry , Amides/chemical synthesis , Amides/pharmacology , Anilides/chemical synthesis , Anilides/pharmacology , Animals , Benzimidazoles/chemistry , Carcinoma, Basal Cell/drug therapy , Cell Line , Cerebellar Neoplasms/drug therapy , Hedgehog Proteins/antagonists & inhibitors , Humans , Medulloblastoma/drug therapy , Mice , Mice, Nude , Pyridines/chemical synthesis , Pyridines/pharmacology , Signal Transduction , Structure-Activity Relationship , Xenograft Model Antitumor Assays
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