Development of methyl isoxazoleazepines as inhibitors of BET.
Bioorg Med Chem Lett
; 25(9): 1842-8, 2015 May 01.
Article
in En
| MEDLINE
| ID: mdl-25851940
In this report we detail the evolution of our previously reported thiophene isoxazole BET inhibitor chemotype exemplified by CPI-3 to a novel bromodomain selective chemotype (the methyl isoxazoleazepine chemotype) exemplified by carboxamide 23. The methyl isoxazoleazepine chemotype provides potent inhibition of the bromodomains of the BET family, excellent in vivo PK across species, low unbound clearance, and target engagement in a MYC PK-PD model.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Oxazoles
/
Azepines
/
Transcription Factors
/
Nuclear Proteins
/
Drug Design
/
RNA-Binding Proteins
/
Protein Serine-Threonine Kinases
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Bioorg Med Chem Lett
Journal subject:
BIOQUIMICA
/
QUIMICA
Year:
2015
Type:
Article