Structure-based design and SAR development of 5,6-dihydroimidazolo[1,5-f]pteridine derivatives as novel Polo-like kinase-1 inhibitors.
Bioorg Med Chem Lett
; 27(5): 1311-1315, 2017 03 01.
Article
in En
| MEDLINE
| ID: mdl-28169164
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Pteridines
/
Drug Design
/
Proto-Oncogene Proteins
/
Protein Serine-Threonine Kinases
/
Cell Cycle Proteins
/
Imidazoles
Limits:
Animals
/
Female
/
Humans
Language:
En
Journal:
Bioorg Med Chem Lett
Journal subject:
BIOQUIMICA
/
QUIMICA
Year:
2017
Document type:
Article
Country of publication:
United kingdom