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TitleStructure-based design of a new class of highly selective aminoimidazo[1,2-a]pyridine-based inhibitors of cyclin dependent kinases
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 15, Page 1943-1947, Year 2005
Publish dateJan 18, 2005 (structure data deposition date)
AuthorsHamdouchi, C. / Zhong, B. / Mendoza, J. / Collins, E. / Jaramillo, C. / De Diego, J.E. / Robertson, D. / Spencer, C.D. / Anderson, B.D. / Watkins, S.A. ...Hamdouchi, C. / Zhong, B. / Mendoza, J. / Collins, E. / Jaramillo, C. / De Diego, J.E. / Robertson, D. / Spencer, C.D. / Anderson, B.D. / Watkins, S.A. / Zhang, F. / Brooks, H.B.
External linksBioorg. Med. Chem. Lett. / PubMed:15780638
MethodsX-ray diffraction
Resolution1.8 Å
Structure data

PDB-1ykr:
Crystal structure of cdk2 with an aminoimidazo pyridine inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

Chemicals

ChemComp-628:
4-{[6-(2,6-DICHLOROBENZOYL)IMIDAZO[1,2-A]PYRIDIN-2-YL]AMINO}BENZENESULFONAMIDE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / cell cycle division protein kinase 2 / cdk2

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