Literature summary for 2.7.11.22 extracted from

De Azevedo, W.F., Jr.; Mueller-Dieckmann, H.J.; Schulze-Gahmen, U.; Worland, P.J.; Sausville, E.; Kim, S.H.
Structural basis for specificity and potency of a flavonoid inhibitor of human CDK2, a cell cycle kinase (1996), Proc. Natl. Acad. Sci. USA, 93, 2735-2740.

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Crystallization (Commentary)

Crystallization (Comment)	Organism
crystal structure of a complex between CDK2 and (-)-cis-5,7-dihydroxyphenyl-8-[4-(3-hydroxy-1-methyl)piperidinyl] -4H-1-benzopyran-4-one hydrochloride hemihydrate, L868276	Homo sapiens

Inhibitors

Inhibitors	Comment	Organism	Structure
(-)-cis-5,7-dihydroxyphenyl-8-[4-(3-hydroxy-1-methyl)piperidinyl]-4H-1-benzopyran-4-one	-	Homo sapiens

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	P24941	-	-

Synonyms

Synonyms	Comment	Organism
cell division protein kinase 2	-	Homo sapiens

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Release 2023.1 (January 2023)