SCOPUS 정보 검색 플랫폼

Nucleosides, Nucleotides and Nucleic Acids

Volumn 20, Issue 4-7, 2001, Pages 1067-1078

The design and synthesis of purine inhibitors of CDK2. III

(16) Shum, P W a Peet, N P a Weintraub, P M a Le, T B a Zhao, Z a Barbone, F a Cashman, B a Tsay, J a Dwyer, S a Loos, P C a Powers, E A a Kropp, K a Wright, P S a Bitonti, A a Dumont, J a Borcherding, D R a

a SANOFI (France)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN DEPENDENT KINASE 2; CYCLIN DEPENDENT KINASE INHIBITOR; CYCLIN E; PURINE ANTAGONIST;

ANTINEOPLASTIC ACTIVITY; BINDING AFFINITY; CELL CYCLE G1 PHASE; CELL CYCLE S PHASE; CELL DIVISION; CELL GROWTH; CONFERENCE PAPER; REGULATORY MECHANISM; STRUCTURE ACTIVITY RELATION;

ADENINE; ANIMALS; ANTINEOPLASTIC AGENTS; CDC2-CDC28 KINASES; CYCLIN-DEPENDENT KINASE 2; CYCLIN-DEPENDENT KINASES; DRUG DESIGN; DRUG SCREENING ASSAYS, ANTITUMOR; ENZYME INHIBITORS; HT29 CELLS; HUMANS; MICE; MICE, NUDE; PIPERIDINES; PROTEIN-SERINE-THREONINE KINASES; PURINES; STRUCTURE-ACTIVITY RELATIONSHIP; TUMOR CELLS, CULTURED; XENOGRAFT MODEL ANTITUMOR ASSAYS;

EID: 0034840040 PISSN: 15257770 EISSN: None Source Type: Journal
DOI: 10.1081/NCN-100002493 Document Type: Conference Paper

Times cited : (18)

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