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Volumn 331, Issue 11, 1998, Pages 352-358
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5-Substituted 2-bromoindolo[3,2-b]quinoxalines. A class of potential antitumor agents with cdc25 phosphatase inhibitory properties
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Author keywords
Antitumor testing; cdc kinase and phosphatase; Indolo 3.2 b quinoxaline
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Indexed keywords
2 (2 BROMOINDOLO[3,2 B]QUINOXALIN 5 YL) N [[(CYCLOHEXYLAMINO)THIOXOMETHYL]AMINO]ETHANAMIDE;
CYTOSTATIC AGENT;
MELPHALAN;
PHOSPHOPROTEIN PHOSPHATASE;
PROTEIN KINASE;
QUINOXALINE DERIVATIVE;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CANCER CELL CULTURE;
CANCER INHIBITION;
CONTROLLED STUDY;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
LC 50;
PRIORITY JOURNAL;
ANTINEOPLASTIC AGENTS;
FEMALE;
HUMANS;
MALE;
PHOSPHORIC MONOESTER HYDROLASES;
QUINOXALINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
TUMOR CELLS, CULTURED;
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EID: 0032444828
PISSN: 03656233
EISSN: None
Source Type: Journal
DOI: 10.1002/(SICI)1521-4184(199811)331:11<352::AID-ARDP352>3.0.CO;2-2 Document Type: Article |
Times cited : (22)
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References (7)
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