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Volumn 79, Issue , 2014, Pages 446-454
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Design, synthesis and biological evaluation of some novel substituted quinazolines as antitumor agents
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Author keywords
In vitro antitumor evaluation; NCI; Quinazoline; Selective activity; Synthesis
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Indexed keywords
11 CHLORO 7 PARA TOLYL 2,3 DIHYDRO [1,2,4,5] TETRAZEPINO [2,3 C] QUINAZOLIN 4 (5H) ONE;
2 AMINO N (6 CHLORO 4 OXO 2 PARA TOLYLQUINAZOLIN 3(4H) YL)ACETAMIDE;
2 CHLORO N (6 CHLORO 4 OXO 2 PARA TOLYLQUINAZOLIN 3 (4H) YL)ACETAMIDE;
3 (BENZYLIDENEAMINO) 6 CHLORO 2 PARA TOLYLQUINAZOLIN 4 (3H) ONE;
3 AMINO 6 CHLORO 2 PARA TOLYLQUINAZOLIN 4 (3H) ONE;
5 CHLORO 2 (4 METHYLBENZAMIDO) N (PYRIDIN 2 YL)BENZAMIDE;
5 CHLORO 2 (4 METHYLBENZAMIDO) N PHENYL BENZAMIDE;
6 CHLORO 2 PARA TOLYL 4H BENZO[D][1,3] OXAZIN 4 ONE;
6 CHLORO 2 PARA TOLYLQUINAZOLIN 4 (3H) ONE;
6 CHLORO 2 PARA TOLYLQUINAZOLIN 4 (3H) THIONE;
6 CHLORO 4 HYDRAZINO 2 PARA TOLYLQUINAZOLINE;
9 CHLORO 5 PARA TOLYL [1,2,4] TRIAZOLO [4,3 C] QUINAZOLINE 3 THIOL;
9 CHLORO 5 PARA TOLYLTETRAZOLO [1,5 C] QUINAZOLINE;
ANTINEOPLASTIC AGENT;
ETHYL 2 (5 CHLORO 2 (4 METHYLBENZAMIDO)BENZAMIDO)ACETATE;
ETHYL 2 (6 CHLORO 4 OXO 2 PARA TOLYLQUINAZOLIN 3 (4H) YL)ACETATE;
FLUOROURACIL;
N (4 CHLORO 2 (HYDRAZINECARBONYL)PHENYL) 4 METHYLBENZAMIDE;
N (6 CHLORO 4 OXO 2 PARA TOLYLQUINAZOLIN 3 (4H) YL) 2 HYDRAZINYLACETAMIDE;
N BENZYL 5 CHLORO 2 (4 METHYLBENZAMIDO)BENZAMIDE;
QUINAZOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CANCER CELL CULTURE;
CANCER INHIBITION;
CENTRAL NERVOUS SYSTEM TUMOR;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
LIPOPHILICITY;
LUNG NON SMALL CELL CANCER;
OVARY CANCER;
RECTUM CANCER;
CELL PROLIFERATION;
CHEMICAL STRUCTURE;
CHEMISTRY;
CYCLIZATION;
DOSE RESPONSE;
DRUG EFFECTS;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
TUMOR CELL LINE;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
CELL PROLIFERATION;
CYCLIZATION;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DESIGN;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
MOLECULAR STRUCTURE;
QUINAZOLINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84899060225
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2014.04.029 Document Type: Article |
Times cited : (66)
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References (33)
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