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Volumn 345, Issue 1, 2012, Pages 49-56
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Synthesis and cytotoxicity studies of novel 2-hydrazonylpyrido[2,3-b] pyrazin-3(4H)-ones
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Author keywords
2 Hydrazonylpyrido 2,3 b pyrazin 3(4H) ones; Anticancer activity; Apoptosis
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Indexed keywords
2 [2 (2 HYDROXY 3 (2 METHYLALLYL)BENZYLIDENE)HYDRAZINYL]4 (4 METHOXYPHENYL)PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 (4 METHOXYPHENYL)PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (2,4 DIHYDROXYBENZYLIDENE)HYDRAZINYL] 4 (4 METHOXYPHENYL)PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (2,4 DIHYDROXYBENZYLIDENE)HYDRAZINYL] 4 [4 (TRIFLUOROMETHOXY)PHENYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 2 HYDROXY 5 ISOPROPYLBENZYLIDENE)HYDRAZINYL] 4 PHENYLPYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 2 HYDROXY 5 METHYLBENZYLIDENE)HYDRAZINYL] 4 (4 METHOXYPHENYL)PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 2 HYDROXY 5 METHYLBENZYLIDENE)HYDRAZINYL] 4 [4 (TRIFLUOROMETHOXY)PHENYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 2 HYDROXY 5 METHYLBENZYLIDENE)HYDRAZINYL] 4 PHENYLPYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 (4 METHOXYPHENYL)PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 [4 (TRIFLUOROMETHOXY)PHENYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 PHENYLPYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 5 TERT BUTYL 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 (4 METHOXYPHENYL)PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 5 TERT BUTYL 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 [4 (TRIFLUOROMETHOXY)PHENYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3 ALLYL 5 TERT BUTYL 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 PHENYLPYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3,5 DI TERT BUTYL 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 [4 (TRIFLUOROMETHOXY)PHENYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (3,5 DI TERT BUTYL 2 HYDROXYBENZYLIDENE)HYDRAZINYL]4 PHENYLPYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (4 CHLORO 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 (4 METHOXYPHENYL)PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 (4 CHLORO 2 HYDROXYBENZYLIDENE)HYDRAZINYL] 4 [4 (TRIFLUOROMETHOXY)PHENYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 [2 HYDROXY 3 (2 METHYLALLYL)BENZYLIDENE]HYDRAZINYL] 4 [4 (TRIFLUOROMETHOXY)PHENYL)PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 [2 HYDROXY 3 (2 METHYLALLYL)BENZYLIDENE]HYDRAZINYL] 4 PHENYLPYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 [4 (4 CHLOROBENZYLOXY) 2 HYDROXYBENZYLIDENE]HYDRAZINYL] 4 PHENYLPYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
2 [2 [4 (BENZYLOXY) 2 HYDROXYBENZYLIDENE]HYDRAZINYL] 4 [4 (TRIFLUOROMETHOXY)PHENYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
4 (4 METHOXYPHENYL) 2 [2 (2,3,4 TRIHYDROXYBENZYLIDENE)HYDRAZINYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
4 PHENYL 2 [2 (2,3,4 TRIHYDROXYBENZYLIDENE)HYDRAZINYL]PYRIDO[2,3 B]PYRAZIN 3 (4H)ONE;
ANTINEOPLASTIC AGENT;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CONTROLLED STUDY;
CYTOTOXICITY;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IC 50;
IN VITRO STUDY;
PRIORITY JOURNAL;
ANTINEOPLASTIC AGENTS;
CELL SURVIVAL;
CHEMISTRY TECHNIQUES, SYNTHETIC;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DESIGN;
HT29 CELLS;
HUMANS;
INHIBITORY CONCENTRATION 50;
MOLECULAR STRUCTURE;
PYRAZINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84862909090
PISSN: 03656233
EISSN: 15214184
Source Type: Journal
DOI: 10.1002/ardp.201100103 Document Type: Article |
Times cited : (8)
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References (16)
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