New synthetic approach to coumarino[4,3-b]pyridine systems and potential cytotoxic evaluation

Medicinal Chemistry Research

Volumn 23, Issue 5, 2014, Pages 2615-2621

  Hamama, Wafaa S ^a   Ibrahim, Mona E ^a   Metwalli, Asmaa E ^a   Zoorob, Hanafi H ^a  

^a Mansoura University   (Egypt)

Author keywords

Annulation; Biselectrophiles; Coumarin; Cytotoxic activity (in vitro); Regioselective

Indexed keywords

11 BENZYLIDENE 8,9,10,11 TETRAHYDRO 7 PHENYLCOUMARINO[4,3 B]QUINOLIN 6 ONE; 1H COUMARINO [4,3 B]PYRIDINE 2,4,5(3H) TRIONE; 2 (4 NITROPHENYL) 4 PHENYL 5H COUMARINO[4,3B]PYRIDIN 5 ONE; 4 AMINO 3 ((4 AMINO 2 OXO 2H COUMARIN 3 YL) (4 CHLOROPHENYL) METHYL) 2H COUMARIN 2 ONE; 4 PHENYL 2 STYRYL 5H COUMARINO [4,3 B]PYRIDIN 5 ONE; BENZYLIDENE DERIVATIVE; COUMARIN DERIVATIVE; CYANOACRYLATE; CYCLOHEXANONE; CYTOTOXIC AGENT; KETONE; PYRIDINE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CELL VIABILITY; CYTOTOXICITY; DRUG STRUCTURE; DRUG SYNTHESIS; EHRLICH ASCITES TUMOR CELL; IC 50; IN VITRO STUDY; POLYMERIZATION;

EID: 84898796197     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-013-0859-y     Document Type: Article

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