Facile synthesis of novel quinoline derivatives as anticancer agents

Medicinal Chemistry Research

Volumn 23, Issue 6, 2014, Pages 2727-2735

  Marganakop, Sheetal Babu ^a   Kamble, Ravindra Ramappa ^a   Hoskeri, Joy ^b   Prasad, D Jagadish ^c   Meti, Gangadhar Yamanappa ^a  

^a KARNATAK UNIVERSITY   (India)

^b HSR   (India)

^c MANGALORE UNIVERSITY   (India)

Author keywords

Anticancer activity; Breast cancer cell line MCF7; Cervix cancer cell line HeLa; DNA cleavage; Quinoline

Indexed keywords

ACETAMIDE DERIVATIVE; ANTINEOPLASTIC AGENT; DOXORUBICIN; N [4 ACETYL 4,5 DIHYDRO 5 (7 BROMO TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (7 CHLORO TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (7 METHOXY TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (7 METHYL TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (7,8 DIMETHOXY TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (7,8,9 SUBSTITUTED TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE DERIVATIVE; N [4 ACETYL 4,5 DIHYDRO 5 (8 METHOXY TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (8 METHYL TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (9 METHOXY TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (9 METHYL TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; N [4 ACETYL 4,5 DIHYDRO 5 (TETRAZOLO[1,5 A]QUINOLIN 4 YL) 1,3,4 THIADIAZOL 2 YL]ACETAMIDE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; BREAST CANCER; CELL GROWTH; CELL STRAIN MCF 7; CONCENTRATION RESPONSE; CONTROLLED STUDY; CYTOTOXICITY; DNA CLEAVAGE; DNA ISOLATION; DRUG SYNTHESIS; HELA CELL; HUMAN; HUMAN CELL; IN VITRO STUDY; ONE POT SYNTHESIS; UTERINE CERVIX CANCER;

EID: 84898926991     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-013-0855-2     Document Type: Article

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