SCOPUS 정보 검색 플랫폼

Volumn 345, Issue 4, 2012, Pages 314-322

Synthesis and antimicrobial evaluation of new pyrano[4,3-b]pyran and pyrano[3,2-c]chromene derivatives bearing a 2-thiophenoxyquinoline nucleus

(3) Makawana, Jigar A a Patel, Manish P a Patel, Ranjan G a

a SARDAR PATEL UNIVERSITY (India)

Author keywords

2 Thiophenoxyquinoline; Chromene; In vitro antimicrobial activity; Pyran

Indexed keywords

2 AMINO 4 [2 (4 CHLOROPHENYLTHIO) 6 METHOXYQUINOLIN 3 YL] 5 OXO 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (4 CHLOROPHENYLTHIO) 6 METHOXYQUINOLIN 3 YL] 5 OXO 7 METHYL 4,5 DIHYDROPYRANO(4,3 B)PYRAN 3 CARBONITRILE; 2 AMINO 4 [2 (4 CHLOROPHENYLTHIO) 6 METHOXYQUINOLIN 3 YL] 5 OXO 9 METHYL 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (4 CHLOROPHENYLTHIO) 6 METHYLQUINOLIN 3 YL] 5 OXO 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (4 CHLOROPHENYLTHIO) 6 METHYLQUINOLIN 3 YL] 5 OXO 9 METHYL 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (4 CHLOROPHENYLTHIO)QUINOLIN 3 YL] 5 OXO 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (4 CHLOROPHENYLTHIO)QUINOLIN 3 YL] 5 OXO 7 METHYL 4,5 DIHYDROPYRANO(4,3 B)PYRAN 3 CARBONITRILE; 2 AMINO 4 [2 (4 CHLOROPHENYLTHIO)QUINOLIN 3 YL] 5 OXO 9 METHYL 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (4 METHYLPHENYLTHIO) 6 METHOXYQUINOLIN 3 YL] 5 OXO 7 METHYL 4,5 DIHYDROPYRANO(4,3 B)PYRAN 3 CARBONITRILE; 2 AMINO 4 [2 (4 METHYLPHENYLTHIO) 6 METHYLQUINOLIN 3 YL] 5 OXO 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (4 METHYLPHENYLTHIO) 6 METHYLQUINOLIN 3 YL] 5 OXO 7 METHYL 4,5 DIHYDROPYRANO(4,3 B)PYRAN 3 CARBONITRILE; 2 AMINO 4 [2 (4 METHYLPHENYLTHIO)QUINOLIN 3 YL] 5 OXO 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (4 METHYLPHENYLTHIO)QUINOLIN 3 YL] 5 OXO 7 METHYL 4,5 DIHYDROPYRANO(4,3 B)PYRAN 3 CARBONITRILE; 2 AMINO 4 [2 (4 METHYLPHENYLTHIO)QUINOLIN 3 YL] 5 OXO 9 METHYL 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO) 6 METHOXYQUINOLIN 3 YL] 5 OXO 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO) 6 METHOXYQUINOLIN 3 YL] 5 OXO 9 METHYL 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO) 6 METHOXYQUINOLIN-3 YL] 5 OXO 7 METHYL 4,5 DIHYDROPYRANO(4,3 B)PYRAN 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO) 6 METHYLQUINOLIN 3 YL] 5 OXO 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO) 6 METHYLQUINOLIN 3 YL] 5 OXO 7 METHYL 4,5 DIHYDROPYRANO(4,3 B)PYRAN 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO) 6 METHYLQUINOLIN 3 YL] 5 OXO 9 METHYL 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO)QUINOLIN 3 YL] 5 OXO 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO)QUINOLIN 3 YL] 5 OXO 7 METHYL 4,5 DIHYDROPYRANO(4,3 B)PYRAN 3 CARBONITRILE; 2 AMINO 4 [2 (PHENYLTHIO)QUINOLIN 3 YL] 5 OXO 9 METHYL 4,5 DIHYDROPYRANO(3,2 C)CHROMENE 3 CARBONITRILE; AMPICILLIN; ANTIBIOTIC AGENT; ANTIFUNGAL AGENT; CHROMENE DERIVATIVE; GRISEOFULVIN; NORFLOXACIN; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ABSORPTION; ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ARTICLE; ASPERGILLUS FUMIGATUS; BACILLUS SUBTILIS; BACTERIAL STRAIN; BROTH DILUTION; CANDIDA ALBICANS; CATALYST; CHEMICAL REACTION; CLOSTRIDIUM TETANI; COLONY FORMING UNIT; DRUG SCREENING; DRUG SYNTHESIS; ESCHERICHIA COLI; IN VITRO STUDY; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; PRIORITY JOURNAL; ROOM TEMPERATURE; SALMONELLA TYPHI; STREPTOCOCCUS PNEUMONIAE; STRUCTURE ACTIVITY RELATION; THIN LAYER CHROMATOGRAPHY; VIBRIO CHOLERAE;

ANTI-INFECTIVE AGENTS; BENZOPYRANS; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; OXYQUINOLINE; PYRANS; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84859732160 PISSN: 03656233 EISSN: 15214184 Source Type: Journal
DOI: 10.1002/ardp.201100203 Document Type: Article

Times cited : (67)

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