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Volumn 51, Issue 1, 2004, Pages 147-156
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Synthesis, reactions and antimicrobial activity of some new indolyl-1,3,4-oxadiazole, triazole and pyrazole derivatives
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Author keywords
3 Indolyloxadiazoles; 3 Indolytriazoles and pyrazoles; Monoamine oxidase
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Indexed keywords
(1 BENZYL 1H INDOL 3 YL)(3,5 DIMETHYLPYRAZOL 1 YL)METHANONE;
1 (1 BENZYL 1H INDOL 3 YL)CARBONYL 1,2 DIHYDRO 5 METHYLPYRAZOL 3 ONE;
1 BENZYL 1H INDOLE 3 CARBOHYDRAZIDE;
1 BENZYL 1H INDOLE 3 CARBONYLAZIDE;
1 BENZYL 3 MORPHOLINOCARBONYLAMINO 1H INDOLE;
1 BENZYL 3 PIPERIDINOCARBONYLAMINO 1H INDOLE;
1,3 BIS(1 BENZYL 1H INDOL 3 YL)UREA;
2 (1 BENZYL 1H INDOL 3 YL) 1,3,4 OXADIAZOL 5(4H) ONE;
2 (1 BENZYL 1H INDOL 3 YL) 1,3,4 OXADIAZOLE;
2 (1 BENZYL 1H INDOL 3 YL) 1,3,4 OXADIAZOLE 5(4H) THIONE;
3 (1 BENZYL 1H INDOL 3 YL) 4 PHENYL 1,2,4 TRIAZOLE 2 THIONE;
3 (1BENZYL 1H INDOL 3 YL) 6 PHENYL 7H 1,2,4 TRIAZOLO[3,4 B][1,3,4]THIADIAZINE;
4 ACETYL 4,5 DIHYDRO 2 (1 BENZYL 1H INDOL 3 YL) 5 PHENYL 1,3,4 OXADIAZOLE;
4 AMINO 3 (1 BENZYL 1H INDOL 3 YL) 1,2,4 TRIAZOL 5(1H) ONE;
4 AMINO 3 (1 BENZYL 1H INDOL 3 YL) 1,2,4 TRIAZOLE 5(1H) THIONE;
5 (2' DIETHYLAMINOETHYLTHIO) 3 (1 BENZYL 1H INDOL 3 YL) 4 PHENYL 1,2,4 TRIAZOLE;
5 (2' MORPHOLINOETHYLTHIO) 2 (1 BENZYL 1H INDOL 3 YL) 1,3,4 OXADIZOLE;
5 (2' MORPHOLINOETHYLTHIO) 3 (1 BENZYL 1H INDOL 3 YL) 4 PHENYL 1,2,4 TRIAZOLE;
5 AMINO 1 (1 BENZYL 1H INDOL 3 YL)CARBONYL 1H PYRAZOLE 4 CARBONITRILE;
ANTIINFECTIVE AGENT;
ETHYL 1 BENZYL 1H INDOLE 3 CARBOXYLATE;
ETHYL 5 AMINO 1 (1 BENZYL 1H INDOL 3 YL)CARBONYL 1H PYRAZOLE 4 CARBOXYLATE;
ETHYL N (1 BENZYL 1H INDOL 3 YL)CARBAMATE;
ISOPROPYL N (1 BENZYL 1H INDOL 3 YL)CARBAMATE;
N1 (1 BENZYL 1H INDOL 3 OYL) N4 PHENYLTHIOSEMICARBAZIDE;
N1 (1 BENZYL 1H INDOL 3 YL) N3 (2 HYDROXYETHYL)UREA;
N4 (1 BENZYL 1H INDOL 3 YL)SEMICARBAZIDE;
OXADIAZOLE DERIVATIVE;
PYRAZOLE DERIVATIVE;
TRIAZOLE DERIVATIVE;
UNCLASSIFIED DRUG;
ANTIBACTERIAL ACTIVITY;
ANTIFUNGAL ACTIVITY;
ANTIMICROBIAL ACTIVITY;
ARTICLE;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG SCREENING;
DRUG SYNTHESIS;
IN VITRO STUDY;
NONHUMAN;
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EID: 2142806013
PISSN: 00094536
EISSN: None
Source Type: Journal
DOI: 10.1002/jccs.200400023 Document Type: Article |
Times cited : (86)
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References (19)
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