Synthesis, antimicrobial, and antioxidant activities of some new indole analogues containing pyrimidine and fused pyrimidine systems

Medicinal Chemistry Research

Volumn 21, Issue 11, 2012, Pages 3809-3817

  Raghunath, Saundane Anand ^a   Manjunatha, Yarlakatti ^a   Rayappa, Kalpana ^a  

^a GULBARGA UNIVERSITY   (India)

Author keywords

Antimicrobial; Antioxidant; Indole; Pyrazolopyrimidine; Tetrazolopyrimidines

Indexed keywords

4 (2' PHENYL 1H INDOL 3' YL) 6 HYDRAZINO 1H PYRAZOLO[3,4 D]PYRIMIDIN 3 AMINE; 4 (5' CHLORO 2' PHENYL 1H INDOL 3' YL) 6 HYDRAZINO 1H PYRAZOLO[3,4 D]PYRIMIDIN 3 AMINE; 4 (5' METHYL 2' PHENYL 1H INDOL 3' YL) 6 HYDRAZINO 1H PYRAZOLO[3,4 D]PYRIMIDIN 3 AMINE; 5 (2' PHENYL 1H INDOL 3' YL)DITETRAZOLO[1,5 A;1' ,5' C]PYRIMIDIN 6 CARBONITRILE; 5 (5' CHLORO 2' PHENYL 1H INDOL 3' YL)DITETRAZOLO[1,5 A;1',5', C]PYRIMIDIN 6 CARBONITRILE; 5 (5' METHYL 2' PHENYL 1H INDOL 3' YL)DITETRAZOLO[1,5 A;1',5', C]PYRIMIDIN 6 CARBONITRILE; 6 (2' PHENYL 1H INDOL 3' YL) 2 4 DITHIOXO 1,2,3,4, TETRAHYDROPYRIMIDIN 5 CARBONITRILE; 6 (2' PHENYL 1H INDOL 3' YL) 2,4 DIHYDRAZINYLPYRIMIDIN 5 CARBONITRILE; 6 (2' PHENYL 1H INDOL 3' YL) 4 OXO 1,2,3,4 TETRAHYDRO 2 THIOPYRIMIDIN 5 CARBONITRILE; 6 (5' CHLORO 2' PHENYL 1H INDOL 3' YL) 2 4 DITHIOXO 1,2,3,4, TETRAHYDROPYRIMIN 5 CARBONITRILE; 6 (5' CHLORO 2' PHENYL 1H INDOL 3' YL) 2,4 DIHYDRAZINYLPYRIMIDIN 5 CARBONITRILE; 6 (5' CHLORO 2' PHENYL 1H INDOL 3' YL) 4 OXO 1,2,3,4 TETRAHYDRO 2 THIOXOPYRIMIDIN 5 CARBONITRILE; 6 (5' METHYL 2' PHENYL 1H INDOL 3' YL) 2 4 DITHIOXO 1,2,3,4 TETRAHYDROPYRIMIDIN 5 CARBONITRILE; 6 (5' METHYL 2' PHENYL 1H INDOL 3' YL) 4 OXO 1,2,3,4 TETRAHYDRO2 THIOXOPYRIMIDIN 5 CARBONITRILE; 6 (5' METHYL 2' PHENYL 1H INDOLE 3' YL) 2,4DIHYDRAZINYLPYRIMIDIN 5 CARBONITRILE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ANTIOXIDANT ACTIVITY; ARTICLE; ASPERGILLUS NIGER; CYCLIZATION; DRUG SYNTHESIS; FUNGUS GROWTH; GROWTH INHIBITION; KLEBSIELLA PNEUMONIAE; LIPID OXIDATION; NONHUMAN; PSEUDOMONAS AERUGINOSA; STAPHYLOCOCCUS AUREUS;

EID: 84871424272     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-011-9915-7     Document Type: Article

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