Synthesis of 3- or 4-phenyl-1,8-naphthyridine derivatives and evaluation of antimycobacterial and antimicrobial activity

Farmaco

Volumn 58, Issue 9, 2003, Pages 859-866

  Badawneh, Muwaffag ^a   Bellini, Laura ^b   Cavallini, Tiziana ^b   Al Jamal, Jalal ^a   Manera, Clementina ^b   Saccomanni, Giuseppe ^b   Ferrarini, Pier Luigi ^b  

^a PHILADELPHIA UNIVERSITY   (Jordan)

^b UNIVERSITY OF PISA   (Italy)

Author keywords

1,8 Naphthyridines; Antimicrobial agents; Antimycobacterial agents; Ethylpiperazinyl; Morpholinyl; Phenylpiperazinyl; Piperidinyl; Tuberculostatic agents

Indexed keywords

1,8 NAPHTHYRIDINE DERIVATIVE; 2,7 BIS(4 ETHYLPIPERAZIN 1 YL) 4 PHENYL 1,8 NAPHTHYRIDINE; 2,7 BIS(4 PHENYLPIPERAZIN 1 YL) 4 PHENYL 1,8 NAPHTHYRIDINE; 2,7 BIS(MORPHOLIN 1 YL) 4 PHENYL 1,8 NAPHTHYRIDINE; 2,7 BIS(PIPERIDIN 1 YL) 4 PHENYL 1,8 NAPHTHYRIDINE; 7 AMINO 2 (MORPHOLIN 1 YL) 4 PHENYL 1,8 NAPHTHYRIDINE; 7 AMINO 4 PHENYL 2 (4 ETHYLPIPERAZIN 1 YL) 1,8 NAPHTHYRIDINE; 7 AMINO 4 PHENYL 2 (4 PHENYLPIPERAZIN 1 YL) 1,8 NAPHTHYRIDINE; 7 AMINO 4 PHENYL 2 (PIPERIDIN 1 YL) 1,8 NAPHTHYRIDINE; 7 CHLORO 2 (MORPHOLIN 1 YL) 4 PHENYL 1,8 NAPHTHYRIDINE; 7 CHLORO 4 PHENYL 2 (4 ETHYLPIPERAZIN 1 YL) 1,8 NAPHTHYRIDINE; 7 CHLORO 4 PHENYL 2 (4 PHENYLPIPERAZIN 1 YL) 1,8 NAPHTHYRIDINE; 7 CHLORO 4 PHENYL 2 (PIPERIDIN 1 YL) 1,8 NAPHTHYRIDINE; 7 HYDROXY 2 (MORPHOLIN 1 YL) 4 PHENYL 1,8 NAPHTHYRIDINE; 7 HYDROXY 4 PHENYL 2 (4 ETHYLPIPERAZIN 1 YL) 1,8 NAPHTHYRIDINE; 7 HYDROXY 4 PHENYL 2 (4 PHENYLPIPERAZIN 1 YL) 1,8 NAPHTHYRIDINE; 7 HYDROXY 4 PHENYL 2 (PIPERIDIN 1 YL) 1,8 NAPHTHYRIDINE; 7 METHOXY 4 PHENYL 2 (4 ETHYLPIPERAZIN 1 YL) 1,8 NAPHTHYRIDINE; 7 METHOXY 4 PHENYL 2 (4 PHENYLPIPERAZIN 1 YL) 1,8 NAPHTHYRIDINE; 7 METHOXY 4 PHENYL 2 (PIPERIDIN 1 YL) 1,8 NAPHTHYRIDINE; ALKYL GROUP; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG SCREENING; DRUG SYNTHESIS; ESCHERICHIA COLI; GRAM NEGATIVE BACTERIUM; GRAM POSITIVE BACTERIUM; MINIMUM INHIBITORY CONCENTRATION; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; STAPHYLOCOCCUS AUREUS;

EID: 0141788046     PISSN: 0014827X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-827X(03)00144-7     Document Type: Article

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