Novel furanylarylene arylsulfonylindolesulfonamides: Synthesis and their antibacterial evaluation

Chemical and Pharmaceutical Bulletin

Volumn 57, Issue 6, 2009, Pages 591-596

  Ramalingan, Chennan ^a   Lee, In Sook ^a   Kwak, Young Woo ^a  

^a Kyungpook National University   (South Korea)

Author keywords

Antibacterial activity; Chlorosulfonylation; Condensation; Diarylfuran; Indole; Stille cross coupling

Indexed keywords

BENZENE DERIVATIVE; METHYL GROUP; N,N' [4,4' (FURAN 2,5 DIYL)BIS(3 METHYL 4,1 PHENYLENE)]BIS[1 (4 BROMOPHENYLSULFONYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(3 METHYL 4,1 PHENYLENE)]BIS[1 (4 CHLOROPHENYLSULFONYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(3 METHYL 4,1 PHENYLENE)]BIS[1 (4 METHOXYPHENYLSULFONYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(3 METHYL 4,1 PHENYLENE)]BIS[1 (4 METHYLPHENYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(3 METHYL 4,1 PHENYLENE)]BIS[1 (PHENYLSULFONYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(4,1 PHENYLENE)]BIS[1 (4 BROMOPHENYLSULFONYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(4,1 PHENYLENE)]BIS[1 (4 CHLOROPHENYLSULFONYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(4,1 PHENYLENE)]BIS[1 (4 METHOXYPHENYLSULFONYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(4,1 PHENYLENE)]BIS[1 (4 METHYLPHENYL) 1H INDOLE 3 SULFONAMIDE]; N,N' [4,4' (FURAN 2,5 DIYL)BIS(4,1 PHENYLENE)]BIS[1 (PHENYLSULFONYL) 1H INDOLE 3 SULFONAMIDE]; STREPTOMYCIN; SULFONAMIDE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; BACILLUS SUBTILIS; BROMINATION; CONTROLLED STUDY; DILUTION; DRUG SCREENING; DRUG SYNTHESIS; ENTEROCOCCUS FAECALIS; ESCHERICHIA COLI; KLEBSIELLA PNEUMONIAE; NONHUMAN; POLYMERIZATION; PSEUDOMONAS AERUGINOSA; REDUCTION; STAPHYLOCOCCUS AUREUS; STILLE REACTION;

ANTI-BACTERIAL AGENTS; BACTERIA; INDICATORS AND REAGENTS; INDOLES; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; MICROBIAL SENSITIVITY TESTS; STRUCTURE-ACTIVITY RELATIONSHIP; SULFONAMIDES;

EID: 66949169954     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.57.591     Document Type: Article

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