Synthesis and microbiological activity of some N-(2-hydroxy-4-substitutedphenyl)benzamides, phenylacetamides and furamides as the possible metabolites of antimicrobial active benzoxazoles

Aki-Sener E., Bingol K., Temiz-Arpaci O., Yalcin I., Altanlar N.

FARMACO, cilt.57, sa.6, ss.451-456, 2002 (SCI-Expanded) identifier identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 57 Sayı: 6
  • Basım Tarihi: 2002
  • Doi Numarası: 10.1016/s0014-827x(02)01226-0
  • Dergi Adı: FARMACO
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Index Chemicus (IC)
  • Sayfa Sayıları: ss.451-456
  • Anahtar Kelimeler: benzamides, phenylacetamides, furamides, benzoxazoles, antimicrobial activity, BENZIMIDAZOLES, DERIVATIVES, AGENTS, OXAZOLO(4,5-B)PYRIDINES, BENZOTHIAZOLES, MITOCHONDRIA, ANTIFUNGAL
  • Ankara Üniversitesi Adresli: Evet

Özet

The synthesis of some N-(2-hydroxy-4-substitutedphenyl)benzamides, phenylacetamides and furamides as the possible metabolites of benzoxazoles (II1-15) was performed in order to determine their in vitro antimicrobial activity against three Gram-positive bacteria, two Gram-negative bacteria and the fungus Candida albicans and their activities were compared with several control drugs. The compounds II11, II12, and II13 were found active at a MIC value of 12.5 mug/ml against the Gram-negative microorganism Pseudomonas aeruginosa. Most of the compounds show antibacterial activity at MIC a value of 25 mug/ml against the Gram-positive bacteria Staphylococcus aureus. For the antifungal activity against C. albicans, compound II10 was found more active than the other derivatives. The antimicrobial activity of some of these benzamides, phenylacetamides (II1 and II10) which are the possible metabolites of benzoxazoles, was also compared to their corresponding cyclic analogues III-IV. Compound II10 possesses two dilutions better antifungal activity than its cyclic analogue, benzoxazole IV, against C. albicans. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.