Quantitative structure-activity relationships using comparative molecular field analysis studies on 2-(p-substituted benzyl)-5-(substituted carbonylamino)benzoxazoles as antibacterial agents against Staphylococcus aureus

Yildiz-Oren İ., Tekiner-Gulbas B., ARPACI Ö., Yalcin I., Aki-Sener E.

ASIAN JOURNAL OF CHEMISTRY, cilt.16, sa.3-4, ss.1359-1366, 2004 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 16 Sayı: 3-4
  • Basım Tarihi: 2004
  • Dergi Adı: ASIAN JOURNAL OF CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1359-1366
  • Anahtar Kelimeler: 3D-QSAR comparative molecular field analysis, antibacterial activity, 2-benzylbenzoxazole, Stapyhlococcus aureus, MICROBIOLOGICAL ACTIVITY, ANTIMICROBIAL ACTIVITIES, DERIVATIVES, BENZIMIDAZOLES, BENZOXAZOLES, BENZOTHIAZOLES, UK-1, OXAZOLO(4,5-B)PYRIDINES, ANTIFUNGAL, RESISTANCE
  • Ankara Üniversitesi Adresli: Evet

Özet

The 3D-QSAR studies using comparative molecular, field analysis (CoMFA) approach on a set of 2-(p-substituted benzyl)-5-(substituted carbonylarnino)benzoxazoles as antibacterial agents against Staphylococcus aureus by considering the steric and electrostatic influences have been presented. The CoMFA analysis gave cross- validated r(2) value of 0.480 and non cross-validated r(2) = 0.950 with an optimized component of 4. The model deduced from this investigation provides underlying structural requirements and good predictive ability, which could aid the new antibacterial agents for Staphylococcus aureus prior to their synthesis.