Synthesis, characterisation and biological activity of novel 4-thiazolidinones, 1,3,4-oxadiazoles and some related compounds

Kucukguzel Ş. G., Oruc E., Rollas S., Sahin F., Ozbek A.

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, cilt.37, sa.3, ss.197-206, 2002 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 37 Sayı: 3
  • Basım Tarihi: 2002
  • Doi Numarası: 10.1016/s0223-5234(01)01326-5
  • Dergi Adı: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.197-206
  • Anahtar Kelimeler: 4-thiazolidinone, 1,3,4-oxadiazole, hydrazide-hydrazone, thiosemicarbazide, antimycobacterial activity, BACTEC 460 radiometric system, ANTICONVULSANT ACTIVITY, ANTIMICROBIAL ACTIVITY, ANTIFUNGAL ACTIVITY, DERIVATIVES
  • Marmara Üniversitesi Adresli: Evet

Özet

Two novel series of 4-thiazolidinone derivatives namely 2-substituted-3-{[4-(4-methoxybenzoylamino)benzoyl]amino}-4-thiazolidinones (7a-e) and 2-[4-(4-methoxybenzoylamino)benzoylhydrazono]-3-alkyl-4-thiazolidinones (5a-c) together with 2-[4-(4-methoxybenzoylamino)phenyl]-5-(substituted phenyl)amino-1,3,4-oxadiazoles (6a-c) have been synthesised as title compounds. N-1-[4-(4-methoxybenzoylamino)benzoyl]-N-2-substituted methylene hydrazines (3a-e) and 1-[4-(4-methoxybenzoylamino)benzoyl]4-substituted phenyl thiosemicarbazides (4a-f) were also prepared and used as intermediate to give the title compounds. All synthesised compounds were screened for their antimycobacterial activity against Mycobacterium tuberculosis H37Rv and antimicrobial activities against various bacteria and fungi. Compounds 7a and 7b were found as the most active derivatives demonstrating 90 and 98% inhibition of mycobacterial growth of M. tuberculosis H37Rv, in the primary screen at 6.25 mug mL(-1), respectively. However, level 11 assay revealed that the MIC values were not less than 6.25 mug mL(-1). None of the compounds showed significant antimicrobial activity against the microorganisms used whereas 3a and 7a inhibited the growth of several bacteria and fungi. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.