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Synthesis of some N-alkoxycarbonyl-N"-benzoyl-benzamidrazones(p- toluamidrazones) and 1,3,5-trisubstituted 1,2,4-triazole derivatives from N-benzoylimidates and their antimicrobial and anticancer screening studies

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info:eu-repo/semantics/closedAccess

Date

2007

Author

Bekircan, Olcay
Kahveci, Bahittin
Özgümüş, Osman Birol

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Citation

Bekircan, O., Kahveci, B. & Özgümüş, B. (2007). Synthesis of Some N-Alkoxycarbonyl-N"-benzoyl-benzamidr-azones(p-toluamidrazones) and 1,3,5-Trisubstituted 1,2,4-Triazole Derivatives from N-Benzoylimidates and their Antimicrobial and Anticancer Screening Studies. Chinese Journal of Chemistry, 25(12), 1871-1877. http://doi.org/10.1002/cjoc.200790345

Abstract

Some new N-alkoxycarbonyl-N?-benzoyl-benzamidrazones (p-toluamidrazones) 3a-3d, and 1,3,5-trisubstituted 1,2,4-triazole 4a-4h derivatives by starting from N-benzoylbenzimidates or N-benzoyl-p-toluimidates. The structures of compounds 3 and 4 were established on the basis of elemental analyses, IR, 1H NMR, 13C NMR and UV data. Antimicrobial experiments of the compounds performed by using agar-well diffusion and broth microdilution methods revealed that only compounds 3a-3d, 4a and 4b showed inhibitory effect only on Candida albicans ATCC 60193. However, compound 4b had also specific antibacterial activity against Staphylococcus aureus ATCC 25923. The other compounds showed neither antifungal nor antibacterial activities. Compounds 3a, 4a and 4b have been screened on three human tumor cell lines, breast cancer (MCF7), non small cell lung cancer (NCI-H460), and CNS cancer (SF-268) at the National Cancer Institute (NCI), USA, which were found to exhibit low antiproliferative activity. © 2007 SIOC, CAS, & Wiley-VCH Verlag GmbH & Co. KGaA.

Source

Chinese Journal of Chemistry

Volume

25

Issue

12

URI

https://doi.org/10.1002/cjoc.200790345
https://hdl.handle.net/11436/3955

Collections

  • FEF, Biyoloji Bölümü Koleksiyonu [588]
  • FEF, Kimya Bölümü Koleksiyonu [474]
  • Scopus İndeksli Yayınlar Koleksiyonu [5931]



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