Design, synthesis and antifungal activity of some new imidazole and triazole derivatives

Archiv der Pharmazie

Volumn 344, Issue 10, 2011, Pages 658-665

  Rezaei, Zahra ^a   Khabnadideh, Soghra ^a   Zomorodian, Kamiar ^b   Pakshir, Kyvan ^b   Kashi, Giti ^a   Sanagoei, Narges ^a   Gholami, Sanaz ^a  

^a SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Antifungal activity; Docking; Imidazole; Triazole

Indexed keywords

1,2,4 TRIAZOLE DERIVATIVE; ANTIFUNGAL AGENT; BENZIMIDAZOLE; BENZOTRIAZOLE DERIVATIVE; CYTOCHROME P450; FLUCONAZOLE; ITRACONAZOLE; STEROL 14ALPHA DEMETHYLASE INHIBITOR;

ANTIFUNGAL ACTIVITY; ARTICLE; ASPERGILLUS FLAVUS; CANDIDA ALBICANS; CANDIDA DUBLINIENSIS; CANDIDA GLABRATA; CANDIDA PARAPSILOSIS; CANDIDA TROPICALIS; CHEMICAL STRUCTURE; DRUG DESIGN; DRUG SYNTHESIS; ENERGY; ENZYME ACTIVE SITE; EPIDERMOPHYTON FLOCCOSUM; IN VITRO STUDY; MASS SPECTROMETRY; MICROSPORUM CANIS; MICROSPORUM GYPSEUM INFECTION; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION; TRICHOPHYTON MENTAGROPHYTES;

14-ALPHA DEMETHYLASE INHIBITORS; ANTIFUNGAL AGENTS; DRUG DESIGN; FUNGI; IMIDAZOLES; LIGANDS; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; PROTEIN BINDING; STEROL 14-DEMETHYLASE; STRUCTURE-ACTIVITY RELATIONSHIP; TRIAZOLES;

EID: 80053945104     PISSN: 03656233     EISSN: 15214184     Source Type: Journal    
DOI: 10.1002/ardp.201000357     Document Type: Article

References (16)

1. S. K. Fridkin, W. R. Jarvis, Clin. Microbiol. Rev. 1996, 9, 499-511.
2. J. R. Wingard, H. Leather, Biol. Blood Marrow Transplant. 2004, 10, 73-90.
3. M. M. Canuto, F. G. Rodero, Lancet Infect. Dis. 2002, 2, 550-563.
4. Q. V. Sun, J. M. Xu, Y. B. Cao, W. N. Zhang, Q. Y. Wu, D. Z. Zhang, J. Zhang, H. Q. Zhao, Y. Y. Jiang, Eur. J. Med. Chem. 2007, 42, 1226-1233.
5. D. C. Lamb, B. C. Kelly, B. C. Baldwin, S. L. Kelly, Chem. Biol. Interact. 2000, 125, 165-175.
6. A. Robert, Clin. Microbiol. Rev. 1988, 1, 187-217.
7. S. Emami, M. Falahati, A. Banifatemi, K. Moshiri, A. Shafiee, Arch. Pharm. Pharm. Med. Chem. 2002, 7, 318-324.
8. J. Liu, L. Li, H. Dai, Z. Liu, J. Fang, J. Organometal. Chem. 2006, 691, 2686-2690.
9. W. Wang, C. Sheng, X. Che, H. Ji, Z. Miao, J. Yao, W. Zhang, Arch. Pharm. Chem. Life Sci. 2009, 342, 732-739.
10. Z. Rezaei, S. Khabnadideh, K. Pakshir, Z. Hossaini, F. Amiri, E. Assadpour, Eur. J. Med. Chem. 2009, 44, 3064-3067.
11. S. Khabnadideh, Z. Rezaei, A. Khalafi-Nezhad, K. Pakshir, A. Roosta, Z. Baratzadeh, Anti-Infect. Agents Med. Chem. 2008, 7, 215-218.
12. S. Khabnadideh, Z. Rezaei, A. Khalafi-nejad, K. Pakshir, M. J. Heiran, H. Shobeiri, Iranian J. Pharm. Sci. 2009, 5, 37-44.
13. Y. T. G. Liu, M. E. Ryan, H. M. Lee, L. M. J. Golub, Antimicrob. Agents Chemother. 2002, 46, 1455-1461.
14. T. Yashida, K. Jono, K. J. Okonoji, Antimicrob. Agents Chemother. 1997, 41, 1349-1351.
15. B. S. Patil, G. Krishnamurthy, H. S. BhojyaNaik, P. R. Latthe, M. Ghate, Eur. J. Med. Chem. 2010, 45, 3329-3334.
16. K. D. Thomas, A. V. Adhikari, N. S. Shetty, Eur. J. Med. Chem. 2010, 45, 3803-3810.