References
- Fridkin, S. K.; Jarvis, W. R. Clin. Microbiol. Rev. 1996, 9, 499.
- Farowski, F.; Vehreschild, J. J.; Cornely, O. A. Future Microbiol. 2007, 2(3), 231. https://doi.org/10.2217/17460913.2.3.231
- Aoyama, Y.; Yoshida, Y.; Sato, R. J. Biol. Chem. 1984, 259, 1661.
- Sun, Q.; Xu, J.; Cao, Y.; Zhang, W.; Wu, Q.; Zhang, D.; Zhang, J.; Zhao, H.; Jiang, Y. Eur. J. Med. Chem. 2007, 42, 1226. https://doi.org/10.1016/j.ejmech.2007.01.006
- Uchida, T.; Kagoshima, Y.; Konosu, T. Bioorg. Med. Chem. Lett. 2009, 19, 2013. https://doi.org/10.1016/j.bmcl.2009.02.036
- Na, Y-M.; Le Borgne, M.; Pagniez, F.; Le Baut, G.; Le Pape, P. Eur. J. Med. Chem. 2003, 38, 75. https://doi.org/10.1016/S0223-5234(02)00005-3
- Lebouvier, N.; Pagniez, F.; Duflos, M.; LePape, P.; Na, Y-M.; LeBaut, G.; LeBorgne, M. Bioorg. Med. Chem. Lett. 2007, 17, 3686. https://doi.org/10.1016/j.bmcl.2007.04.038
- Singh, I. P.; Sidhu, I.; Palak, B. U. S. Patent 6,1333,485, 2000.
- Konosu, T.; Miyaoka, T.; Tajima, Y.; Oida, S. Chem. Pharm. Bull. 1991, 39, 2241. https://doi.org/10.1248/cpb.39.2241
- Tasaka, A.; Tamura, N.; Matsushita, Y.; Kitazaki, T.; Hayashi, R.; Okonogi, K.; Itoh, K. Chem. Pharm. Bull. 1995, 43, 441. https://doi.org/10.1248/cpb.43.441
- Tasaka, A.; Tamura, N.; Matsushita, Y.; Teranishi, K.; Hayashi, R.; Okonogi, K.; Iroh, K. Chem. Pharm. Bull. 1993, 41, 1035. https://doi.org/10.1248/cpb.41.1035
- Galgiani, J.; Bartlett, M.; Ghannoum, M.; Espinel-Ingroff, A.; Lancaster, A.; Odds, F. NCCLS, 1995, 15, 129.
- Liao, R. S.; Robert, Rennie, P.; Talbot, J. A. Antimicrob. Agents Chemother. 2002, 46, 3236. https://doi.org/10.1128/AAC.46.10.3236-3242.2002
- Davey, K. G.; Szekely, A.; Johnson, E. M.; Warnock, D. W. Antimicrob. Agents Chemother. 1998, 42, 439. https://doi.org/10.1093/jac/42.4.439
- Mellado, E.; Garcia-Effron, G.; Alcazar-Fuoli, L.; Melchers, W. J. G.; Verweij, P. E.; Cuenca-Estrella, M.; Rodriguez-Tudela, J. L. Antimicrob. Agents Chemother. 2007, 51, 1897. https://doi.org/10.1128/AAC.01092-06
Cited by
- ChemInform Abstract: Synthesis and Activity of Novel 1-Halogenobenzylindole Linked Triazole Derivatives as Antifungal Agents. vol.42, pp.21, 2011, https://doi.org/10.1002/chin.201121160
- Antimicrobial evaluation, QSAR and docking studies of amide-linked 1,4-disubstituted 1,2,3-bistriazoles vol.24, pp.8, 2015, https://doi.org/10.1007/s00044-015-1378-9
- Chemoenzymatic Synthesis, Nanotization, and Anti-Aspergillus Activity of Optically Enriched Fluconazole Analogues vol.61, pp.8, 2017, https://doi.org/10.1128/AAC.00273-17
- Entry to Highly Hindered Chiral β-Amino Triazoles Bearing a gem-Diaryl Group by Azide-alkyne Click Chemistry vol.35, pp.6, 2011, https://doi.org/10.5012/bkcs.2014.35.6.1605
- Improved Laboratory Synthesis of YC-071, a Potent Azole Antifungal Agent vol.41, pp.4, 2011, https://doi.org/10.3184/174751917x14902201357419