O. Guezel Et Al. , "Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides," BIOORGANIC & MEDICINAL CHEMISTRY LETTERS , vol.20, no.8, pp.2508-2511, 2010
Guezel, O. Et Al. 2010. Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS , vol.20, no.8 , 2508-2511.
Guezel, O., Maresca, A., Hall, R. A., Scozzafava, A., Mastrolorenzo, A., Muehlschlegel, F. A., ... Supuran, C. T.(2010). Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS , vol.20, no.8, 2508-2511.
Guezel, Oezlen Et Al. "Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides," BIOORGANIC & MEDICINAL CHEMISTRY LETTERS , vol.20, no.8, 2508-2511, 2010
Guezel, Oezlen Et Al. "Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides." BIOORGANIC & MEDICINAL CHEMISTRY LETTERS , vol.20, no.8, pp.2508-2511, 2010
Guezel, O. Et Al. (2010) . "Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides." BIOORGANIC & MEDICINAL CHEMISTRY LETTERS , vol.20, no.8, pp.2508-2511.
@article{article, author={Oezlen Guezel Et Al. }, title={Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides}, journal={BIOORGANIC & MEDICINAL CHEMISTRY LETTERS}, year=2010, pages={2508-2511} }