Carbonic anhydrase inhibitors. The ß-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides

dc.contributor.author	Mastrolorenzo, Antonio
dc.contributor.author	GÜZEL, ÖZLEN
dc.contributor.author	Scozzafava, Andrea
dc.contributor.author	Mühlschlegel, Fritz A.
dc.contributor.author	Supuran, Claudiu T.
dc.contributor.author	Maresca, Alfonso
dc.contributor.author	Hall, Rebecca A.
dc.date.accessioned	2021-03-04T08:35:51Z
dc.date.available	2021-03-04T08:35:51Z
dc.identifier.citation	GÜZEL Ö., Maresca A., Hall R. A. , Scozzafava A., Mastrolorenzo A., Mühlschlegel F. A. , Supuran C. T. , "Carbonic anhydrase inhibitors. The ß-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, cilt.20, ss.2508-2511, 2010
dc.identifier.issn	0960-894X
dc.identifier.other	vv_1032021
dc.identifier.other	av_6412eca3-f0df-4873-b0f1-6c79021e6635
dc.identifier.uri	http://hdl.handle.net/20.500.12627/69651
dc.language.iso	eng
dc.subject	Kimya
dc.subject	Temel Bilimler (SCI)
dc.subject	Temel Bilimler
dc.title	Carbonic anhydrase inhibitors. The ß-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides
dc.type	Makale
dc.relation.journal	BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
dc.contributor.department	, ,
dc.identifier.volume	20
dc.identifier.startpage	2508
dc.identifier.endpage	2511
dc.contributor.firstauthorID	711478

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