about
Hyperchlorhidrosis caused by homozygous mutation in CA12, encoding carbonic anhydrase XIIStructure and inhibition of the CO2-sensing carbonic anhydrase Can2 from the pathogenic fungus Cryptococcus neoformansS-glycosyl primary sulfonamides--a new structural class for selective inhibition of cancer-associated carbonic anhydrasesIdentification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: synthesis, biological evaluation, and enzyme--ligand X-ray studiesBidentate Zinc Chelators for α-Carbonic Anhydrases that Produce a Trigonal Bipyramidal Coordination GeometryNatural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrasesStructural and inhibition insights into carbonic anhydrase CDCA1 from the marine diatom Thalassiosira weissflogiiSynthesis, structure-activity relationship studies, and X-ray crystallographic analysis of arylsulfonamides as potent carbonic anhydrase inhibitorsSulfocoumarins (1,2-benzoxathiine-2,2-dioxides): a class of potent and isoform-selective inhibitors of tumor-associated carbonic anhydrasesCombining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studiesCrystal structures of two tetrameric β-carbonic anhydrases from the filamentous ascomycete Sordaria macrosporaCyclic secondary sulfonamides: unusually good inhibitors of cancer-related carbonic anhydrase enzymesOut of the active site binding pocket for carbonic anhydrase inhibitorsCarbonic anhydrase inhibitors with dual-tail moieties to match the hydrophobic and hydrophilic halves of the carbonic anhydrase active siteStructure and inhibition studies of a type II beta-carbonic anhydrase psCA3 from Pseudomonas aeruginosaMapping Selective Inhibition of the Cancer-Related Carbonic Anhydrase IX Using Structure-Activity Relationships of Glucosyl-Based SulfamatesDiscovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV InhibitorsCrystal structure and kinetic studies of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium Vibrio choleraeAn Unusual Natural Product Primary Sulfonamide: Synthesis, Carbonic Anhydrase Inhibition, and Protein X-ray Structures of Psammaplin CKinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitorsBenzoxaborole as a new chemotype for carbonic anhydrase inhibitionDiscovery of a new family of carbonic anhydrases in the malaria pathogen Plasmodium falciparum--the η-carbonic anhydrases
P50
Q24304931-956CD62C-92ED-45B3-8C10-39477F3F5E6AQ27653101-5211BE1A-5449-45A7-A7EB-63C4BF99A045Q27657780-401B2090-D78C-42D4-8431-8B6882CBD027Q27659940-85469632-9EE3-4AD4-B521-FA3357D90502Q27663412-548B0EFF-810F-47E1-A328-B2BB4F950AA3Q27666744-F0C7ADC1-398E-421B-93E8-71072FF5F866Q27677550-0CA220D6-A264-4C5D-A17E-3748AF286756Q27678178-8FE3692D-F7E6-4B4B-8B51-ACE900D62DF1Q27683603-CB210966-C106-4636-8288-D243E5D4BCFAQ27687793-2A45380E-154D-4985-98F3-89159FA01EAFQ27689058-E89DA8C2-0682-4CC6-B1F7-C5BF7F673931Q27689678-C0BC3023-B469-418D-B253-76ADA24DD0CEQ27696192-0F355804-008C-446D-AD79-CBAE5CE96B12Q27697330-D68DAF2C-891E-47B3-9927-6CBC621DC9A9Q27701002-59B3BBBC-172F-49DC-801F-C60EE0A82B2DQ27701610-BA0D1599-45ED-4A42-A19C-CAF18954FF85Q27702516-3494CEC6-843D-488E-AD8F-4631FB942662Q27702913-2828A94B-D891-4F20-8D68-9AA2B289A59AQ27704855-29C760B1-33FF-40FE-9A16-ABEC266348DBQ27711525-BF365544-0470-4313-B69B-62E384712FA1Q27728279-2B0ACDEA-41F1-4167-9EB1-7170EE52BA83Q27973368-32079A3F-CF9D-46A6-85EF-E72B62081F71
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Daniela Vullo
@ast
Daniela Vullo
@en
Daniela Vullo
@es
Daniela Vullo
@nl
Daniela Vullo
@sl
type
label
Daniela Vullo
@ast
Daniela Vullo
@en
Daniela Vullo
@es
Daniela Vullo
@nl
Daniela Vullo
@sl
prefLabel
Daniela Vullo
@ast
Daniela Vullo
@en
Daniela Vullo
@es
Daniela Vullo
@nl
Daniela Vullo
@sl