Supplemental material
Open access
1,316
Views
9
CrossRef citations to date
0
Altmetric
Research Article
Synthesis, characterization and in vitro inhibition of metal complexes of pyrazole based sulfonamide on human erythrocyte carbonic anhydrase isozymes I and II
Nurgün BüyükkıdanDepartment of Chemistry, Arts and Science Faculty, Dumlupinar University, Kutahya, TurkeyCorrespondence[email protected]
View further author information
, View further author information
Bülent BüyükkıdanDepartment of Chemistry, Arts and Science Faculty, Dumlupinar University, Kutahya, TurkeyView further author information
, Metin BülbülDepartment of Chemistry, Arts and Science Faculty, Dumlupinar University, Kutahya, TurkeyView further author information
, Rahmi KasımoğullarıDepartment of Chemistry, Arts and Science Faculty, Dumlupinar University, Kutahya, TurkeyView further author information
& Samet MertDepartment of Chemistry, Arts and Science Faculty, Dumlupinar University, Kutahya, TurkeyView further author information
Pages 208-213
|
Received 26 Jun 2016, Accepted 04 Oct 2016, Published online: 23 Jan 2017
Related Research Data
Human mitochondrial carbonic anhydrase VB. cDNA cloning, mRNA expression, subcellular localization, and mapping to chromosome x.
Source:
Elsevier BV
The Structure ofN-phenyl-pyrazoles and Indazoles: Mononitro, Dinitro, and Trinitro Derivatives
Source:
Wiley
Synthesis, characterization and crystal structures of a bidentate indazole–thiazine derivative ligand and its cobalt (II) and cadmium (II) metal complexes
Source:
Elsevier BV
Carbonic Anhydrase Inhibitors. Part 461 Inhibition of Carbonic Anhydrase Isozymes I, II and IV With Trifluoromethylsulfonamide Derivatives and Their Zinc(II) and Copper(II) Complexes
Source:
Hindawi Limited
1,3,4-Thiadiazole- and Thiadiazolinesulfonamides as Carbonic Anhydrase Inhibitors. Synthesis and Structural Studies
Source:
American Chemical Society (ACS)
(3,4-Dihydroxyphenyl)(2,3,4-trihydroxyphenyl)methanone and its derivatives as carbonic anhydrase isoenzymes inhibitors
Source:
Taylor & Francis Ltd
Human carbonic anhydrase XII: cDNA cloning, expression, and chromosomal localization of a carbonic anhydrase gene that is overexpressed in some renal cell cancers
Source:
Proceedings of the National Academy of Sciences
Biological Activity of Diphenylmethanone Derivatives
Source:
Wiley
Complexes With Biologically Active Ligands. Part 101 Inhibition of Carbonic Anhydrase Isozymes I and II With Metal Complexes of Imidazo[2,1−b]-1,3,4-Thiadiazole-2-Sulfonamide
Source:
Hindawi Limited
Oxidation of cyanobenzocycloheptatrienes: Synthesis, photooxygenation reaction and carbonic anhydrase isoenzymes inhibition properties of some new benzotropone derivatives.
Source:
PERGAMON-ELSEVIER SCIENCE LTD
Structure and mechanism of carbonic anhydrase.
Source:
Elsevier BV
Cobalt(II) complexes of the antibiotic sulfadiazine, the X-ray single crystal structure of [Co(C10H9N4O2S)2(CH3OH)2]
Source:
Elsevier BV
Notes - Heterocyclic Sulfonamides as Carbonic Anhydrase Inhibitors. 2-Acylamido- and 2-Sulfonamido-1,3,4-thiadiazole-5-sulfonamides
Source:
American Chemical Society (ACS)
Synthesis and carbonic anhydrase inhibitory properties of sulfamides structurally related to dopamine.
Source:
Elsevier BV
COMPLEXES WITH BIOLOGICALLY ACTIVE LIGANDS. Part 5. Zn(ll) AND Cd(ll) COORDINATION COMPOUNDS OF HYDRAZINE AND HETEROCYCLIC SULFONAMIDES AS INHIBITORS OF THE ZINC ENZYME CARBONIC ANHYDRASE
Source:
Walter de Gruyter GmbH
Complexes With Biologically Active Ligands. Part 6 Ni(II) Coordination Compounds of Hydrazine and Heterocyclic Sulfonamides as Inhibitors of the Zinc Enzyme Carbonic Anhydrase.
Source:
Hindawi Limited
Synthesis and carbonic anhydrase isoenzymes I and II inhibitory effects of novel benzylamine derivatives.
Source:
Taylor & Francis Ltd
Heterocyclic Sulfonamides as Carbonic Anhydrase Inhibitors1
Source:
American Chemical Society (ACS)
Review The Preclinical Pharmacology of Dorzolamide Hydrochloride, a Topical Carbonic Anhydrase Inhibitor
Source:
Mary Ann Liebert Inc
Determination of sepharose-bound protein with coomassie brilliant blue G-250
Source:
Elsevier BV
Development and pharmacological characterization of a modified procedure for the measurement of carbonic anhydrase activity
Source:
Elsevier BV
Human carbonic anhydrase XIV (CA14): cDNA cloning, mRNA expression, and mapping to chromosome 1.
Source:
Elsevier BV
Kinetic Properties of Carbonic Anhydrase Purified from Gills of Rainbow Trout (Oncorhynchus mykiss)
Source:
Informa UK Limited
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Source:
Springer Science and Business Media LLC
The Preparation of Heterocyclic Sulfonamides1
Source:
American Chemical Society (ACS)
In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II
Source:
Elsevier BV
Carbonic anhydrase inhibitors: Synthesis and inhibitory properties of 1,3,4-thiadiazole-2,5-bissulfonamide
Source:
Elsevier BV
Synthesis, Electrochemistry and Spectral Studies on Cobalt(II) and Manganese (II) Complexes with 12-,14-,15-, and 18-membered N4, N2O2, N2O2S, N6 Donor Macrocyclic Ligands
Source:
Informa UK Limited
Inhibition of the Archaeal β-Class (Cab) and γ-Class (Cam) Carbonic Anhydrases
Source:
Bentham Science Publishers Ltd.
3D hydrogen bonded heteronuclear CoII, NiII, CuII and ZnII aqua complexes derived from dipicolinic acid
Source:
Elsevier BV
Effects of low molecular weight plasma inhibitors of rainbow trout (Oncorhynchus mykiss) on human erythrocyte carbonic anhydrase-II isozyme activity in vitro and rat erythrocytes in vivo
Source:
Informa UK Limited
Related research
People also read lists articles that other readers of this article have read.
Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.
Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.