Supplemental material
Open access
1,802
Views
40
CrossRef citations to date
0
Altmetric
Research Article
Microwave-assisted synthesis and bioevaluation of new sulfonamides
Halise Inci GulDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey; Correspondence[email protected]
, Cem YamaliDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey;
http://orcid.org/0000-0002-4833-7900
Fatma YesilyurtDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey;
, Hiroshi SakagamiDivision of Pharmacology, Meikai University School of Dentistry, Sakado, Saitama, Japan;
, Kaan KucukogluDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey;
, Ilhami GulcinDepartment of Chemistry, Faculty of Science, Ataturk University, Erzurum, Turkey; ;Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia;
http://orcid.org/0000-0001-5993-1668
Mustafa GulDepartment of Physiology, Faculty of Medicine, Ataturk University, Erzurum, Turkey;
& Claudiu T. SupuranNeurofarba Departmente Laboratorio di Chimica Bioinorganica, Universita degli Studi di Firenze, Sesto Fiorentino, Florence, Italy
show all
Pages 369-374
|
Received 11 Aug 2016, Accepted 25 Oct 2016, Published online: 06 Mar 2017
Related Research Data
Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.
Source:
American Chemical Society (ACS)
Synthesis of 6-aryl-substituted sulfocoumarins and investigation of their carbonic anhydrase inhibitory action.
Source:
Elsevier BV
Structure and function of carbonic anhydrases
Source:
Portland Press Ltd.
Synthesis and Antifungal Activity of 2-Pyrazolines
Source:
Wiley
Overcoming physiologic barriers to cancer treatment by molecularly targeting the tumor microenvironment.
Source:
American Association for Cancer Research (AACR)
Synthesis of chalcone-imide derivatives and investigation of their anticancer and antimicrobial activities, carbonic anhydrase and acetylcholinesterase enzymes inhibition profiles.
Source:
Taylor & Francis
Novel sulphonamides incorporating triazene moieties show powerful carbonic anhydrase I and II inhibitory properties.
Source:
Taylor & Francis Group
Towards development of selective and reversible pyrazoline based MAO-inhibitors: Synthesis, biological evaluation and docking studies.
Source:
Elsevier BV
Activation studies of the α- and β-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae with amines and amino acids.
Source:
Informa UK Limited
Multidrug resistance reverting activity and antitumor profile of new phenothiazine derivatives
Source:
Elsevier BV
Synthesis of mono Mannich bases of 2-(4-hydroxybenzylidene)-2,3-dihydroinden-1-one and evaluation of their cytotoxicities
Source:
Informa UK Limited
Carbonic anhydrases: novel therapeutic applications for inhibitors and activators
Source:
Springer Science and Business Media LLC
Effects of 3-styrylchromones on metabolic profiles and cell death in oral squamous cell carcinoma cells
Source:
The Authors. Published by Elsevier Inc.
Synthesis and antiinflammatory activity of some new 1,3,5-trisubstituted pyrazolines bearing benzene sulfonamide.
Source:
Elsevier BV
Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides.
Source:
Informa UK Limited
Synthesis and structure elucidation of 1-(2,5/3,5-difluorophenyl)-3-(2,3/2,4/2,5/3,4-dimethoxyphenyl)-2-propen-1-ones as anticancer agents
Source:
Springer Science and Business Media LLC
Cytotoxicity, apoptosis, and QSAR studies of phenothiazine derived methoxylated chalcones as anticancer drug candidates
Source:
Springer Science and Business Media LLC
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
Source:
Elsevier BV
Design and synthesis of some new pyrazolyl-pyrazolines as potential anti-inflammatory, analgesic and antibacterial agents.
Source:
Elsevier BV
New selective carbonic anhydrase IX inhibitors: Synthesis and pharmacological evaluation of diarylpyrazole-benzenesulfonamides
Source:
HAL CCSD
Synthesis and evaluation of some new pyrazoline substituted benzenesulfonylureas as potential antiproliferative agents.
Source:
Elsevier BV
Carbonic Anhydrase Inhibitors
Source:
Wiley
Synthesis and bioactivity studies on new 4-(3-(4-Substitutedphenyl)-3a,4-dihydro-3H-indeno[1,2-c]pyrazol-2-yl) benzenesulfonamides.
Source:
Informa
Synthesis of novel sulfamides incorporating phenethylamines and determination of their inhibition profiles against some metabolic enzymes
Source:
WILEY-V C H VERLAG GMBH
Inhibitory effects of some drugs on carbonic anhydrase enzyme purified from Kangal Akkaraman sheep in Sivas, Turkey
Source:
Wiley
Synthesis and bioactivity studies of 1-aryl-3-(2-hydroxyethylthio)-1-propanones
Source:
Informa UK Limited
Synthesis, cytotoxicities, and carbonic anhydrase inhibition potential of 6-(3-aryl-2-propenoyl)-2(3H)-benzoxazolones
Source:
Informa UK Limited
The Determination of Enzyme Dissociation Constants
Source:
American Chemical Society (ACS)
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.