A class of sulfonamide carbonic anhydrase inhibitors with neuropathic pain modulating effects
about
Non-Classical Inhibition of Carbonic AnhydraseThe anticonvulsant sulfamide JNJ-26990990 and its S,S-dioxide analog strongly inhibit carbonic anhydrases: solution and X-ray crystallographic studiesA class of carbonic anhydrase I - selective activators.How many carbonic anhydrase inhibition mechanisms exist?Novel Sulfamide-Containing Compounds as Selective Carbonic Anhydrase I Inhibitors.Drug interaction considerations in the therapeutic use of carbonic anhydrase inhibitors.Carbonic anhydrase inhibition and the management of neuropathic pain.Advances in structure-based drug discovery of carbonic anhydrase inhibitors.Investigation of piperazines as human carbonic anhydrase I, II, IV and VII activators.Psychoactive substances belonging to the amphetamine class potently activate brain carbonic anhydrase isoforms VA, VB, VII, and XII.Synthesis and biological evaluation of histamine Schiff bases as carbonic anhydrase I, II, IV, VII, and IX activators.Synthesis and carbonic anhydrase I, II, VII, and IX inhibition studies with a series of benzo[d]thiazole-5- and 6-sulfonamides.Novel 6- and 7-Substituted Coumarins with Inhibitory Action against Lipoxygenase and Tumor-Associated Carbonic Anhydrase IX.Special Issue: Sulfonamides.Synthesis, molecular modeling, and biological evaluation of 4-[5-aryl-3-(thiophen-2-yl)-4,5-dihydro-1H-pyrazol-1-yl] benzenesulfonamides toward acetylcholinesterase, carbonic anhydrase I and II enzymes.Potent and Selective Carboxylic Acid Inhibitors of Tumor-Associated Carbonic Anhydrases IX and XII.Crystal structure of the human carbonic anhydrase II adduct with 1-(4-sulfamoylphenyl-ethyl)-2,4,6-triphenylpyridinium perchlorate, a membrane-impermeant, isoform selective inhibitor.Lucky Switcheroo: Dramatic Potency and Selectivity Improvement of Imidazoline Inhibitors of Human Carbonic Anhydrase VII.Carbonic anhydrase inhibition for the management of cerebral ischemia: in vivo evaluation of sulfonamide and coumarin inhibitors.Inhibition studies of Brucella suis β-carbonic anhydrases with a series of 4-substituted pyridine-3-sulphonamides.A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents.
P2860
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P2860
A class of sulfonamide carbonic anhydrase inhibitors with neuropathic pain modulating effects
description
2015 nî lūn-bûn
@nan
2015 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
A class of sulfonamide carboni ...... pathic pain modulating effects
@ast
A class of sulfonamide carboni ...... pathic pain modulating effects
@en
A class of sulfonamide carboni ...... pathic pain modulating effects
@nl
type
label
A class of sulfonamide carboni ...... pathic pain modulating effects
@ast
A class of sulfonamide carboni ...... pathic pain modulating effects
@en
A class of sulfonamide carboni ...... pathic pain modulating effects
@nl
prefLabel
A class of sulfonamide carboni ...... pathic pain modulating effects
@ast
A class of sulfonamide carboni ...... pathic pain modulating effects
@en
A class of sulfonamide carboni ...... pathic pain modulating effects
@nl
P50
P3181
P1476
A class of sulfonamide carboni ...... pathic pain modulating effects
@en
P2093
Melissa Pinard
P304
P3181
P356
10.1016/J.BMC.2015.02.027
P407
P50
P577
2015-04-15T00:00:00Z