Recent advances in the discovery of zinc-binding motifs for the development of carbonic anhydrase inhibitors.
about
A class of carbonic anhydrase I - selective activators.Designing carbonic anhydrase inhibitors for the treatment of breast cancer.Bacterial, fungal and protozoan carbonic anhydrases as drug targets.How many carbonic anhydrase inhibition mechanisms exist?Synthesis and bioactivity studies of 1-aryl-3-(2-hydroxyethylthio)-1-propanones.In Vivo Evaluation of Selective Carbonic Anhydrase Inhibitors as Potential Anticonvulsant Agents.Hydroxylamine-O-sulfonamide is a versatile lead compound for the development of carbonic anhydrase inhibitors.Carbonic Anhydrase Glycoinhibitors belonging to the Aminoxysulfonamide Series.A failed tentative to design a super carbonic anhydrase having the biochemical properties of the most thermostable CA (SspCA) and the fastest (SazCA) enzymes.Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors.Synthesis and carbonic anhydrase I, II, VII, and IX inhibition studies with a series of benzo[d]thiazole-5- and 6-sulfonamides.Effective Access to Multivalent Inhibitors of Carbonic Anhydrases Promoted by Peptide Bioconjugation.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.Benzoxaboroles as Efficient Inhibitors of the β-Carbonic Anhydrases from Pathogenic Fungi: Activity and Modeling Study.Carbonic anhydrase I, II, IV and IX inhibition with a series of 7-amino-3,4-dihydroquinolin-2(1H)-one derivatives.Synthesis of an acridine orange sulfonamide derivative with potent carbonic anhydrase IX inhibitory action.Sulphonamide inhibition studies of the β-carbonic anhydrase from the bacterial pathogen Clostridium perfringens.
P2860
Q31140231-D4A21FA5-5924-4B37-A3D6-39F1DA1BBD2DQ38428521-41773E01-DF9B-46ED-BF8D-162BBF48F2F5Q38559435-57D8C925-386A-47A0-A046-5BB62D2A90E5Q38653464-508A12A3-42EB-412E-A592-8E17A5E4C423Q38756920-455960B1-DA23-469E-99BB-272DB1A908FDQ38903347-22DF3ABA-D966-45F5-A2E4-A21269D40ACCQ40815863-1DC3BA15-4A07-48B3-935B-D253571FAF16Q41108486-6A043DE5-6D5C-4BB0-93DE-0DC136AEE7E4Q41434488-B5B87BD7-8E57-4595-A570-A3F3FA05BA8EQ47719833-B03FC2D0-AC1B-4BE7-98A7-503AA02FA677Q48017394-D7D7BE08-F7E9-4AE3-9197-1EFABE31D51CQ48208568-3EFE1314-467C-4B4F-9D70-A22248B09FE4Q48293922-F1DFB501-7561-4500-8136-61BAD13755A8Q49897501-4FCB0942-F97F-4B9A-97DD-85E12766B324Q50927587-FB5D17AC-2C14-45CC-B3EC-A04B77864CEAQ51089283-212C9852-0195-4412-A2F7-83CF6FD9DFB7Q52816899-F96A0250-B668-4793-BCCC-3A611FFB107A
P2860
Recent advances in the discovery of zinc-binding motifs for the development of carbonic anhydrase inhibitors.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh
2014年學術文章
@zh-hant
name
Recent advances in the discove ...... carbonic anhydrase inhibitors.
@en
type
label
Recent advances in the discove ...... carbonic anhydrase inhibitors.
@en
prefLabel
Recent advances in the discove ...... carbonic anhydrase inhibitors.
@en
P2860
P1476
Recent advances in the discove ...... carbonic anhydrase inhibitors
@en
P2093
Claudiu T Supuran
P2860
P304
P356
10.3109/14756366.2014.913587
P577
2014-06-18T00:00:00Z