(Q58863339)

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Carbonic anhydrase activators: amino acyl/dipeptidyl histamine derivatives bind with high affinity to isozymes I, II and IV and act as efficient activators

scientific article published on 01 December 1999

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10658596%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Carbonic anhydrase activators: amino acyl/dipeptidyl histamine derivatives bind with high affinity to isozymes I, II and IV and act as efficient activators (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10658596%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Andrea Scozzafava

2

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3 November 2019

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C T Supuran

1

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3 November 2019

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1 December 1999

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3 November 2019

Bioorganic & Medicinal Chemistry

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3 November 2019

7

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3 November 2019

12

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3 November 2019

2915-2923

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3 November 2019

Carbonic anhydrase inhibitors — Part 53. Synthesis of substituted-pyridinium derivatives of aromatic sulfonamides: The first non-polymeric membrane-impermeable inhibitors with selectivity for isozyme IV

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Novel aromatic/heterocyclic sulfonamides and their metal complexes as inhibitors of carbonic anhydrase isozymes I, II and IV.

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Carbonic anhydrase activators: X-ray crystallographic and spectroscopic investigations for the interaction of isozymes I and II with histamine

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Carbonic anhydrase activators. 3: structure-activity correlations for a series of isozyme II activators.

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Carbonic anhydrase activators. VII. Isozyme II activation by bisazolyl-methanes, -ethanes and related azoles

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Carbonic anhydrase activators. XV. A kinetic study of the interaction of bovine isozyme II with pyrazoles, bis- and tris-azolyl-methanes

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Carbonic anhydrase activators. Part 17. Synthesis and activation study of a series of 1-(1,2,4-triazole-(1H)-3-yl)-2,4,6-trisubstituted-pyridinium salts against isozymes I, II and IV

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Identification of two hydrophobic patches in the active-site cavity of human carbonic anhydrase II by solution-phase and solid-state studies and their use in the development of tight-binding inhibitors

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Secondary Interactions Significantly Removed from the Sulfonamide Binding Pocket of Carbonic Anhydrase II Influence Inhibitor Binding Constants

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Carbonic anhydrase inhibitors — Part 29 1: Interaction of isozymes I, II and IV with benzolamide-like derivatives

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Carbonic Anhydrase Inhibitors. Synthesis of Water-Soluble, Topically Effective, Intraocular Pressure-Lowering Aromatic/Heterocyclic Sulfonamides Containing Cationic or Anionic Moieties: Is the Tail More Important than the Ring?1

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Novel H3 receptor antagonists. Sulfonamide homologs of histamine

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Carbonic Anhydrase Inhibitors: Synthesis of Water-Soluble, Aminoacyl/Dipeptidyl Sulfonamides Possessing Long-Lasting Intraocular Pressure-Lowering Properties via the Topical Route1

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Screening derivatized peptide libraries for tight binding inhibitors to carbonic anhydrase II by electrospray ionization-mass spectrometry

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Advances in the Chemistry of Carbodiimides

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Structural and functional differences between carbonic anhydrase isoenzymes I and II as studied by site-directed mutagenesis

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Carbon-13 nuclear magnetic resonance probe of active-site ionizations in human carbonic anhydrase B

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The Catalytic Versatility of Erythrocyte Carbonic Anhydrase. III. Kinetic Studies of the Enzyme-Catalyzed Hydrolysis of p-Nitrophenyl Acetate*

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Catalysis and inhibition of human carbonic anhydrase IV.

1 reference

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Identifiers

10.1016/S0968-0896(99)00227-8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10658596%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10658596%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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