Discovery of New Potential Anti-Infective Compounds Based on Carbonic Anhydrase Inhibitors by Rational Target-Focused Repurposing Approaches. (Q36053050)

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English	Discovery of New Potential Anti-Infective Compounds Based on Carbonic Anhydrase Inhibitors by Rational Target-Focused Repurposing Approaches.	scientific article

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14 March 2020

Discovery of New Potential Anti-Infective Compounds Based on Carbonic Anhydrase Inhibitors by Rational Target-Focused Repurposing Approaches (English)

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14 March 2020

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14 March 2020

Clemente Capasso

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14 March 2020

Claudiu T Supuran

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Claudiu T Supuran

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Giannamaria Annunziato

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Giannamaria Annunziato

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Marco Pieroni

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Gabriele Costantino

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Gabriele Costantino

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Viviana De Luca

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Viviana De Luca

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Daniela Vullo

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Francesca D'Alba

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14 March 2020

Agostino Bruno

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publication date

15 June 2016

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1904-1914

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14 March 2020

Drug repositioning and repurposing: terminology and definitions in literature

1 reference

https://api.crossref.org/works/10.1002%2FCMDC.201600180

21 January 2018

Hit Recycling: Discovery of a Potent Carbonic Anhydrase Inhibitor by in Silico Target Fishing.

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Repurposing of the Open Access Malaria Box for Kinetoplastid Diseases Identifies Novel Active Scaffolds against Trypanosomatids

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Target-Based Drug Repositioning Using Large-Scale Chemical-Protein Interactome Data

1 reference

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Drug repurposing and adverse event prediction using high-throughput literature analysis

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In silico drug repositioning: what we need to know

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Maximum common subgraph isomorphism algorithms for the matching of chemical structures

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Build-up algorithm for atomic correspondence between chemical structures

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Ligand efficiency indices as guideposts for drug discovery.

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Design and synthesis of trans-2-substituted-cyclopropane-1-carboxylic acids as the first non-natural small molecule inhibitors of O-acetylserine sulfhydrylase

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Rational Design, Synthesis, and Preliminary Structure-Activity Relationships of α-Substituted-2-Phenylcyclopropane Carboxylic Acids as Inhibitors of Salmonella typhimurium O-Acetylserine Sulfhydrylase.

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2-Aminonicotinic acid 1-oxides are chemically stable inhibitors of quinolinic acid synthesis in the mammalian brain: a step toward new antiexcitotoxic agents.

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Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

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Bacterial carbonic anhydrases as drug targets: toward novel antibiotics?

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Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms?

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Anti-infective carbonic anhydrase inhibitors: a patent and literature review

1 reference

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How many carbonic anhydrase inhibition mechanisms exist?

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Exploring the influence of the protein environment on metal-binding pharmacophores

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Bidentate Zinc Chelators for α-Carbonic Anhydrases that Produce a Trigonal Bipyramidal Coordination Geometry

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Direct screening of natural product extracts using mass spectrometry.

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Targeting tumor hypoxia: suppression of breast tumor growth and metastasis by novel carbonic anhydrase IX inhibitors.

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Polyamines inhibit carbonic anhydrases by anchoring to the zinc-coordinated water molecule

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Carbonic anhydrase inhibitors: inhibition of Plasmodium falciparum carbonic anhydrase with aromatic/heterocyclic sulfonamides-in vitro and in vivo studies

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Carbonic anhydrase inhibitors. Inhibition of Plasmodium falciparum carbonic anhydrase with aromatic sulfonamides: towards antimalarials with a novel mechanism of action?

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Discovery of a new family of carbonic anhydrases in the malaria pathogen Plasmodium falciparum--the η-carbonic anhydrases

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The zinc coordination pattern in the η-carbonic anhydrase from Plasmodium falciparum is different from all other carbonic anhydrase genetic families

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An Experimental and Computational Approach to Understanding the Reactions of Acyl Nitroso Compounds in [4 + 2] Cycloadditions

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Drug Repurposing from an Academic Perspective

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Inhibition of the β-class carbonic anhydrases from Mycobacterium tuberculosis with carboxylic acids

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The alpha-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 is highly susceptible to inhibition by sulfonamides

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10.1002/CMDC.201600180

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14 March 2020

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Europe PubMed Central

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14 March 2020

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