Related references
Note: Only part of the references are listed.How many carbonic anhydrase inhibition mechanisms exist?
Claudiu T. Supuran
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY (2016)
Rational Design, Synthesis, and Preliminary Structure-Activity Relationships of α-Substituted-2-Phenylcyclopropane Carboxylic Acids as Inhibitors of Salmonella typhimurium O-Acetylserine Sulfhydrylase
Marco Pieroni et al.
JOURNAL OF MEDICINAL CHEMISTRY (2016)
Hit Recycling: Discovery of a Potent Carbonic Anhydrase Inhibitor by in Silico Target Fishing
Mattia Mori et al.
ACS CHEMICAL BIOLOGY (2015)
The zinc coordination pattern in the η-carbonic anhydrase from Plasmodium falciparum is different from all other carbonic anhydrase genetic families
Giuseppina De Simone et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2015)
Drug repositioning and repurposing: terminology and definitions in literature
Joris Langedijk et al.
DRUG DISCOVERY TODAY (2015)
Target-Based Drug Repositioning Using Large-Scale Chemical-Protein Interactome Data
Ryusuke Sawada et al.
JOURNAL OF CHEMICAL INFORMATION AND MODELING (2015)
Discovery of Multitarget Antivirals Acting on Both the Dengue Virus NS5-NS3 Interaction and the Host Src/Fyn Kinases
Paolo Vincetti et al.
JOURNAL OF MEDICINAL CHEMISTRY (2015)
Rational Design and Synthesis of Thioridazine Analogues as Enhancers of the Antituberculosis Therapy
Marco Pieroni et al.
JOURNAL OF MEDICINAL CHEMISTRY (2015)
An Experimental and Computational Approach to Understanding the Reactions of Acyl Nitroso Compounds in [4+2] Cycloadditions
Duangduan Chaiyaveij et al.
JOURNAL OF ORGANIC CHEMISTRY (2015)
Repurposing of the Open Access Malaria Box for Kinetoplastid Diseases Identifies Novel Active Scaffolds against Trypanosomatids
Marcel Kaiser et al.
JOURNAL OF BIOMOLECULAR SCREENING (2015)
Discovery of a new family of carbonic anhydrases in the malaria pathogen Plasmodium falciparum-The η-carbonic anhydrases
Sonia Del Prete et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2014)
Design, synthesis and investigation on the structure-activity relationships of N-substituted 2-aminothiazole derivatives as antitubercular agents
Marco Pieroni et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2014)
Exploring the Influence of the Protein Environment on Metal-Binding Pharmacophores
David P. Martin et al.
JOURNAL OF MEDICINAL CHEMISTRY (2014)
The alpha-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 is highly susceptible to inhibition by sulfonamides
Daniela Vullo et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2013)
In silico drug repositioning - what we need to know
Zhichao Liu et al.
DRUG DISCOVERY TODAY (2013)
Anti-infective carbonic anhydrase inhibitors: a patent and literature review
Clemente Capasso et al.
EXPERT OPINION ON THERAPEUTIC PATENTS (2013)
Dihalogenated sulfanilamides and benzolamides are effective inhibitors of the three β-class carbonic anhydrases from Mycobacterium tuberculosis
Alfonso Maresca et al.
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY (2013)
Inhibition of the β-class carbonic anhydrases from Mycobacterium tuberculosis with carboxylic acids
Alfonso Maresca et al.
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY (2013)
2-Aminonicotinic Acid 1-Oxides Are Chemically Stable Inhibitors of Quinolinic Acid Synthesis in the Mammalian Brain: A Step toward New Antiexcitotoxic Agents
Gian Paolo Vallerini et al.
JOURNAL OF MEDICINAL CHEMISTRY (2013)
Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?
Vincenzo Alterio et al.
CHEMICAL REVIEWS (2012)
Design and synthesis of trans-2-substituted-cyclopropane-1-carboxylic acids as the first non-natural small molecule inhibitors of O-acetylserine sulfhydrylase
Laura Amori et al.
MEDCHEMCOMM (2012)
Targeting Tumor Hypoxia: Suppression of Breast Tumor Growth and Metastasis by Novel Carbonic Anhydrase IX Inhibitors
Yuanmei Lou et al.
CANCER RESEARCH (2011)
Build-Up Algorithm for Atomic Correspondence between Chemical Structures
Takeshi Kawabata
JOURNAL OF CHEMICAL INFORMATION AND MODELING (2011)
Drug repurposing and adverse event prediction using high-throughput literature analysis
Spyros N. Deftereos et al.
WILEY INTERDISCIPLINARY REVIEWS-SYSTEMS BIOLOGY AND MEDICINE (2011)
Bacterial carbonic anhydrases as drug targets: toward novel antibiotics?
Claudiu T. Supuran
FRONTIERS IN PHARMACOLOGY (2011)
Bidentate Zinc Chelators for α-Carbonic Anhydrases that Produce a Trigonal Bipyramidal Coordination Geometry
Johannes Schulze Wischeler et al.
CHEMMEDCHEM (2010)
Polyamines Inhibit Carbonic Anhydrases by Anchoring to the Zinc-Coordinated Water Molecule
Fabrizio Carta et al.
JOURNAL OF MEDICINAL CHEMISTRY (2010)
Selective 5-Hydroxytryptamine 2C Receptor Agonists Derived from the Lead Compound Tranylcypromine: Identification of Drugs with Antidepressant-Like Action
Sung Jin Cho et al.
JOURNAL OF MEDICINAL CHEMISTRY (2009)
Carbonic anhydrase inhibitors:: Inhibition of Plasmodium falciparum carbonic anhydrase with aromatic/heterocyclic sulfonamides-in vitro and in vivo studies
Jerapan Krungkrai et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2008)
Carbonic anhydrases: novel therapeutic applications for inhibitors and activators
Claudiu T. Supuran
NATURE REVIEWS DRUG DISCOVERY (2008)
Direct screening of natural product extracts using mass spectrometry
Hoan Vu et al.
JOURNAL OF BIOMOLECULAR SCREENING (2008)
Carbonic anhydrase inhibitors.: Inhibition of Plasmodium falciparum carbonic anhydrase with aromatic sulfonamides:: towards antimalarials with a novel mechanism of action?
J Krungkrai et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2005)
Drug repositioning: Identifying and developing new uses for existing drugs
TT Ashburn et al.
NATURE REVIEWS DRUG DISCOVERY (2004)
Maximum common subgraph isomorphism algorithms for the matching of chemical structures
JW Raymond et al.
JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN (2002)
Share Paper
