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Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Treatment of Chronic Macular Edema With Acetazolamide

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Zonisamide for Weight Loss in Obese Adults

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Saccharin Inhibits Carbonic Anhydrases: Possible Explanation for its Unpleasant Metallic Aftertaste

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Carbonic Anhydrase Activators. Activation of Isozymes I, II, IV, VA, VII, and XIV with L ‐ and D ‐Histidine and Crystallographic Analysis of Their Adducts with Isoform II: Engineering Proton‐Transfer Processes within the Active Site of an Enzyme

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Carbonic Anhydrase Inhibitors: The First Selective, Membrane‐Impermeant Inhibitors Targeting the Tumor‐Associated Isozyme IX.

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HIF‐1α and CA IX staining in invasive breast carcinomas: Prognosis and treatment outcome

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Carbonic Anhydrase Activators. 3: Structure-Activity Correlations for a Series of Isozyme I1 Activators

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Carbonic anhydrase inhibitors

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Activation of carbonic anhydrase isozymes

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X-ray crystallographic studies of mammalian carbonic anhydrase isozymes

inferredcites →https://doi.org/10.1007/s10555-007-9058-yopenalex-snapshot

Hypoxia and cancer

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Regulation of tumor pH and the role of carbonic anhydrase 9

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

inferredcites →https://doi.org/10.1016/j.bmc.2007.03.004openalex-snapshot

Carbonic anhydrase activators: The first activation study of the human secretory isoform VI with amino acids and amines

inferredcites →https://doi.org/10.1016/j.bmc.2007.08.037openalex-snapshot

Carbonic anhydrase inhibitors: Cloning, characterization, and inhibition studies of the cytosolic isozyme III with sulfonamides

inferredcites →https://doi.org/10.1016/j.bmcl.2003.09.062openalex-snapshot

Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX

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Carbonic anhydrase inhibitors: N-(p-sulfamoylphenyl)-α-d-glycopyranosylamines as topically acting antiglaucoma agents in hypertensive rabbits

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Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with EMATE, a dual inhibitor of carbonic anhydrases and steroid sulfatase

inferredcites →https://doi.org/10.1016/j.bmcl.2003.11.014openalex-snapshot

Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with the antipsychotic drug sulpiride

inferredcites →https://doi.org/10.1016/j.bmcl.2003.12.029openalex-snapshot

Carbonic anhydrase inhibitors: The first selective, membrane-impermeant inhibitors targeting the tumor-associated isozyme IX

inferredcites →https://doi.org/10.1016/j.bmcl.2004.01.095openalex-snapshot

Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozyme IX with fluorine-containing sulfonamides. The first subnanomolar CA IX inhibitor discovered

inferredcites →https://doi.org/10.1016/j.bmcl.2004.06.073openalex-snapshot

Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the methanoarchaeon Methanobacterium thermoautotrophicum (Cab) with anions

inferredcites →https://doi.org/10.1016/j.bmcl.2004.07.087openalex-snapshot

Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating 1,2,4-triazine moieties

inferredcites →https://doi.org/10.1016/j.bmcl.2004.09.062openalex-snapshot

Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides derived from 4-isothiocyanato-benzolamide

inferredcites →https://doi.org/10.1016/j.bmcl.2004.09.085openalex-snapshot

Carbonic anhydrase inhibitors. Inhibition of the prokariotic beta and gamma-class enzymes from Archaea with sulfonamides

inferredcites →https://doi.org/10.1016/j.bmcl.2004.11.058openalex-snapshot

Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with bis-sulfamates

inferredcites →https://doi.org/10.1016/j.bmcl.2004.12.009openalex-snapshot

Carbonic anhydrase inhibitors. Inhibition of the membrane-bound human and bovine isozymes IV with sulfonamides

inferredcites →https://doi.org/10.1016/j.bmcl.2004.12.052openalex-snapshot

Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides

inferredcites →https://doi.org/10.1016/j.bmcl.2004.12.053openalex-snapshot

Carbonic anhydrase inhibitors. Inhibition of the transmembrane isozyme XII with sulfonamides—a new target for the design of antitumor and antiglaucoma drugs?

inferredcites →https://doi.org/10.1016/j.bmcl.2005.02.091openalex-snapshot

Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, IX, and XII with N-hydroxysulfamides—a new zinc-binding function in the design of inhibitors

inferredcites →https://doi.org/10.1016/j.bmcl.2005.03.032openalex-snapshot

Carbonic anhydrase inhibitors. Zonisamide is an effective inhibitor of the cytosolic isozyme II and mitochondrial isozyme V: solution and X-ray crystallographic studies

inferredcites →https://doi.org/10.1016/j.bmcl.2005.04.058openalex-snapshot

Carbonic anhydrase inhibitors. Synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with boron-containing sulfonamides, sulfamides, and sulfamates: Toward agents for boron neutron capture therapy of hypoxic tumors

inferredcites →https://doi.org/10.1016/j.bmcl.2005.06.055openalex-snapshot

Carbonic anhydrase inhibitors: Inhibition of the transmembrane isozyme XIV with sulfonamides

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Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II ‘selective’ inhibitor celecoxib

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Carbonic anhydrase activators: Activation of isozyme XIII with amino acids and amines

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Carbonic anhydrase inhibitors. Inhibition of the cytosolic human isozymes I and II, and the transmembrane, tumor-associated isozymes IX and XII with substituted aromatic sulfonamides activatable in hypoxic tumors

inferredcites →https://doi.org/10.1016/j.bmcl.2006.07.021openalex-snapshot

Carbonic anhydrase activators: The first X-ray crystallographic study of an adduct of isoform I

inferredcites →https://doi.org/10.1016/j.bmcl.2006.11.027openalex-snapshot

Carbonic anhydrase activators: l-Adrenaline plugs the active site entrance of isozyme II, activating better isoforms I, IV, VA, VII, and XIV

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inferredcites →https://doi.org/10.1016/j.bone.2006.11.028openalex-snapshot

Membrane-bound carbonic anhydrases in osteoclasts

inferredcites →https://doi.org/10.1016/j.canlet.2007.01.012openalex-snapshot

Genome-wide expression analysis using microarray identified complex signaling pathways modulated by hypoxia in nasopharyngeal carcinoma

inferredcites →https://doi.org/10.1016/j.cub.2005.09.047openalex-snapshot

Carbonic Anhydrase and CO2 Sensing during Cryptococcus neoformans Growth, Differentiation, and Virulence

inferredcites →https://doi.org/10.1016/j.cub.2005.10.040openalex-snapshot

Fungal Adenylyl Cyclase Integrates CO2 Sensing with cAMP Signaling and Virulence

inferredcites →https://doi.org/10.1016/j.febslet.2004.10.043openalex-snapshot

Hypoxia activates the capacity of tumor‐associated carbonic anhydrase IX to acidify extracellular pH

inferredcites →https://doi.org/10.1016/j.febslet.2007.06.018openalex-snapshot

Oxygen, a source of life and stress

inferredcites →https://doi.org/10.1016/j.ijrobp.2003.10.016openalex-snapshot

Hypoxia-activated tumor pathways of angiogenesis and pH regulation independent of anemia in head-and-neck cancer

inferredcites →https://doi.org/10.1016/j.juro.2007.03.112openalex-snapshot

An Investigation Into the Prognostic Significance of Necrosis and Hypoxia in High Grade and Invasive Bladder Cancer

inferredcites →https://doi.org/10.1016/j.radonc.2007.04.018openalex-snapshot

Imaging the hypoxia surrogate marker CA IX requires expression and catalytic activity for binding fluorescent sulfonamide inhibitors

inferredcites →https://doi.org/10.1016/j.tips.2006.09.002openalex-snapshot

Targeting tumor-associated carbonic anhydrase IX in cancer therapy

inferredcites →https://doi.org/10.1016/s0022-3565(24)29621-xopenalex-snapshot

Pharmacological Enhancement of Synaptic Efficacy, Spatial Learning, and Memory through Carbonic Anhydrase Activation in Rats

inferredcites →https://doi.org/10.1016/s0165-6147(02)01899-0openalex-snapshot

Carbonic anhydrase gating of attention: memory therapy and enhancement

inferredcites →https://doi.org/10.1016/s0168-6445(00)00030-9openalex-snapshot

Prokaryotic carbonic anhydrases

inferredcites →https://doi.org/10.1016/s0223-5234(98)80042-1openalex-snapshot

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

inferredcites →https://doi.org/10.1016/s0960-894x(02)00121-xopenalex-snapshot

Carbonic anhydrase activators: Human isozyme II is strongly activated by oligopeptides incorporating the carboxyterminal sequence of the bicarbonate anion exchanger AE1

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Carbonic anhydrase inhibitors: SAR and X-ray crystallographic study for the interaction of sugar sulfamates/sulfamides with isozymes I, II and IV

inferredcites →https://doi.org/10.1016/s0960-894x(03)00091-xopenalex-snapshot

Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozyme IX with aromatic and heterocyclic sulfonamides

inferredcites →https://doi.org/10.1016/s0968-0896(00)00143-7openalex-snapshot

Carbonic anhydrase inhibitors: sulfonamides incorporating furan-, thiophene- and pyrrole-carboxamido groups possess strong topical intraocular pressure lowering properties as aqueous suspensions

inferredcites →https://doi.org/10.1016/s0968-0896(99)00227-8openalex-snapshot

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

inferredcites →https://doi.org/10.1016/s1350-9462(99)00006-3openalex-snapshot

Pharmacological and ocular hypotensive properties of topical carbonic anhydrase inhibitors

inferredcites →https://doi.org/10.1021/bi970760vopenalex-snapshot

Carbonic Anhydrase Activators: X-ray Crystallographic and Spectroscopic Investigations for the Interaction of Isozymes I and II with Histamine,

inferredcites →https://doi.org/10.1021/ja061574sopenalex-snapshot

Carbonic Anhydrase Inhibitors: X-ray and Molecular Modeling Study for the Interaction of a Fluorescent Antitumor Sulfonamide with Isozyme II and IX

inferredcites →https://doi.org/10.1021/jm000296jopenalex-snapshot

Carbonic Anhydrase Inhibitors: Perfluoroalkyl/Aryl-Substituted Derivatives of Aromatic/Heterocyclic Sulfonamides as Topical Intraocular Pressure-Lowering Agents with Prolonged Duration of Action

inferredcites →https://doi.org/10.1021/jm0108202openalex-snapshot

Carbonic Anhydrase Inhibitors. A General Approach for the Preparation of Water-Soluble Sulfonamides Incorporating Polyamino−Polycarboxylate Tails and of Their Metal Complexes Possessing Long-Lasting, Topical Intraocular Pressure-Lowering Properties

inferredcites →https://doi.org/10.1021/jm010958kopenalex-snapshot

Carbonic Anhydrase Activators: High Affinity Isozymes I, II, and IV Activators, Incorporating a β-Alanyl-histidine Scaffold

inferredcites →https://doi.org/10.1021/jm011031nopenalex-snapshot

Carbonic Anhydrase Activators: Design of High Affinity Isozymes I, II, and IV Activators, Incorporating Tri-/Tetrasubstituted-pyridinium-azole Moieties

inferredcites →https://doi.org/10.1021/jm0201060openalex-snapshot

Array-Based Structure and Gene Expression Relationship Study of Antitumor Sulfonamides IncludingN-[2-[(4-Hydroxyphenyl)amino]-3-pyridinyl]-4-methoxybenzenesulfonamide andN-(3-Chloro-7-indolyl)-1,4-benzenedisulfonamide

inferredcites →https://doi.org/10.1021/jm021123sopenalex-snapshot

Carbonic Anhydrase Inhibitors. Inhibition of Tumor-Associated Isozyme IX by Halogenosulfanilamide and Halogenophenylaminobenzolamide Derivatives

inferredcites →https://doi.org/10.1021/jm021124kopenalex-snapshot

Carbonic Anhydrase Inhibitors. Inhibition of Cytosolic Isozymes I and II and Transmembrane, Tumor-Associated Isozyme IX with Sulfamates Including EMATE Also Acting as Steroid Sulfatase Inhibitors

inferredcites →https://doi.org/10.1021/jm030911uopenalex-snapshot

Carbonic Anhydrase Inhibitors: Inhibition of Transmembrane, Tumor-Associated Isozyme IX, and Cytosolic Isozymes I and II with Aliphatic Sulfamates

inferredcites →https://doi.org/10.1021/jm031057+openalex-snapshot

Carbonic Anhydrase Inhibitors. Inhibition of Mitochondrial Isozyme V with Aromatic and Heterocyclic Sulfonamides

inferredcites →https://doi.org/10.1021/jm031079wopenalex-snapshot

Carbonic Anhydrase Inhibitors. Design of Selective, Membrane-Impermeant Inhibitors Targeting the Human Tumor-Associated Isozyme IX

inferredcites →https://doi.org/10.1021/jm0494826openalex-snapshot

Carbonic Anhydrase Inhibitors: Synthesis and Inhibition of Cytosolic/Membrane-Associated Carbonic Anhydrase Isozymes I, II, and IX with Sulfonamides Incorporating Hydrazino Moieties

inferredcites →https://doi.org/10.1021/jm049692iopenalex-snapshot

Carbonic Anhydrase Inhibitors: The First On-Resin Screening of a 4-Sulfamoylphenylthiourea Library

inferredcites →https://doi.org/10.1021/jm0501073openalex-snapshot

Carbonic Anhydrase Inhibitors. Design of Fluorescent Sulfonamides as Probes of Tumor-Associated Carbonic Anhydrase IX That Inhibit Isozyme IX-Mediated Acidification of Hypoxic Tumors

inferredcites →https://doi.org/10.1021/jm050333copenalex-snapshot

Carbonic Anhydrase Inhibitors: Stacking with Phe131 Determines Active Site Binding Region of Inhibitors As Exemplified by the X-ray Crystal Structure of a Membrane-Impermeant Antitumor Sulfonamide Complexed with Isozyme II

inferredcites →https://doi.org/10.1021/jm050483nopenalex-snapshot

Carbonic Anhydrase Inhibitors. The Mitochondrial Isozyme VB as a New Target for Sulfonamide and Sulfamate Inhibitors

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Carbonic Anhydrase Inhibitors: DNA Cloning and Inhibition Studies of the α-Carbonic Anhydrase from Helicobacter pylori, A New Target for Developing Sulfonamide and Sulfamate Gastric Drugs

inferredcites →https://doi.org/10.1021/jm0600287openalex-snapshot

Indanesulfonamides as Carbonic Anhydrase Inhibitors. Toward Structure-Based Design of Selective Inhibitors of the Tumor-Associated Isozyme CA IX

inferredcites →https://doi.org/10.1021/jm0603320openalex-snapshot

Carbonic Anhydrase Activators. Activation of Isoforms I, II, IV, VA, VII, and XIV with l - and d -Phenylalanine and Crystallographic Analysis of Their Adducts with Isozyme II: Stereospecific Recognition within the Active Site of an Enzyme and Its Consequences for the Drug Design

inferredcites →https://doi.org/10.1021/jm060531jopenalex-snapshot

Carbonic Anhydrase Inhibitors: Hypoxia-Activatable Sulfonamides Incorporating Disulfide Bonds that Target the Tumor-Associated Isoform IX

inferredcites →https://doi.org/10.1021/jm060807nopenalex-snapshot

Carbonic Anhydrase Inhibitors: Clash with Ala65 as a Means for Designing Inhibitors with Low Affinity for the Ubiquitous Isozyme II, Exemplified by the Crystal Structure of the Topiramate Sulfamide Analogue

inferredcites →https://doi.org/10.1021/jm060967zopenalex-snapshot

A Novel Class of Carbonic Anhydrase Inhibitors: Glycoconjugate Benzene Sulfonamides Prepared by “Click-Tailing”

inferredcites →https://doi.org/10.1021/jm0612057openalex-snapshot

Carbonic Anhydrase Inhibitors. DNA Cloning, Characterization, and Inhibition Studies of the Human Secretory Isoform VI, a New Target for Sulfonamide and Sulfamate Inhibitors

inferredcites →https://doi.org/10.1021/jm061320hopenalex-snapshot

Carbonic Anhydrase Inhibitors: Inhibition of Isozymes I, II, and IX with Triazole-Linked O-Glycosides of Benzene Sulfonamides

inferredcites →https://doi.org/10.1021/jm9900523openalex-snapshot

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?

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

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Discovery of Novel Antitumor Sulfonamides Targeting G1 Phase of the Cell Cycle

inferredcites →https://doi.org/10.1021/jm990479+openalex-snapshot

Carbonic Anhydrase Inhibitors: Synthesis of Membrane-Impermeant Low Molecular Weight Sulfonamides Possessing in Vivo Selectivity for the Membrane-Bound versus Cytosolic Isozymes

inferredcites →https://doi.org/10.1038/20459openalex-snapshot

The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis

inferredcites →https://doi.org/10.1038/82113openalex-snapshot

Targeting tumors through the HIF system

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Structural basis for the recognition of hydroxyproline in HIF-1α by pVHL

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Hypoxia signalling in cancer and approaches to enforce tumour regression

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Extracellular carbonic anhydrase mediates hemorrhagic retinal and cerebral vascular permeability through prekallikrein activation

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Topiramate Reduces Energy and Fat Gains in Lean (Fa/?) and Obese (fa/fa) Zucker Rats

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Diagnostic, prognostic and therapeutic implications of carbonic anhydrases in cancer

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Hypoxia-regulated carbonic anhydrase IX expression is associated with poor survival in patients with invasive breast cancer

inferredcites →https://doi.org/10.1042/bj20050556openalex-snapshot

Carbonic anhydrase (Nce103p): an essential biosynthetic enzyme for growth of Saccharomyces cerevisiae at atmospheric carbon dioxide pressure

inferredcites →https://doi.org/10.1074/jbc.m308984200openalex-snapshot

Characterization of CA XIII, a Novel Member of the Carbonic Anhydrase Isozyme Family

inferredcites →https://doi.org/10.1074/jbc.m414348200openalex-snapshot

Structure and Function of Carbonic Anhydrases from Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1080/07357900601062321openalex-snapshot

Role of Carbonic Anhydrases in the Progression of Renal Cell Carcinoma Subtypes: Proposal of a Unified Hypothesis

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Carbonic Anhydrase Inhibitors: Synthesis of Sulfonamides Incorporating 2, 4, 6–Trisubstituted-Pyridinium-Ethylcarboxamido Moieties Possessing Membrane-Impermeability and in Vivo Selectivity for the Membrane-Bound (CA IV) Versus the Cytosolic (CA I and CA II) Isozymes

inferredcites →https://doi.org/10.1080/14756360410001689540openalex-snapshot

Review Article

inferredcites →https://doi.org/10.1097/00061198-199502000-00012openalex-snapshot

The Development of Topical Carbonic Anhydrase Inhibitors

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Targeting of HIF-α to the von Hippel-Lindau Ubiquitylation Complex by O 2 -Regulated Prolyl Hydroxylation

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Identification and Preliminary Characterization of Two cDNAs Encoding Unique Carbonic Anhydrases from the Marine Alga Emiliania huxleyi

inferredcites →https://doi.org/10.1128/ec.5.1.103-111.2006openalex-snapshot

Cryptococcus neoformans Senses CO 2 through the Carbonic Anhydrase Can2 and the Adenylyl Cyclase Cac1

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Expression of cell surface transmembrane carbonic anhydrase genes CA9 and CA12 in the human eye: overexpression of CA12 (CAXII) in glaucoma

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Hypoxia-Inducible Factor 1α Expression as an Intrinsic Marker of Hypoxia

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A Randomized Phase II Pharmacokinetic and Pharmacodynamic Study of Indisulam as Second-Line Therapy in Patients with Advanced Non–Small Cell Lung Cancer

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Localization of Carbonic Anhydrase XII to the Basolateral Membrane of H + -secreting Cells of Mouse and Rat Kidney

inferredcites →https://doi.org/10.1200/jco.2003.11.132openalex-snapshot

Carbonic Anhydrase IX Expression, a Novel Surrogate Marker of Tumor Hypoxia, Is Associated With a Poor Prognosis in Non–Small-Cell Lung Cancer

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Acatalytic CAs

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Cancer-Related Carbonic Anhydrase Isozymes and Their Inhibition

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Carbonic anhydrase inhibitors in the treatment and prophylaxis of obesity

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Carbonic anhydrase inhibitors and activators and their use in therapy

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COX-2 Selective Inhibitors, Carbonic Anhydrase Inhibition and Anticancer Properties of Sulfonamides Belonging to This Class of Pharmacological Agents

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Antiviral Sulfonamide Derivatives

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The Development of Topically Acting Carbonic Anhydrase Inhibitors as Antiglaucoma Agents

inferredcites →https://doi.org/10.2174/156802607780636753openalex-snapshot

Inhibition of the Archaeal β-Class (Cab) and γ-Class (Cam) Carbonic Anhydrases

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Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II "selective" inhibitor Celecoxib

inferredcites →https://doi.org/10.4155/fmc-2017-0223openalex-snapshot

Carbonic Anhydrase Activators

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Carbonic Anhydrase

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Synthesis and Characterization of Nicotinamide Complexes of Furan-2-Carboxylates with Some Metals, in Vitro and in Silico Studies on Ca I, Ca Ii, Ache, Bche, Gr Enzymes

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Matching chemical properties to molecular biological activities opens a new perspective on l ‐ergothioneine

inferred← citeshttps://doi.org/10.1002/2211-5463.13847openalex-snapshot

Structural information in therapeutic peptides: Emerging applications in biomedicine

inferred← citeshttps://doi.org/10.1002/9780470508169openalex-snapshot

Drug Design of Zinc‐Enzyme Inhibitors

inferred← citeshttps://doi.org/10.1002/9780470508169.ch1openalex-snapshot

Introduction to Zinc Enzymes as Drug Targets

inferred← citeshttps://doi.org/10.1002/9780470508169.ch10openalex-snapshot

Drug Design of Antiobesity Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/9780470508169.ch12openalex-snapshot

Advances in the Inhibitory and Structural Investigations on Carbonic Anhydrase Isozymes XIII and XV

inferred← citeshttps://doi.org/10.1002/9780470508169.ch14openalex-snapshot

Fungal and Nematode Carbonic Anhydrases: Their Inhibition in Drug Design

inferred← citeshttps://doi.org/10.1002/9780470508169.ch15openalex-snapshot

Crystallographic Studies on Carbonic Anhydrases from Fungal Pathogens for Structure‐Assisted Drug Development

inferred← citeshttps://doi.org/10.1002/9780470508169.ch16openalex-snapshot

Malaria Parasite Carbonic Anhydrase and Its Inhibition in the Development of Novel Therapies of Malaria

inferred← citeshttps://doi.org/10.1002/9780470508169.ch18openalex-snapshot

QSAR of Carbonic Anhydrase Inhibitors and Their Impact on Drug Design

inferred← citeshttps://doi.org/10.1002/9780470508169.ch19openalex-snapshot

Selectivity Issues in the Design of CA Inhibitors

inferred← citeshttps://doi.org/10.1002/9780470508169.ch2openalex-snapshot

Carbonic Anhydrases as Drug Targets: General Presentation

inferred← citeshttps://doi.org/10.1002/9780470508169.ch21openalex-snapshot

Metal Complexes of Sulfonamides as Dual Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/9780470508169.ch29openalex-snapshot

Botulinus Toxin, Tetanus Toxin, and Anthrax Lethal Factor Inhibitors

inferred← citeshttps://doi.org/10.1002/9780470508169.ch3openalex-snapshot

Zinc Binding Functions in the Design of Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/9780470508169.ch4openalex-snapshot

X‐Ray Crystallography of Carbonic Anhydrase Inhibitors and Its Importance in Drug Design

inferred← citeshttps://doi.org/10.1002/9780470508169.ch5openalex-snapshot

Antiglaucoma Carbonic Anhydrase Inhibitors as Ophthalomologic Drugs

inferred← citeshttps://doi.org/10.1002/9780470508169.ch6openalex-snapshot

Diuretics with Carbonic Anhydrase Inhibitory Activity: Toward Novel Applications for Sulfonamide Drugs

inferred← citeshttps://doi.org/10.1002/9780470508169.ch8openalex-snapshot

Carbonic Anhydrase Inhibitors Targeting Cancer: Therapeutic, Immunologic, and Diagnostic Tools Targeting Isoforms IX and XII

inferred← citeshttps://doi.org/10.1002/9780470508169.ch9openalex-snapshot

Fluorescent‐ and Spin‐Labeled Sulfonamides as Probe for Carbonic Anhydrase IX

inferred← citeshttps://doi.org/10.1002/9780470551554.ch7openalex-snapshot

Dynamic Combinatorial Chemistry and Mass Spectrometry: A Combined Strategy for High Performance Lead Discovery

inferred← citeshttps://doi.org/10.1002/9781118098141.ch23openalex-snapshot

Carbonic Anhydrases: Off Targets, Add‐On Activities, or Emerging Novel Targets?

inferred← citeshttps://doi.org/10.1002/9781118854754.ch6openalex-snapshot

The Radiopharmaceutical Chemistry of Technetium and Rhenium

inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0688openalex-snapshot

Cadmium‐Carbonic Anhydrase

inferred← citeshttps://doi.org/10.1002/9783527633104.ch12openalex-snapshot

Metal Compounds as Enzyme Inhibitors

inferred← citeshttps://doi.org/10.1002/9783527664450.ch11openalex-snapshot

Thiazide‐Based Diuretics for the Treatment of Hypertension and Genitourinary Disorders

inferred← citeshttps://doi.org/10.1002/9783527665211.ch19openalex-snapshot

Carbonic Anhydrase Inhibitors for the Treatment of Glaucoma: Design and Discovery of Dorzolamide

inferred← citeshttps://doi.org/10.1002/9783527673438.ch01openalex-snapshot

Organometallic Complexes as Enzyme Inhibitors: A Conceptual Overview

inferred← citeshttps://doi.org/10.1002/9783527676132.ch3openalex-snapshot

Developing Novel Bacterial Targets: Carbonic Anhydrases as Antibacterial Drug Targets

inferred← citeshttps://doi.org/10.1002/adfm.201402118openalex-snapshot

Plasmonic Particles that Hit Hypoxic Cells

inferred← citeshttps://doi.org/10.1002/adfm.201908365openalex-snapshot

Amorphous Fe‐Based Nanoagents for Self‐Enhanced Chemodynamic Therapy by Re‐Establishing Tumor Acidosis

inferred← citeshttps://doi.org/10.1002/adsc.201900573openalex-snapshot

Iridium‐Catalyzed ortho‐C−H Amidation of Benzenesulfonamides with Sulfonyl Azides

inferred← citeshttps://doi.org/10.1002/advs.202001970openalex-snapshot

A Single‐Stranded DNA‐Encoded Chemical Library Based on a Stereoisomeric Scaffold Enables Ligand Discovery by Modular Assembly of Building Blocks

inferred← citeshttps://doi.org/10.1002/advs.202207490openalex-snapshot

Nanomedicines Reprogram Synovial Macrophages by Scavenging Nitric Oxide and Silencing CA9 in Progressive Osteoarthritis

inferred← citeshttps://doi.org/10.1002/alz.70023openalex-snapshot

Carbonic anhydrase inhibitors prevent presymptomatic capillary flow disturbances in a model of cerebral amyloidosis

inferred← citeshttps://doi.org/10.1002/ange.201107333openalex-snapshot

[(Cp‐R)M(CO)3] (M=Re or 99mTc) Arylsulfonamide, Arylsulfamide, and Arylsulfamate Conjugates for Selective Targeting of Human Carbonic Anhydrase IX

inferred← citeshttps://doi.org/10.1002/ange.201307583openalex-snapshot

Carborane‐Based Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/ange.201410736openalex-snapshot

Identification of Structure–Activity Relationships from Screening a Structurally Compact DNA‐Encoded Chemical Library

inferred← citeshttps://doi.org/10.1002/ange.201508990openalex-snapshot

Programming A Molecular Relay for Ultrasensitive Biodetection through 129Xe NMR

inferred← citeshttps://doi.org/10.1002/ange.201903968openalex-snapshot

Organic Photodynamic Nanoinhibitor for Synergistic Cancer Therapy

inferred← citeshttps://doi.org/10.1002/ange.201913436openalex-snapshot

Drug Screening in Human Cells by NMR Spectroscopy Allows the Early Assessment of Drug Potency

inferred← citeshttps://doi.org/10.1002/ange.201914826openalex-snapshot

A Fluorescent Probe for Rapid, High‐Contrast Visualization of Folate‐Receptor‐Expressing Tumors In Vivo

inferred← citeshttps://doi.org/10.1002/ange.202005362openalex-snapshot

CAIXplatins: Highly Potent Platinum(IV) Prodrugs Selective Against Carbonic Anhydrase IX for the Treatment of Hypoxic Tumors

inferred← citeshttps://doi.org/10.1002/ange.202103211openalex-snapshot

Modulating the Efficacy of Carbonic Anhydrase Inhibitors through Fluorine Substitution

inferred← citeshttps://doi.org/10.1002/ange.202115800openalex-snapshot

A Carbonic Anhydrase IX (CAIX)‐Anchored Rhenium(I) Photosensitizer Evokes Pyroptosis for Enhanced Anti‐Tumor Immunity

inferred← citeshttps://doi.org/10.1002/ange.202206797openalex-snapshot

Diversification of Aryl Sulfonyl Compounds through Ligand‐Controlledmeta‐ andpara‐C−H Borylation

inferred← citeshttps://doi.org/10.1002/ange.202511839openalex-snapshot

Rational Design Strategies in DNA‐Encoded Libraries for Drug Discovery

inferred← citeshttps://doi.org/10.1002/ange.3685338openalex-snapshot

Ein Ruthenium(CAAC‐5)‐Olefin‐Metathese‐Katalysator für die Biokonjugation

inferred← citeshttps://doi.org/10.1002/anie.201107333openalex-snapshot

[(Cp‐R)M(CO)3] (M=Re or 99mTc) Arylsulfonamide, Arylsulfamide, and Arylsulfamate Conjugates for Selective Targeting of Human Carbonic Anhydrase IX

inferred← citeshttps://doi.org/10.1002/anie.201307583openalex-snapshot

Carborane‐Based Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/anie.201410736openalex-snapshot

Identification of Structure–Activity Relationships from Screening a Structurally Compact DNA‐Encoded Chemical Library

inferred← citeshttps://doi.org/10.1002/anie.201508990openalex-snapshot

Programming A Molecular Relay for Ultrasensitive Biodetection through 129Xe NMR

inferred← citeshttps://doi.org/10.1002/anie.201903968openalex-snapshot

Organic Photodynamic Nanoinhibitor for Synergistic Cancer Therapy

inferred← citeshttps://doi.org/10.1002/anie.201913436openalex-snapshot

Drug Screening in Human Cells by NMR Spectroscopy Allows the Early Assessment of Drug Potency

inferred← citeshttps://doi.org/10.1002/anie.201914826openalex-snapshot

A Fluorescent Probe for Rapid, High‐Contrast Visualization of Folate‐Receptor‐Expressing Tumors In Vivo

inferred← citeshttps://doi.org/10.1002/anie.202005362openalex-snapshot

CAIXplatins: Highly Potent Platinum(IV) Prodrugs Selective Against Carbonic Anhydrase IX for the Treatment of Hypoxic Tumors

inferred← citeshttps://doi.org/10.1002/anie.202103211openalex-snapshot

Modulating the Efficacy of Carbonic Anhydrase Inhibitors through Fluorine Substitution

inferred← citeshttps://doi.org/10.1002/anie.202115800openalex-snapshot

A Carbonic Anhydrase IX (CAIX)‐Anchored Rhenium(I) Photosensitizer Evokes Pyroptosis for Enhanced Anti‐Tumor Immunity

inferred← citeshttps://doi.org/10.1002/anie.202206797openalex-snapshot

Diversification of Aryl Sulfonyl Compounds through Ligand‐Controlledmeta‐ andpara‐C−H Borylation

inferred← citeshttps://doi.org/10.1002/anie.202511839openalex-snapshot

Rational Design Strategies in DNA‐Encoded Libraries for Drug Discovery

inferred← citeshttps://doi.org/10.1002/anie.3685338openalex-snapshot

A Ruthenium(CAAC‐5) Olefin Metathesis Catalyst for Bioconjugation

inferred← citeshttps://doi.org/10.1002/ansa.70091openalex-snapshot

A Selective Phenyl Azo Acetate Substrate for Enhanced Carbonic Anhydrase Functional Analysis

inferred← citeshttps://doi.org/10.1002/aoc.1807openalex-snapshot

Sulfonamide‐derived compounds and their transition metal complexes: synthesis, biological evaluation and X‐ray structure of 4‐bromo‐2‐[(E)‐{4‐[(3,4‐dimethylisoxazol‐5 yl)sulfamoyl]phenyl} iminiomethyl] phenolate

inferred← citeshttps://doi.org/10.1002/ardp.201200160openalex-snapshot

Synthesis and Antimicrobial Activity of Novel Heterocyclic Sulfamoyl‐phenyl‐carboximidamides Derived from Clinically Applied Sulfonamides

inferred← citeshttps://doi.org/10.1002/ardp.201300054openalex-snapshot

Synthesis and Biological Evaluation of Novel Bromophenol Derivatives as Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.201300228openalex-snapshot

Synthesis, Antioxidant, and Antiacetylcholinesterase Activities of Sulfonamide Derivatives of Dopamine‐ R elated Compounds

inferred← citeshttps://doi.org/10.1002/ardp.201300273openalex-snapshot

Novel Sulphamides and Sulphonamides Incorporating the Tetralin Scaffold as Carbonic Anhydrase and Acetylcholine Esterase Inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.201300349openalex-snapshot

Synthesis and Carbonic Anhydrase Isoenzymes Inhibitory Effects of Brominated Diphenylmethanone and Its Derivatives

inferred← citeshttps://doi.org/10.1002/ardp.201400257openalex-snapshot

Synthesis and Carbonic Anhydrase Inhibitory Effects of Novel Sulfamides Derived from 1‐Aminoindanes and Anilines

inferred← citeshttps://doi.org/10.1002/ardp.201400330openalex-snapshot

Synthesis and Determination of Some Biological Activities of Novel 2,4‐Dinitrophenyl Derivatives

inferred← citeshttps://doi.org/10.1002/ardp.201600047openalex-snapshot

9,10‐Dibromo‐N‐aryl‐9,10‐dihydro‐9,10‐[3,4]epipyrroloanthracene‐12,14‐diones: Synthesis and Investigation of Their Effects on Carbonic Anhydrase Isozymes I, II, IX, and XII

inferred← citeshttps://doi.org/10.1002/ardp.201600092openalex-snapshot

Synthesis and Carbonic Anhydrase Inhibition of Novel 2‐(4‐(Aryl)thiazole‐2‐yl)‐3a,4,7,7a‐tetrahydro‐1H‐4,7‐methanoisoindole‐1,3(2H)‐dione Derivatives

inferred← citeshttps://doi.org/10.1002/ardp.201600122openalex-snapshot

Synthesis and Biological Evaluation of Novel Bischalcone Derivatives as Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.201700045openalex-snapshot

Novel NHC Precursors: Synthesis, Characterization, and Carbonic Anhydrase and Acetylcholinesterase Inhibitory Properties

inferred← citeshttps://doi.org/10.1002/ardp.201700198openalex-snapshot

Synthesis and Carbonic Anhydrase Inhibition of Tetrabromo Chalcone Derivatives

inferred← citeshttps://doi.org/10.1002/ardp.201800029openalex-snapshot

meta‐Cyanobenzyl substituted benzimidazolium salts: Synthesis, characterization, crystal structure and carbonic anhydrase, α‐glycosidase, butyrylcholinesterase, and acetylcholinesterase inhibitory properties

inferred← citeshttps://doi.org/10.1002/ardp.201900200openalex-snapshot

Synthesis of β‐amino acid derivatives and their inhibitory profiles against some metabolic enzymes

inferred← citeshttps://doi.org/10.1002/ardp.202000102openalex-snapshot

Synthesis, characterization, biological evaluation, and in silico studies of novel 1,3‐diaryltriazene‐substituted sulfathiazole derivatives

inferred← citeshttps://doi.org/10.1002/ardp.202000230openalex-snapshot

Synthesis of benzamide derivatives with thiourea‐substituted benzenesulfonamides as carbonic anhydrase inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202000291openalex-snapshot

Potential antibacterial and antifungal activities of novel sulfamidophosphonate derivatives bearing the quinoline or quinolone moiety

inferred← citeshttps://doi.org/10.1002/ardp.202000375openalex-snapshot

Synthesis and in vitro carbonic anhydrases and acetylcholinesterase inhibitory activities of novel imidazolinone‐based benzenesulfonamides

inferred← citeshttps://doi.org/10.1002/ardp.202100113openalex-snapshot

Synthesis and biological evaluation of some 1‐naphthol derivatives as antioxidants, acetylcholinesterase, and carbonic anhydrase inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202100122openalex-snapshot

Synthesis of new 7‐amino‐3,4‐dihydroquinolin‐2(1H)‐one‐peptide derivatives and their carbonic anhydrase enzyme inhibition, antioxidant, and cytotoxic activities

inferred← citeshttps://doi.org/10.1002/ardp.202100241openalex-snapshot

Novel benzenesulfonamide‐bearing pyrazoles and 1,2,4‐thiadiazoles as selective carbonic anhydrase inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202100333openalex-snapshot

Design and development of novel series of indole‐3‐sulfonamide ureido derivatives as selective carbonic anhydrase II inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202100476openalex-snapshot

Some phenolic natural compounds as carbonic anhydrase inhibitors: An in vitro and in silico study

inferred← citeshttps://doi.org/10.1002/ardp.202200019openalex-snapshot

Design, synthesis, SAR, and biological evaluation of saccharin‐based hybrids as carbonic anhydrase inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202200023openalex-snapshot

New 1H‐indole‐2,3‐dione 3‐thiosemicarbazones with 3‐sulfamoylphenyl moiety as selective carbonic anhydrase inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202200391openalex-snapshot

Benzenesulfonamides with trisubstituted triazole motif as selective carbonic anhydrase I, II, IV, and IX inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202200434openalex-snapshot

Novel benzenesulfonamide‐thiouracil conjugates with a flexible N‐ethyl acetamide linker as selective CA IX and CA XII inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202200508openalex-snapshot

Coumaryl‐sulfonamide moiety: Unraveling their synthetic strategy and specificity toward h CA IX/XII, facilitating anticancer drug development

inferred← citeshttps://doi.org/10.1002/ardp.202300205openalex-snapshot

Design, synthesis, and structure–activity studies of new rhodanine derivatives as carbonic anhydrase II, IX inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202300266openalex-snapshot

Efficient, rapid, and high‐yield synthesis of aryl Schiff base derivatives and their in vitro and in silico inhibition studies of hCA I, hCA II, AChE, and BuChE

inferred← citeshttps://doi.org/10.1002/ardp.202300349openalex-snapshot

Potent inhibitors of tumor associated carbonic anhydrases endowed with cathepsin B inhibition

inferred← citeshttps://doi.org/10.1002/ardp.202300372openalex-snapshot

1,2,3‐Triazole‐based esters and carboxylic acids as nonclassical carbonic anhydrase inhibitors capable of cathepsin B inhibition

inferred← citeshttps://doi.org/10.1002/ardp.202300374openalex-snapshot

Synthesis and biological evaluation of novel salicylidene uracils: Cytotoxic activity on human cancer cell lines and inhibitory action on enzymatic activity

inferred← citeshttps://doi.org/10.1002/ardp.202300718openalex-snapshot

Design, synthesis, and biological evaluation of 3‐benzenesulfonamide‐linked 3‐hydrazinoisatin derivatives as carbonic anhydrase inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202400038openalex-snapshot

Sulfonamide‐incorporated bis(α‐aminophosphonates) as promising carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and X‐ray crystallographic studies

inferred← citeshttps://doi.org/10.1002/ardp.202400064openalex-snapshot

Exploring rhodanine linked enamine–carbohydrazide derivatives as mycobacterial carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and molecular docking studies

inferred← citeshttps://doi.org/10.1002/ardp.202400069openalex-snapshot

Chalcone‐based benzenesulfonamides as potent and selective inhibitors for human carbonic anhydrase II: Design, synthesis, in vitro, and in silico studies

inferred← citeshttps://doi.org/10.1002/ardp.202400114openalex-snapshot

Benzenesulfonamides functionalized with triazolyl‐linked pyrazoles possess dual cathepsin B and carbonic anhydrase inhibitory action

inferred← citeshttps://doi.org/10.1002/ardp.202400157openalex-snapshot

In‐vitro and in‐silico investigations of SLC‐0111 hydrazinyl analogs as human carbonic anhydrase I, II, IX, and XII inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202400259openalex-snapshot

Benzothiazole derivatives in the design of antitumor agents

inferred← citeshttps://doi.org/10.1002/ardp.202400366openalex-snapshot

Novel thiazolotriazole and triazolothiadiazine scaffolds as selective tumor associated carbonic anhydrase inhibitors endowed with cathepsin B inhibition

inferred← citeshttps://doi.org/10.1002/ardp.202400482openalex-snapshot

New 7‐hydroxycoumarin acetamide derivatives as human carbonic anhydrase IX and XII inhibitors: Design, synthesis, biological evaluation and molecular docking studies

inferred← citeshttps://doi.org/10.1002/ardp.202400626openalex-snapshot

The carbonic anhydrase enzymes as new targets for the management of neglected tropical diseases

inferred← citeshttps://doi.org/10.1002/ardp.202400705openalex-snapshot

Lactonase activity of α‐carbonic anhydrases allows identification of novel inhibitors

inferred← citeshttps://doi.org/10.1002/ardp.202400748openalex-snapshot

Unveiling tomorrow: Carbonic anhydrase activators and inhibitors pioneering new frontiers in Alzheimer's disease

inferred← citeshttps://doi.org/10.1002/ardp.202400776openalex-snapshot

Unprecedented carbonic anhydrase inhibition mechanism: Targeting histidine 64 side chain through a halogen bond

inferred← citeshttps://doi.org/10.1002/ardp.202400909openalex-snapshot

Anticholinesterase and carbonic anhydrase inhibitory activities of natural carnosic acid derivatives: A comprehensive in vitro and in silico study

inferred← citeshttps://doi.org/10.1002/ardp.202400963openalex-snapshot

Exploration of Aromatic Hydrazides as Inhibitors of Human Carbonic Anhydrases

inferred← citeshttps://doi.org/10.1002/ardp.70145openalex-snapshot

New Se‐Compounds With Antileishmanial, Antitumor, and Carbonic Anhydrase Inhibitory Properties

inferred← citeshttps://doi.org/10.1002/ardp.70180openalex-snapshot

Exploring Sulfonamides: Biological Activities and Structure–Activity Relationships

inferred← citeshttps://doi.org/10.1002/ardp.70333openalex-snapshot

From Identification to Enzymatic Activity Profiling: Comprehensive Characterization of BloCAβ, a Probiotic β‐Carbonic Anhydrase From Bifidobacterium longum

inferred← citeshttps://doi.org/10.1002/asia.202100060openalex-snapshot

Improved Stabilities of Labeling Probes for the Selective Modification of Endogenous Proteins in Living Cells and In Vivo

inferred← citeshttps://doi.org/10.1002/asia.202400067openalex-snapshot

The dopamine D2 receptors antagonist Veralipride inhibits carbonic anhydrases: solution and crystallographic insights on human isoforms

inferred← citeshttps://doi.org/10.1002/asia.70552openalex-snapshot

Early Transition Metal‐Based Antitumor Complexes

inferred← citeshttps://doi.org/10.1002/bab.2445openalex-snapshot

Synthesis, enzyme inhibition, and molecular docking studies of a novel chalcone series bearing benzothiazole scaffold

inferred← citeshttps://doi.org/10.1002/bab.2534openalex-snapshot

Sulfonamide derivatives with benzothiazole scaffold: Synthesis and carbonic anhydrase I–II inhibition properties

inferred← citeshttps://doi.org/10.1002/bdd.2309openalex-snapshot

In vitro and in silico interactions of antiulcer, glucocorticoids and urological drugs on human carbonic anhydrase I and II isozymes

inferred← citeshttps://doi.org/10.1002/bip.22456openalex-snapshot

The structural comparison between membrane‐associated human carbonic anhydrases provides insights into drug design of selective inhibitors

inferred← citeshttps://doi.org/10.1002/bit.24863openalex-snapshot

Periplasmic expression of carbonic anhydrase in Escherichia coli: A new biocatalyst for CO2 hydration

inferred← citeshttps://doi.org/10.1002/cam4.991openalex-snapshot

Hypoxia‐inducible factor 1 promotes chemoresistance of lung cancer by inducing carbonic anhydrase IX expression

inferred← citeshttps://doi.org/10.1002/cbdv.201700024openalex-snapshot

Carbonic Anhydrase and Urease Inhibitory Potential of Various Plant Phenolics Using in vitro and in silico Methods

inferred← citeshttps://doi.org/10.1002/cbdv.202201146openalex-snapshot

Synthesis, Biological Evaluation, and Molecular Modeling Studies of New 1,3,4‐Thiadiazole Derivatives as Potent Antimicrobial Agents

inferred← citeshttps://doi.org/10.1002/cbdv.202300611openalex-snapshot

Synthesis and Characterization of Novel 1,3‐Diaryltriazene‐Substituted Sulfaguanidine Derivatives as Selective Carbonic Anhydrase Inhibitors: Biological Evaluation, in Silico ADME/T and Molecular Docking Study

inferred← citeshttps://doi.org/10.1002/cbdv.202301132openalex-snapshot

Biological Effects and Crystal X‐Ray Study of Novel Schiff Base Containing Pentafluorophenyl Hydrazine: In Vitro and in Silico Studies

inferred← citeshttps://doi.org/10.1002/cbdv.202301824openalex-snapshot

Design and Synthesis of Pyrazole Carboxamide Derivatives as Selective Cholinesterase and Carbonic Anhydrase Inhibitors: Molecular Docking and Biological Evaluation

inferred← citeshttps://doi.org/10.1002/cbdv.202401225openalex-snapshot

Inhibition Effects of Some Non‐Proteinogenic Amino Acid Derivatives on Carbonic Anhydrase Isoenzymes and Acetylcholinesterase: An In Vitro Inhibition and Molecular Modeling Studies

inferred← citeshttps://doi.org/10.1002/cbdv.202401849openalex-snapshot

New Sulfonate Ester‐Linked Fluorinated Hydrazone Derivatives as Multitarget Carbonic Anhydrase and Cholinesterase Inhibitors: Design, Synthesis, Biological Evaluation, Molecular Docking and ADME Analysis

inferred← citeshttps://doi.org/10.1002/cbdv.202402893openalex-snapshot

Novel Schiff Base Sulfonate Derivatives as Carbonic Anhydrase and Acetylcholinesterase Inhibitors: Synthesis, Biological Activity, and Molecular Docking Insights

inferred← citeshttps://doi.org/10.1002/cbdv.202403435openalex-snapshot

Synthesis and Carbonic Anhydrase Inhibition Profiles of N‐(3‐sulfamoylphenyl)propanamide/benzamide Derivatives: Experimental and Computational Insights With Absorption, Distribution, Metabolism, and Excretion Profiling

inferred← citeshttps://doi.org/10.1002/cbdv.202501800openalex-snapshot

Exploration of Novel 4‐substituted Coumarin Derivatives as Selective Human Carbonic Anhydrase IX and XII Inhibitors: Synthesis, Biological Evaluation, and In Silico Studies

inferred← citeshttps://doi.org/10.1002/cbic.200800704openalex-snapshot

On‐Chip Fragment‐Based Approach for Discovery of High‐Affinity Bivalent Inhibitors

inferred← citeshttps://doi.org/10.1002/cbic.201600513openalex-snapshot

Structure–Activity Relationships of Benzenesulfonamide‐Based Inhibitors towards Carbonic Anhydrase Isoform Specificity

inferred← citeshttps://doi.org/10.1002/cbic.201600598openalex-snapshot

Characterisation of Photoaffinity‐Based Chemical Probes by Fluorescence Imaging and Native‐State Mass Spectrometry

inferred← citeshttps://doi.org/10.1002/cbic.201800766openalex-snapshot

Quantitative Assessment of Affinity Selection Performance by Using DNA‐Encoded Chemical Libraries

inferred← citeshttps://doi.org/10.1002/cbic.202000387openalex-snapshot

The “Carbonyl Story” and Beyond; Experiences, Lessons and Implications

inferred← citeshttps://doi.org/10.1002/cbic.70519openalex-snapshot

Proton Transport as a Missing Design Variable in Immobilized Enzyme Catalysis

inferred← citeshttps://doi.org/10.1002/cem.2574openalex-snapshot

3D CoMFA, CoMSIA, topomer CoMFA and HQSAR studies on aromatic acid esters for carbonic anhydrase inhibitory activity

inferred← citeshttps://doi.org/10.1002/cem.2579openalex-snapshot

Ligand‐based design, virtual screening, and ADME/T‐based profiling on a dataset of 1,3,5‐triazine‐substituted benzene sulfonamides as carbonic anhydrase inhibitors

inferred← citeshttps://doi.org/10.1002/chem.201200952openalex-snapshot

Discovery of Small‐Molecule Interleukin‐2 Inhibitors from a DNA‐Encoded Chemical Library

inferred← citeshttps://doi.org/10.1002/chem.201500971openalex-snapshot

Orchestrating the Biosynthesis of an Unnatural Pyrrolysine Amino Acid for Its Direct Incorporation into Proteins Inside Living Cells

inferred← citeshttps://doi.org/10.1002/chem.201501037openalex-snapshot

Fluorescent Silica Nanoparticles with Multivalent Inhibitory Effects towards Carbonic Anhydrases

inferred← citeshttps://doi.org/10.1002/chem.201503748openalex-snapshot

A Combined Crystallographic and Theoretical Study Explains the Capability of Carboxylic Acids to Adopt Multiple Binding Modes in the Active Site of Carbonic Anhydrases

inferred← citeshttps://doi.org/10.1002/chem.201504355openalex-snapshot

A Divalent PAMAM‐Based Matrix Metalloproteinase/Carbonic Anhydrase Inhibitor for the Treatment of Dry Eye Syndrome

inferred← citeshttps://doi.org/10.1002/chem.201800941openalex-snapshot

Deciphering the Mechanism of Human Carbonic Anhydrases Inhibition with Sulfocoumarins: Computational and Experimental Studies

inferred← citeshttps://doi.org/10.1002/chem.201805039openalex-snapshot

Phosphorus versus Sulfur: Discovery of Benzenephosphonamidates as Versatile Sulfonamide‐Mimic Chemotypes Acting as Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/chem.202005423openalex-snapshot

A DNA‐Encoded Chemical Library Based on Peptide Macrocycles

inferred← citeshttps://doi.org/10.1002/chem.202103527openalex-snapshot

Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases Inhibition

inferred← citeshttps://doi.org/10.1002/cjoc.202200790openalex-snapshot

Single‐Molecule Measurement of Carbonic Anhydrase in Cation Coordinated Environment Using MspA Nanopore†

inferred← citeshttps://doi.org/10.1002/cjoc.202300736openalex-snapshot

Artificial Water Channel Promoting Depolymerization of Actin Filaments to Trigger Cancer Cell Apoptosis

inferred← citeshttps://doi.org/10.1002/cmdc.200800267openalex-snapshot

Carbonic Anhydrase Inhibitors: Design of Membrane‐Impermeant Copper(II) Complexes of DTPA‐, DOTA‐, and TETA‐Tailed Sulfonamides Targeting the Tumor‐Associated Transmembrane Isoform IX

inferred← citeshttps://doi.org/10.1002/cmdc.201000044openalex-snapshot

Identification of Potent and Selective Human Carbonic Anhydrase VII (hCA VII) Inhibitors

inferred← citeshttps://doi.org/10.1002/cmdc.201000200openalex-snapshot

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

inferred← citeshttps://doi.org/10.1002/cmdc.201000331openalex-snapshot

The X‐ray Structure of the Adduct between NAMI‐A and Carbonic Anhydrase Provides Insights into the Reactivity of this Metallodrug with Proteins

inferred← citeshttps://doi.org/10.1002/cmdc.201200466openalex-snapshot

From In Situ to In Vivo: An In Situ Click‐Chemistry‐Derived Carbonic Anhydrase II Imaging Agent for Positron Emission Tomography

inferred← citeshttps://doi.org/10.1002/cmdc.201402490openalex-snapshot

Functionalization of Fluorinated Benzenesulfonamides and Their Inhibitory Properties toward Carbonic Anhydrases

inferred← citeshttps://doi.org/10.1002/cmdc.201500293openalex-snapshot

Investigating the Selectivity of Metalloenzyme Inhibitors in the Presence of Competing Metalloproteins

inferred← citeshttps://doi.org/10.1002/cmdc.201500596openalex-snapshot

In Vivo Evaluation of Selective Carbonic Anhydrase Inhibitors as Potential Anticonvulsant Agents

inferred← citeshttps://doi.org/10.1002/cmdc.201600180openalex-snapshot

Discovery of New Potential Anti‐Infective Compounds Based on Carbonic Anhydrase Inhibitors by Rational Target‐Focused Repurposing Approaches

inferred← citeshttps://doi.org/10.1002/cmdc.201600204openalex-snapshot

Indazole, Pyrazole, and Oxazole Derivatives Targeting Nitric Oxide Synthases and Carbonic Anhydrases

inferred← citeshttps://doi.org/10.1002/cmdc.201600509openalex-snapshot

Intrinsic Thermodynamics and Structures of 2,4‐ and 3,4‐Substituted Fluorinated Benzenesulfonamides Binding to Carbonic Anhydrases

inferred← citeshttps://doi.org/10.1002/cmdc.201700446openalex-snapshot

Sulfocoumarin‐, Coumarin‐, 4‐Sulfamoylphenyl‐Bearing Indazole‐3‐carboxamide Hybrids: Synthesis and Selective Inhibition of Tumor‐Associated Carbonic Anhydrase Isozymes IX and XII

inferred← citeshttps://doi.org/10.1002/cmdc.201800015openalex-snapshot

Natural Polyphenols Selectively Inhibit β‐Carbonic Anhydrase from the Dandruff‐Producing Fungus Malassezia globosa: Activity and Modeling Studies

inferred← citeshttps://doi.org/10.1002/cmdc.201800180openalex-snapshot

Synthesis and Biological Evaluation of 4‐Sulfamoylphenyl/Sulfocoumarin Carboxamides as Selective Inhibitors of Carbonic Anhydrase Isoforms hCA II, IX, and XII

inferred← citeshttps://doi.org/10.1002/cmdc.201800193openalex-snapshot

A DNA‐Encoded Library of Chemical Compounds Based on Common Scaffolding Structures Reveals the Impact of Ligand Geometry on Protein Recognition

inferred← citeshttps://doi.org/10.1002/cmdc.202000500openalex-snapshot

Synthesis, Computational Studies and Assessment of in Vitro Activity of Squalene Derivatives as Carbonic Anhydrase Inhibitors

inferred← citeshttps://doi.org/10.1002/cmdc.202100510openalex-snapshot

4‐Sulfamoylphenylalkylamides as Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae

inferred← citeshttps://doi.org/10.1002/cmdc.202100725openalex-snapshot

Ureidosulfocoumarin Derivatives As Selective and Potent Carbonic Anhydrase IX and XII Inhibitors

inferred← citeshttps://doi.org/10.1002/cmdc.202200056openalex-snapshot

A Series of Thiadiazolyl‐Benzenesulfonamides Incorporating an Aromatic Tail as Isoform‐Selective, Potent Carbonic Anhydrase II/XII Inhibitors

inferred← citeshttps://doi.org/10.1002/cmdc.202200085openalex-snapshot

Selenocarbamates As a Prodrug‐Based Approach to Carbonic Anhydrase Inhibition

inferred← citeshttps://doi.org/10.1002/cmdc.202200607openalex-snapshot

Versatile Diazomethane Sulfonamide for Expedited Exploration of Azole‐Based Carbonic Anhydrase Inhibitors via [3+2] Cycloaddition

inferred← citeshttps://doi.org/10.1002/cmdc.202200658openalex-snapshot

Inhibition Studies on Carbonic Anhydrase Isoforms I, II, IX, and XII with a Series of Sulfaguanidines

inferred← citeshttps://doi.org/10.1002/cmdc.202300267openalex-snapshot

Antimalarial Agents Targeting Plasmodium falciparum Carbonic Anhydrase: Towards Artesunate Hybrid Compounds with Dual Mechanism of Action

inferred← citeshttps://doi.org/10.1002/cmdc.202300626openalex-snapshot

Exploring the potency of diazo‐coumarin containing hybrid molecules: Selective inhibition of tumor‐associated carbonic anhydrase isoforms IX and XII

inferred← citeshttps://doi.org/10.1002/cmdc.202300680openalex-snapshot

Effective Anticancer Potential of a New Sulfonamide as a Carbonic Anhydrase IX Inhibitor Against Aggressive Tumors

inferred← citeshttps://doi.org/10.1002/cmdc.202400147openalex-snapshot

Phthalazine Sulfonamide Derivatives as Carbonic Anhydrase Inhibitors. Synthesis, Biological and in silico Evaluation

inferred← citeshttps://doi.org/10.1002/cmdc.202400213openalex-snapshot

Aniquinazoline B, a Fungal Natural Product, Activates the μ‐Opioid Receptor

inferred← citeshttps://doi.org/10.1002/cmdc.202400345openalex-snapshot

Thia‐ and Seleno‐Michael Reactions for the Synthesis of Carbonic Anhydrases Inhibitors

inferred← citeshttps://doi.org/10.1002/cmdc.202500080openalex-snapshot

Exploration of 3‐Substituted Benzofuran‐Tethered Sulfamoyl Triazoles as Carbonic Anhydrase Inhibitors: Design, Synthesis, and Biological Evaluation

inferred← citeshttps://doi.org/10.1002/cmdc.202501080openalex-snapshot

Direct‐to‐Biology: Streamlining the Path From Chemistry to Biology in Drug Discovery

inferred← citeshttps://doi.org/10.1002/cmdc.70272openalex-snapshot

A New Series of Amino Alcohol Oxime Ethers as Activators of Human Brain Carbonic Anhydrases: Advances in Selective Activation of Human Carbonic Anhydrase VII

inferred← citeshttps://doi.org/10.1002/cmdc.70369openalex-snapshot

Investigating the Inhibitory Properties of Diazo and Pyrazole‐Carboxamide‐Linked Benzenesulfonamides Against Carbonic Anhydrase Isoforms I, II, IX, and XII

inferred← citeshttps://doi.org/10.1002/cmdc.70379openalex-snapshot

Furagin Derivatives—Nitrofuran‐Based Hydrazones as Potential Dual Inhibitors of Thioredoxin Reductase and Carbonic Anhydrases

inferred← citeshttps://doi.org/10.1002/cmdc.70391openalex-snapshot

Novel Inhibitors of Carbonic Anhydrase I and II Identified by High Throughput Virtual Screening and Validated by X‐Ray Crystallography

inferred← citeshttps://doi.org/10.1002/cmdc.70467openalex-snapshot

Synthesis, Moleculer Modeling, and Carbonic Anhydrase Inhibitor Effects of Novel 1‐(1‐benzyl‐2‐oxoindolin‐3‐ylidene)‐4‐(3‐sulfamoylphenyl)thiosemicarbazides

inferred← citeshttps://doi.org/10.1002/cpdd.47openalex-snapshot

GCG100649, A Novel Cyclooxygenase‐2 Inhibitor, Exhibits a Drug Disposition Profile in Healthy Volunteers Compatible With High Affinity to Carbonic Anhydrase‐I/II: Preliminary Dose–Exposure Relationships to Define Clinical Development Strategies

inferred← citeshttps://doi.org/10.1002/cphc.201701104openalex-snapshot

Ranking Power of the SQM/COSMO Scoring Function on Carbonic Anhydrase II–Inhibitor Complexes

inferred← citeshttps://doi.org/10.1002/cplu.201800194openalex-snapshot

Organoruthenium and Organoosmium Complexes of 2‐Pyridinecarbothioamides Functionalized with a Sulfonamide Motif: Synthesis, Cytotoxicity and Biomolecule Interactions

inferred← citeshttps://doi.org/10.1002/ddr.20262openalex-snapshot

Carbonic anhydrase inhibitors: possible anticancer drugs with a novel mechanism of action

inferred← citeshttps://doi.org/10.1002/ddr.21464openalex-snapshot

Synthesis, carbonic anhydrase inhibitory activity and antioxidant activity of some 1,3‐oxazine derivatives

inferred← citeshttps://doi.org/10.1002/ddr.21906openalex-snapshot

Synthesis of novel hybrid pharmacophore of N ‐(( 4‐sulfamoylphenyl )carbamothioyl)alkanamides as potent carbonic anhydrase‐II and 15‐lipoxygenase inhibitors

inferred← citeshttps://doi.org/10.1002/ddr.21957openalex-snapshot

Click chemistry‐based synthesis of new benzenesulfonamide derivatives bearing triazole ring as selective carbonic anhydrase II inhibitors

inferred← citeshttps://doi.org/10.1002/ddr.22049openalex-snapshot

Selective carbonic anhydrase IX and XII inhibitors based around a functionalized coumarin scaffold

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