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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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Is cyanate a carbonic anhydrase substracte?
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Inhibitory effects of curcumin on tumorigenesis in mice
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Optimization of Xenon Biosensors for Detection of Protein Interactions
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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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Carbonic Anhydrase Inhibitors: Binding of Indanesulfonamides to the Human Isoform II
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Thermodynamic Optimisation in Drug Discovery: A Case Study using Carbonic Anhydrase Inhibitors
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Bidentate Zinc Chelators for α‐Carbonic Anhydrases that Produce a Trigonal Bipyramidal Coordination Geometry
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Functional lung imaging using hyperpolarized gas MRI
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Carbonic Anhydrase Inhibitors. V: Pyrylium Salts in the Synthesis of Isozyme-Specific Inhibitors
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Carbonic Anhydrase Activators. 3: Structure-Activity Correlations for a Series of Isozyme I1 Activators
inferredcites →https://doi.org/10.1002/med.20112openalex-snapshot
Carbonic anhydrase IX: A new druggable target for the design of antitumor agents
inferredcites →https://doi.org/10.1002/med.20141openalex-snapshot
Therapeutic applications of glycosidic carbonic anhydrase inhibitors
inferredcites →https://doi.org/10.1002/pro.5560030115openalex-snapshot
Positions of His‐64 and a bound water in human carbonic anhydrase II upon binding three structurally related inhibitors
inferredcites →https://doi.org/10.1002/pro.5560071201openalex-snapshot
Structural analysis of inhibitor binding to human carbonic anhydrase II
inferredcites →https://doi.org/10.1002/prot.22144openalex-snapshot
Crystal structure of human carbonic anhydrase XIII and its complex with the inhibitor acetazolamide
inferredcites →https://doi.org/10.1002/prot.340040406openalex-snapshot
Refined structure of human carbonic anhydrase II at 2.0 Å resolution
inferredcites →https://doi.org/10.1002/prot.340040407openalex-snapshot
Crystallographic studies of inhibitor binding sites in human carbonic anhydrase II: A pentacoordinated binding of the SCN− ion to the zinc at high pH
inferredcites →https://doi.org/10.1002/prot.340160104openalex-snapshot
Refined structure of bovine carbonic anhydrase III at 2.0 Å resolution
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The efficacy ofSilybum marianum (L.) Gaertn. (silymarin) in the treatment of type II diabetes: a randomized, double-blind, placebo-controlled, clinical trial
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Membrane Carbonic Anhydrase (IV) and Ciliary Epithelium. Carbonic Anhydrase Activity is Present in the Basolateral Membranes of the Non-pigmented Ciliary Epithelium of Rabbit Eyes
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Generation and characterization of the first inhibitory antibody targeting tumour-associated carbonic anhydrase XII
inferredcites →https://doi.org/10.1007/s00726-006-0379-xopenalex-snapshot
Comparison of in vitro antioxidant and antiradical activities of L-tyrosine and L-Dopa
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Carbonic anhydrase catalyzes cyanamide hydration to urea: is it mimicking the physiological reaction?
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Efficacy of three potent steroid sulfatase inhibitors: pre-clinical investigations for their use in the treatment of hormone-dependent breast cancer
inferredcites →https://doi.org/10.1007/s11030-010-9271-4openalex-snapshot
Carbonic anhydrase inhibition with natural products: novel chemotypes and inhibition mechanisms
inferredcites →https://doi.org/10.1007/s11046-007-9020-0openalex-snapshot
In vitro susceptibility to fungicides by invertebrate-pathogenic and saprobic fungi
inferredcites →https://doi.org/10.1016/0005-2795(70)90020-6openalex-snapshot
Sulphonamide complexes of human carbonic anhydrases ultraviolet difference spectroscopy
inferredcites →https://doi.org/10.1016/0014-5793(93)81565-hopenalex-snapshot
The structure of human carbonic anhydrase II in complex with bromide and azide
inferredcites →https://doi.org/10.1016/0014-5793(94)00798-5openalex-snapshot
The structure of a complex between carbonic anhydrase II and a new inhibitor, trifluoromethane sulphonamide
inferredcites →https://doi.org/10.1016/0022-2836(90)90333-hopenalex-snapshot
Insights into the function of the zinc hydroxide-Thr199-Glu106 hydrogen bonding network in carbonic anhydrases
inferredcites →https://doi.org/10.1016/0022-2836(92)90531-nopenalex-snapshot
Structure of native and apo carbonic anhydrase II and structure of some of its anion-ligand complexes
inferredcites →https://doi.org/10.1016/0024-3205(96)00379-7openalex-snapshot
Anticonvulsant activity of topiramate and phenytoin in a rat model of ischemia-induced epilepsy
inferredcites →https://doi.org/10.1016/0042-6822(92)90464-zopenalex-snapshot
A novel quasi-viral agent, MaTu, is a two-component system
inferredcites →https://doi.org/10.1016/0141-8130(90)90040-hopenalex-snapshot
Refined structure of the acetazolamide complex of human carbonic anhydrase II at 1.9 Å
inferredcites →https://doi.org/10.1016/0167-4838(85)90189-xopenalex-snapshot
The inhibition of human carbonic anhydrase II by some organic compounds
inferredcites →https://doi.org/10.1016/0223-5234(96)89133-1openalex-snapshot
5-Substituted 3-thiophenesulfonamides as carbonic anhydrase inhibitors
inferredcites →https://doi.org/10.1016/0960-0760(95)00214-6openalex-snapshot
Sulfamates of various estrogens are prodrugs with increased systemic and reduced hepatic estrogenicity at oral application
inferredcites →https://doi.org/10.1016/j.amjhyper.2007.04.013openalex-snapshot
From Macrocirculation to Microcirculation: Benefits of Preterax
inferredcites →https://doi.org/10.1016/j.bbapap.2009.07.025openalex-snapshot
Sequestration of carbon dioxide by the hydrophobic pocket of the carbonic anhydrases
inferredcites →https://doi.org/10.1016/j.bbapap.2009.07.027openalex-snapshot
Carbonic anhydrase IX: Biochemical and crystallographic characterization of a novel antitumor target
inferredcites →https://doi.org/10.1016/j.bbapap.2009.08.026openalex-snapshot
The γ class of carbonic anhydrases
inferredcites →https://doi.org/10.1016/j.bbrc.2012.02.038openalex-snapshot
Crystal structure of the secretory isozyme of mammalian carbonic anhydrases CA VI: Implications for biological assembly and inhibitor development
inferredcites →https://doi.org/10.1016/j.bmc.2007.03.070openalex-snapshot
Molecular modeling study for the binding of zonisamide and topiramate to the human mitochondrial carbonic anhydrase isoform VA
inferredcites →https://doi.org/10.1016/j.bmc.2007.04.020openalex-snapshot
Carbonic anhydrases as targets for medicinal chemistry
inferredcites →https://doi.org/10.1016/j.bmc.2008.06.013openalex-snapshot
Carbonic anhydrase inhibitors: Inhibition of mammalian isoforms I–XIV with a series of substituted phenols including paracetamol and salicylic acid
inferredcites →https://doi.org/10.1016/j.bmc.2008.08.043openalex-snapshot
Carbonic anhydrase activators: Kinetic and X-ray crystallographic study for the interaction of d- and l-tryptophan with the mammalian isoforms I–XIV
inferredcites →https://doi.org/10.1016/j.bmc.2008.09.032openalex-snapshot
Carbonic anhydrase inhibitors: Synthesis and inhibition studies against mammalian isoforms I–XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides
inferredcites →https://doi.org/10.1016/j.bmc.2008.12.023openalex-snapshot
Carbonic anhydrase inhibitors. Comparison of chlorthalidone, indapamide, trichloromethiazide, and furosemide X-ray crystal structures in adducts with isozyme II, when several water molecules make the difference
inferredcites →https://doi.org/10.1016/j.bmc.2009.03.066openalex-snapshot
Synthesis and evaluation of pharmacological profile of 1-aryl-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-sulfonamides
inferredcites →https://doi.org/10.1016/j.bmc.2009.11.021openalex-snapshot
Carbonic anhydrase inhibitors. Identification of selective inhibitors of the human mitochondrial isozymes VA and VB over the cytosolic isozymes I and II from a natural product-based phenolic library
inferredcites →https://doi.org/10.1016/j.bmc.2010.01.076openalex-snapshot
Carbonic anhydrase inhibitors. Inhibition of mammalian isoforms I–XIV with a series of natural product polyphenols and phenolic acids
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
inferredcites →https://doi.org/10.1016/j.bmcl.2003.09.063openalex-snapshot
Carbonic anhydrase inhibitors: N-(p-sulfamoylphenyl)-α-d-glycopyranosylamines as topically acting antiglaucoma agents in hypertensive rabbits
inferredcites →https://doi.org/10.1016/j.bmcl.2003.09.064openalex-snapshot
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.2003.12.029openalex-snapshot
Carbonic anhydrase inhibitors: The first selective, membrane-impermeant inhibitors targeting the tumor-associated isozyme IX
inferredcites →https://doi.org/10.1016/j.bmcl.2004.01.096openalex-snapshot
Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with a topically acting antiglaucoma sulfonamide
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.2004.11.058openalex-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.2005.01.086openalex-snapshot
Carbonic anhydrase inhibitors: X-ray crystal structure of a benzenesulfonamide strong CA II and CA IX inhibitor bearing a pentafluorophenylaminothioureido tail in complex with isozyme II
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.2005.08.069openalex-snapshot
Carbonic anhydrase activators: X-ray crystal structure of the adduct of human isozyme II with l-histidine as a platform for the design of stronger activators
inferredcites →https://doi.org/10.1016/j.bmcl.2006.05.068openalex-snapshot
N-Hydroxyurea—A versatile zinc binding function in the design of metalloenzyme inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2006.06.064openalex-snapshot
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.2006.09.022openalex-snapshot
Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of 5-amino-1,3,4-thiadiazole-2-sulfonamide and 5-(4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide to human isoform II
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
inferredcites →https://doi.org/10.1016/j.bmcl.2006.11.046openalex-snapshot
Inhibition of membrane-associated carbonic anhydrase isozymes IX, XII and XIV with a library of glycoconjugate benzenesulfonamides
inferredcites →https://doi.org/10.1016/j.bmcl.2006.12.099openalex-snapshot
Carbonic anhydrase inhibitors: Binding of an antiglaucoma glycosyl-sulfanilamide derivative to human isoform II and its consequences for the drug design of enzyme inhibitors incorporating sugar moieties
inferredcites →https://doi.org/10.1016/j.bmcl.2007.05.045openalex-snapshot
Carbonic anhydrase inhibitors: Inhibition of human, bacterial, and archaeal isozymes with benzene-1,3-disulfonamides—Solution and crystallographic studies
inferredcites →https://doi.org/10.1016/j.bmcl.2007.07.023openalex-snapshot
Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I and II, and extracellular isoforms IV, IX, and XII with sulfamides incorporating sugar moieties
inferredcites →https://doi.org/10.1016/j.bmcl.2007.10.110openalex-snapshot
Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide with 12 mammalian isoforms: Kinetic and X-ray crystallographic studies
inferredcites →https://doi.org/10.1016/j.bmcl.2007.12.022openalex-snapshot
Carbonic anhydrase inhibitors. Interaction of 2-N,N-dimethylamino-1,3,4-thiadiazole-5-methanesulfonamide with 12 mammalian isoforms: Kinetic and X-ray crystallographic studies
inferredcites →https://doi.org/10.1016/j.bmcl.2008.01.077openalex-snapshot
Carbonic anhydrase inhibitors: Interactions of phenols with the 12 catalytically active mammalian isoforms (CA I–XIV)
inferredcites →https://doi.org/10.1016/j.bmcl.2008.03.012openalex-snapshot
Investigations of the esterase, phosphatase, and sulfatase activities of the cytosolic mammalian carbonic anhydrase isoforms I, II, and XIII with 4-nitrophenyl esters as substrates
inferredcites →https://doi.org/10.1016/j.bmcl.2008.03.051openalex-snapshot
Carbonic anhydrase inhibitors. Interaction of indapamide and related diuretics with 12 mammalian isozymes and X-ray crystallographic studies for the indapamide–isozyme II adduct
inferredcites →https://doi.org/10.1016/j.bmcl.2008.05.051openalex-snapshot
Carbonic anhydrase inhibitors: Design of spin-labeled sulfonamides incorporating TEMPO moieties as probes for cytosolic or transmembrane isozymes
inferredcites →https://doi.org/10.1016/j.bmcl.2009.01.038openalex-snapshot
A thiabendazole sulfonamide shows potent inhibitory activity against mammalian and nematode α-carbonic anhydrases
inferredcites →https://doi.org/10.1016/j.bmcl.2009.04.123openalex-snapshot
Carbonic anhydrase inhibitors. Phenacetyl-, pyridylacetyl- and thienylacetyl-substituted aromatic sulfonamides act as potent and selective isoform VII inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2009.10.036openalex-snapshot
Nitric oxide-donating carbonic anhydrase inhibitors for the treatment of open-angle glaucoma
inferredcites →https://doi.org/10.1016/j.bmcl.2009.11.124openalex-snapshot
Carbonic anhydrase inhibitors. X-ray crystal studies of the carbonic anhydrase II–trithiocarbonate adduct—An inhibitor mimicking the sulfonamide and urea binding to the enzyme
inferredcites →https://doi.org/10.1016/j.bmcl.2010.06.040openalex-snapshot
Coumarins incorporating hydroxy- and chloro-moieties selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and II
inferredcites →https://doi.org/10.1016/j.bmcl.2010.07.038openalex-snapshot
Carbonic anhydrase inhibitors. Antioxidant polyphenols effectively inhibit mammalian isoforms I–XV
inferredcites →https://doi.org/10.1016/j.bmcl.2010.07.051openalex-snapshot
Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamide
inferredcites →https://doi.org/10.1016/j.bmcl.2010.10.094openalex-snapshot
7,8-Disubstituted- but not 6,7-disubstituted coumarins selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and II in the low nanomolar/subnanomolar range
inferredcites →https://doi.org/10.1016/j.bmcl.2011.01.050openalex-snapshot
(R)-/(S)-10-Camphorsulfonyl-substituted aromatic/heterocyclic sulfonamides selectively inhibit mitochondrial over cytosolic carbonic anhydrases
inferredcites →https://doi.org/10.1016/j.cbi.2008.05.003openalex-snapshot
Antioxidant and radical scavenging properties of curcumin
inferredcites →https://doi.org/10.1016/j.exer.2005.03.010openalex-snapshot
Carbonic anhydrase XIV identified as the membrane CA in mouse retina: strong expression in Müller cells and the RPE
inferredcites →https://doi.org/10.1016/j.fct.2010.05.053openalex-snapshot
Polyphenol contents and antioxidant activity of lyophilized aqueous extract of propolis from Erzurum, Turkey
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.freeradbiomed.2006.10.054openalex-snapshot
NOX5 variants are functionally active in endothelial cells
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Acetazolamide and midazolam act synergistically to inhibit neuropathic pain
inferredcites →https://doi.org/10.1016/j.tox.2005.09.011openalex-snapshot
Antioxidant activity of caffeic acid (3,4-dihydroxycinnamic acid)
inferredcites →https://doi.org/10.1016/s0006-291x(82)80063-6openalex-snapshot
Phenol, a competitive inhibitor of CO2 hydration catalyzed by carbonic anhydrase
inferredcites →https://doi.org/10.1016/s0021-9258(18)95800-xopenalex-snapshot
Esterase Activities of Human Carbonic Anhydrases B and C
inferredcites →https://doi.org/10.1016/s0021-9258(19)45714-1openalex-snapshot
Electron Spin Resonance Studies of Spin-labeled Carbonic Anhydrase
inferredcites →https://doi.org/10.1016/s0021-9258(19)47376-6openalex-snapshot
Altering the mouth of a hydrophobic pocket. Structure and kinetics of human carbonic anhydrase II mutants at residue Val-121.
inferredcites →https://doi.org/10.1016/s0021-9258(19)51331-xopenalex-snapshot
THE INHIBITION OF CARBONIC ANHYDRASE BY THIOPHENE-2-SULFONAMIDE AND SULFANILAMIDE
inferredcites →https://doi.org/10.1016/s0021-9258(19)74305-1openalex-snapshot
A new class of carbonic anhydrase inhibitor.
inferredcites →https://doi.org/10.1016/s0022-3565(25)11469-9openalex-snapshot
Nitrovasodilators as a new class of ocular hypotensive agents.
inferredcites →https://doi.org/10.1016/s0026-895x(25)10806-7openalex-snapshot
A Comparative Study of Mammalian Erythrocyte Carbonic Anhydrases Employing Spin-Labeled Analogues of Inhibitory Sulfonamides
inferredcites →https://doi.org/10.1016/s0026-895x(25)13717-6openalex-snapshot
A Spin Label Study of Human Erythrocyte Carbonic Anhydrases B and C
inferredcites →https://doi.org/10.1016/s0039-6257(97)84043-xopenalex-snapshot
Nitric oxide in the eye: Multifaceted roles and diverse outcomes
inferredcites →https://doi.org/10.1016/s0065-2423(06)42005-9openalex-snapshot
Tumor‐associated Carbonic Anhydrases and Their Clinical Significance
inferredcites →https://doi.org/10.1016/s0076-6879(07)35022-2openalex-snapshot
Superoxide and Derived Reactive Oxygen Species in the Regulation of Hypoxia‐Inducible Factors
inferredcites →https://doi.org/10.1016/s0079-6565(02)00052-3openalex-snapshot
Hyperpolarised xenon in biology
inferredcites →https://doi.org/10.1016/s0140-6736(07)61303-8openalex-snapshot
Effects of a fixed combination of perindopril and indapamide on macrovascular and microvascular outcomes in patients with type 2 diabetes mellitus (the ADVANCE trial): a randomised controlled trial
inferredcites →https://doi.org/10.1016/s0163-7258(96)00198-2openalex-snapshot
Structure and mechanism of carbonic anhydrase
inferredcites →https://doi.org/10.1016/s0223-5234(97)86179-xopenalex-snapshot
Carbonic anhydrase inhibitors. Part 37. Novel classes of isozyme I and II inhibitors and their mechanism of action. Kinetic and spectroscopic investigations on native and cobalt-substituted enzymes
inferredcites →https://doi.org/10.1016/s0223-5234(98)80017-2openalex-snapshot
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
inferredcites →https://doi.org/10.1016/s0223-5234(98)80033-0openalex-snapshot
Carbonic anhydrase inhibitors - Part 49: Synthesis of substituted ureido and thioureido derivatives of aromatic/heterocyclic sulfonamides with increased affinities for isozyme I
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/s0920-1211(00)00118-2openalex-snapshot
A comparison of topiramate and acetazolamide on seizure duration and paired-pulse inhibition in the dentate gyrus of the rat
inferredcites →https://doi.org/10.1016/s0920-1211(00)00171-6openalex-snapshot
Progress report on new antiepileptic drugs: a summary of the Fifth Eilat Conference (EILAT V)
inferredcites →https://doi.org/10.1016/s0960-0760(03)00048-7openalex-snapshot
Novel D-ring modified steroid derivatives as potent, non-estrogenic, steroid sulfatase inhibitors with in vivo activity
inferredcites →https://doi.org/10.1016/s0960-894x(01)00303-1openalex-snapshot
Carbonic anhydrase inhibitors: 4-sulfamoyl-benzenecarboxamides and 4-chloro-3-sulfamoyl-benzenecarboxamides with strong topical antiglaucoma properties
inferredcites →https://doi.org/10.1016/s0960-894x(03)00029-5openalex-snapshot
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)00508-0openalex-snapshot
Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with a bis-sulfonamide—two heads are better than one?
inferredcites →https://doi.org/10.1016/s0960-894x(03)00580-8openalex-snapshot
Carbonic anhydrase inhibitors: Topically acting antiglaucoma sulfonamides incorporating esters and amides of 3- and 4-carboxybenzolamide
inferredcites →https://doi.org/10.1016/s0968-0896(03)00042-7openalex-snapshot
D-Ring Modified Estrone Derivatives as Novel Potent Inhibitors of Steroid Sulfatase
inferredcites →https://doi.org/10.1016/s0968-0896(03)00112-3openalex-snapshot
Hydroxyurea is a carbonic anhydrase inhibitor
inferredcites →https://doi.org/10.1017/s0031182097001029openalex-snapshot
Target sites of anthelmintics
inferredcites →https://doi.org/10.1017/s003358350700460xopenalex-snapshot
Long-range distance determinations in biomacromolecules by EPR spectroscopy
inferredcites →https://doi.org/10.1021/ar7000588openalex-snapshot
Solvent-Mediated Proton Transfer in Catalysis by Carbonic Anhydrase
inferredcites →https://doi.org/10.1021/ar9501232openalex-snapshot
Carbonic Anhydrase: Evolution of the Zinc Binding Site by Nature and by Design
inferredcites →https://doi.org/10.1021/bi00068a004openalex-snapshot
Kinetic and spectroscopic studies of hydrophilic amino acid substitutions in the hydrophobic pocket of human carbonic anhydrase II
inferredcites →https://doi.org/10.1021/bi00068a005openalex-snapshot
Structural consequences of hydrophilic amino acid substitutions in the hydrophobic pocket of human carbonic anhydrase II
inferredcites →https://doi.org/10.1021/bi000937copenalex-snapshot
Mechanism of Cyanamide Hydration Catalyzed by Carbonic Anhydrase II Suggested by Cryogenic X-ray Diffraction
inferredcites →https://doi.org/10.1021/bi00110a007openalex-snapshot
Functional consequences of engineering the hydrophobic pocket of carbonic anhydrase II
inferredcites →https://doi.org/10.1021/bi00110a008openalex-snapshot
Engineering the hydrophobic pocket of carbonic anhydrase II
inferredcites →https://doi.org/10.1021/bi00331a010openalex-snapshot
Dynamic carbon-13 NMR investigations of substrate interaction and catalysis by cobalt(II) human carbonic anhydrase I
inferredcites →https://doi.org/10.1021/bi00445a054openalex-snapshot
Role of histidine 64 in the catalytic mechanism of human carbonic anhydrase II studied with a site-specific mutant
inferredcites →https://doi.org/10.1021/bi00845a050openalex-snapshot
The catalytic versatility of erythrocyte carbonic anhydrase. V. Kinetic studies of enzyme-catalyzed hydrations of aliphatic aldehydes
inferredcites →https://doi.org/10.1021/bi00853a037openalex-snapshot
The Catalytic Versatility of Erythrocyte Carbonic Anhydrase. II. Kinetic Studies of the Enzyme-Catalyzed Hydration of Pyridine Aldehydes*
inferredcites →https://doi.org/10.1021/bi00855a005openalex-snapshot
The Catalytic Versatility of Erythrocyte Carbonic Anhydrase. III. Kinetic Studies of the Enzyme-Catalyzed Hydrolysis of p-Nitrophenyl Acetate*
inferredcites →https://doi.org/10.1021/bi047692eopenalex-snapshot
First Crystal Structures of Human Carbonic Anhydrase II in Complex with Dual Aromatase−Steroid Sulfatase Inhibitors,
inferredcites →https://doi.org/10.1021/bi050610hopenalex-snapshot
Human Carbonic Anhydrase III: Structural and Kinetic Study of Catalysis and Proton Transfer,
inferredcites →https://doi.org/10.1021/bi062066yopenalex-snapshot
Atomic Crystal and Molecular Dynamics Simulation Structures of Human Carbonic Anhydrase II: Insights into the Proton Transfer Mechanism,
inferredcites →https://doi.org/10.1021/bi702385kopenalex-snapshot
Inhibition of Carbonic Anhydrase II by Thioxolone: A Mechanistic and Structural Study
inferredcites →https://doi.org/10.1021/bi902178wopenalex-snapshot
Structures of Human Carbonic Anhydrase II/Inhibitor Complexes Reveal a Second Binding Site for Steroidal and Nonsteroidal 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/cr050262popenalex-snapshot
Carbonic Anhydrase as a Model for Biophysical and Physical-Organic Studies of Proteins and Protein−Ligand Binding
inferredcites →https://doi.org/10.1021/ja00002a004openalex-snapshot
Carbon dioxide binding to human carbonic anhydrase II
inferredcites →https://doi.org/10.1021/ja00087a086openalex-snapshot
Two-Site Binding of Phenol in the Active Site of Human Carbonic Anhydrase II: Structural Implications for Substrate Association
inferredcites →https://doi.org/10.1021/ja00091a005openalex-snapshot
Lack of Effect of the Length of Oligoglycine- and Oligo(ethylene glycol)-Derived para-Substituents on the Affinity of Benzenesulfonamides for Carbonic Anhydrase II in Solution
inferredcites →https://doi.org/10.1021/ja00091a006openalex-snapshot
Mapping Protein-Peptide Affinity: Binding of Peptidylsulfonamide Inhibitors to Human Carbonic Anhydrase II
inferredcites →https://doi.org/10.1021/ja00128a001openalex-snapshot
Molecular Dynamics Simulations of H2NSO2C6H4CONH(Gly)3OBn Bound to the Active Site of Human Carbonic Anhydrase II
inferredcites →https://doi.org/10.1021/ja00259a038openalex-snapshot
Interaction of carbon dioxide and copper(II) carbonic anhydrase
inferredcites →https://doi.org/10.1021/ja00753a055openalex-snapshot
Spin label investigation of the active site of an enzyme. Bovine carbonic anhydrase
inferredcites →https://doi.org/10.1021/ja01045a054openalex-snapshot
Carbonic anhydrase catalyzed hydrolysis of 2-hydroxy-5-nitro-.alpha.-toluenesulfonic acid sultone
inferredcites →https://doi.org/10.1021/ja01167a011openalex-snapshot
The Preparation of Heterocyclic Sulfonamides1
inferredcites →https://doi.org/10.1021/ja01167a012openalex-snapshot
Heterocyclic Sulfonamides as Carbonic Anhydrase Inhibitors 1
inferredcites →https://doi.org/10.1021/ja01599a033openalex-snapshot
1,3,4-Thiadiazole- and Thiadiazolinesulfonamides as Carbonic Anhydrase Inhibitors. Synthesis and Structural Studies
inferredcites →https://doi.org/10.1021/ja047271kopenalex-snapshot
Two-Prong Inhibitors for Human Carbonic Anhydrase II
inferredcites →https://doi.org/10.1021/ja047557popenalex-snapshot
Protein Surface-Assisted Enhancement in the Binding Affinity of an Inhibitor for Recombinant Human Carbonic Anhydrase-II
inferredcites →https://doi.org/10.1021/ja057257nopenalex-snapshot
Ultrahigh Resolution Crystal Structures of Human Carbonic Anhydrases I and II Complexed with “Two-Prong” Inhibitors Reveal the Molecular Basis of High Affinity
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/ja068359wopenalex-snapshot
Structural Analysis of Charge Discrimination in the Binding of Inhibitors to Human Carbonic Anhydrases I and II
inferredcites →https://doi.org/10.1021/ja072965popenalex-snapshot
Thermodynamics of Xenon Binding to Cryptophane in Water and Human Plasma
inferredcites →https://doi.org/10.1021/ja802214xopenalex-snapshot
Structure of a 129 Xe-Cryptophane Biosensor Complexed with Human Carbonic Anhydrase II
inferredcites →https://doi.org/10.1021/ja806092wopenalex-snapshot
Cryptophane Xenon-129 Nuclear Magnetic Resonance Biosensors Targeting Human Carbonic Anhydrase
inferredcites →https://doi.org/10.1021/ja809683vopenalex-snapshot
Non-Zinc Mediated Inhibition of Carbonic Anhydrases: Coumarins Are a New Class of Suicide Inhibitors
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Structure-Based Design of a Sulfonamide Probe for Fluorescence Anisotropy Detection of Zinc with a Carbonic Anhydrase-Based Biosensor
inferredcites →https://doi.org/10.1021/ja963832zopenalex-snapshot
Novel Binding Mode of Hydroxamate Inhibitors to Human Carbonic Anhydrase II
inferredcites →https://doi.org/10.1021/jm00013a004openalex-snapshot
Secondary Interactions Significantly Removed from the Sulfonamide Binding Pocket of Carbonic Anhydrase II Influence Inhibitor Binding Constants
inferredcites →https://doi.org/10.1021/jm00013a005openalex-snapshot
Increasing Binding Constants of Ligands to Carbonic Anhydrase by Using "Greasy Tails"
inferredcites →https://doi.org/10.1021/jm00028a002openalex-snapshot
Estrone sulfamates: potent inhibitors of estrone sulfatase with therapeutic potential
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/jm00039a023openalex-snapshot
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
inferredcites →https://doi.org/10.1021/jm00052a017openalex-snapshot
Synthesis and Anticonvulsant Activities of .alpha.-Acetamido-N-benzylacetamide Derivatives Containing an Electron-Deficient .alpha.-Heteroaromatic Substituent
inferredcites →https://doi.org/10.1021/jm00074a016openalex-snapshot
Synthesis and anticonvulsant activities of .alpha.-heterocyclic .alpha.-acetamido-N-benzylacetamide derivatives
inferredcites →https://doi.org/10.1021/jm00104a003openalex-snapshot
Synthesis and physiochemical properties of sulfamate derivatives as topical antiglaucoma agents
inferredcites →https://doi.org/10.1021/jm001051+openalex-snapshot
Carbonic Anhydrase Inhibitors: Water-Soluble 4-Sulfamoylphenylthioureas as Topical Intraocular Pressure-Lowering Agents with Long-Lasting Effects
inferredcites →https://doi.org/10.1021/jm00140a009openalex-snapshot
Cerebrovasodilatation through selective inhibition of the enzyme carbonic anhydrase. 3. 5-(Arylthio)-, 5-(arylsulfinyl)-, and 5-(arylsulfonyl)thiophene-2-sulfonamides
inferredcites →https://doi.org/10.1021/jm00165a006openalex-snapshot
Preparation and anticonvulsant activity of a series of functionalized .alpha.-aromatic and .alpha.-heteroaromatic amino acids
inferredcites →https://doi.org/10.1021/jm00278a034openalex-snapshot
Synthesis of some spin-labeled analogs of drug molecules
inferredcites →https://doi.org/10.1021/jm00386a021openalex-snapshot
Functionalized DL-amino acid derivatives. Potent new agents for the treatment of epilepsy
inferredcites →https://doi.org/10.1021/jm00387a002openalex-snapshot
Thienothiopyran-2-sulfonamides: a novel class of water-soluble carbonic anhydrase inhibitors
inferredcites →https://doi.org/10.1021/jm00388a023openalex-snapshot
Anticonvulsant O-alkyl sulfamates. 2,3:4,5-Bis-O-(1-methylethylidene)-.beta.-D-fructopyranose sulfamate and related compounds
inferredcites →https://doi.org/10.1021/jm010163dopenalex-snapshot
Structural Aspects of Isozyme Selectivity in the Binding of Inhibitors to Carbonic Anhydrases II and IV
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/jm011112jopenalex-snapshot
Successful Virtual Screening for Novel Inhibitors of Human Carbonic Anhydrase: Strategy and Experimental Confirmation
inferredcites →https://doi.org/10.1021/jm011131topenalex-snapshot
Nonaromatic Sulfonamide Group as an Ideal Anchor for Potent Human Carbonic Anhydrase Inhibitors: Role of Hydrogen-Bonding Networks in Ligand Binding and Drug Design
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/jm031079wopenalex-snapshot
Carbonic Anhydrase Inhibitors. Design of Selective, Membrane-Impermeant Inhibitors Targeting the Human Tumor-Associated Isozyme IX
inferredcites →https://doi.org/10.1021/jm031116jopenalex-snapshot
Carbonic Anhydrase Inhibitors: Synthesis and Topical Intraocular Pressure Lowering Effects of Fluorine-Containing Inhibitors Devoid of Enhanced Reactivity
inferredcites →https://doi.org/10.1021/jm034033bopenalex-snapshot
First Dual Aromatase-Steroid Sulfatase Inhibitors
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/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
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Potent inhibitors of tumor associated carbonic anhydrases endowed with cathepsin B inhibition
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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.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.202400601openalex-snapshot
Lasamide Containing Sulfonylpiperazines as Effective Agents for the Management of Glaucoma Associated Symptoms
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.202500633openalex-snapshot
Exploration of New Pyrazole–Hydrazone–Benzenesulfonamide Conjugates as Potent Mycobacterial Carbonic Anhydrase Inhibitors: Design, Synthesis, and Biological Evaluation
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.70353openalex-snapshot
Piperazine Derivatives Carrying an Imidazole Ring as Selective Modulators of Human Carbonic Anhydrase Isozymes
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.70390openalex-snapshot
1‐Aryl‐6,7‐Dimethoxy‐3,4‐Dihydroisoquinoline‐2(1 H )‐Sulfonamides as hCA XII Selective Inhibitors: Experimental and Theoretical Studies to Interrogate the Isoform Selectivity
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.202200770openalex-snapshot
A Case Study on the Use of Binding Free Energies to Screen Inhibitors of Human Carbonic Anhydrase II
inferred← citeshttps://doi.org/10.1002/cphc.202500573openalex-snapshot
Effect of Glycosylation on the Reorganization at the Active Site of Human Carbonic Anhydrase IX
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/cplu.202000574openalex-snapshot
Cobalt Bis(dicarbollide) Alkylsulfonamides: Potent and Highly Selective Inhibitors of Tumor Specific Carbonic Anhydrase IX
inferred← citeshttps://doi.org/10.1002/ddr.22135openalex-snapshot
Novel sulfonamide‐phosphonate conjugates as carbonic anhydrase isozymes inhibitors
inferred← citeshttps://doi.org/10.1002/ddr.70030openalex-snapshot
Design and Discovery of New Dual Carbonic Anhydrase IX and VEGFR‐2 Inhibitors Based on the Benzenesulfonamide‐Bearing 4‐Thiazolidinones/2,4‐Thiazolidinediones Scaffold
inferred← citeshttps://doi.org/10.1002/ejoc.202100250openalex-snapshot
Synthesis of Azasugar–Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity
inferred← citeshttps://doi.org/10.1002/jbt.21788openalex-snapshot
Investigation of the Effect of Some Optically Active Imine Compounds on the Enzyme Activities of hCA‐I and hCA‐II under In Vitro Conditions: An Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1002/jbt.21998openalex-snapshot
Synthesis of 2‐amino‐3‐cyanopyridine derivatives and investigation of their carbonic anhydrase inhibition effects
inferred← citeshttps://doi.org/10.1002/jbt.22041openalex-snapshot
The in vivo effects of cefazolin, cefuroxime, and cefoperazon on the carbonic anhydrase in different rat tissues
inferred← citeshttps://doi.org/10.1002/jbt.22194openalex-snapshot
1H‐indazole molecules reduced the activity of human erythrocytes carbonic anhydrase I and II isoenzymes
inferred← citeshttps://doi.org/10.1002/jbt.22300openalex-snapshot
Investigation of the effects of some sulfonamides on acetylcholinesterase and carbonic anhydrase enzymes
inferred← citeshttps://doi.org/10.1002/jbt.23704openalex-snapshot
Synthesis, molecular docking analysis, drug‐likeness evaluation, and inhibition potency of new pyrazole‐3,4‐dicarboxamides incorporating sulfonamide moiety as carbonic anhydrase inhibitors
inferred← citeshttps://doi.org/10.1002/jbt.23837openalex-snapshot
The synthesis of novel unnatural amino acid by intramolecular aza‐Michael addition reaction as multitarget enzyme inhibitors
inferred← citeshttps://doi.org/10.1002/jbt.70135openalex-snapshot
Design, Synthesis, and In Vitro Evaluation of Aromatic Sulfonamides as Human Carbonic Anhydrase I, II, IX, and XII Inhibitors and Their Antioxidant Activity
inferred← citeshttps://doi.org/10.1002/jbt.70217openalex-snapshot
Investigating the Anti‐Inflammatory Potential of SLC‐0111: A Carbonic Anhydrase Inhibitor Targeting Cyclooxygenase‐Mediated Inflammatory Pathways in a Carrageenan‐Induced Rat Model
inferred← citeshttps://doi.org/10.1002/jbt.70497openalex-snapshot
Green Synthesis of Sulfonamide Derivatives as Human Carbonic Anhydrase Isoforms I, II, IX, XII Inhibitors and Antioxidants: Comprehensive Insights From Biological Evaluation and In‐Depth In Silico Analysis
inferred← citeshttps://doi.org/10.1002/jcc.23998openalex-snapshot
Aqueous acidities of primary benzenesulfonamides: Quantum chemical predictions based on density functional theory and SMD
inferred← citeshttps://doi.org/10.1002/jhet.70138openalex-snapshot
Synthesis of Novel Benzimidazole Derivatives as a Carbonic Anhydrase IX (Ca IX ) Inhibitor With Anticancer Potential
inferred← citeshttps://doi.org/10.1002/jobm.202300323openalex-snapshot
Evolutionary analysis and quality assessment of ζ‐carbonic anhydrase sequences from environmental microbiome
inferred← citeshttps://doi.org/10.1002/med.21497openalex-snapshot
Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of one
inferred← citeshttps://doi.org/10.1002/med.21713openalex-snapshot
Progress in the development of human carbonic anhydrase inhibitors and their pharmacological applications: Where are we today?
inferred← citeshttps://doi.org/10.1002/med.22115openalex-snapshot
Comprehensive Insights Into Sulfanilamido‐Based Medicinal Design and Research
inferred← citeshttps://doi.org/10.1002/prot.26022openalex-snapshot
Molecular dynamics simulations identify the regions of compromised thermostability in SazCA
inferred← citeshttps://doi.org/10.1002/slct.201700531openalex-snapshot
Combinatorial Design of Isoform‐Selective N‐Alkylated Benzimidazole‐Based Inhibitors of Carbonic Anhydrases
inferred← citeshttps://doi.org/10.1002/slct.201802677openalex-snapshot
One‐pot, Four‐Component Green Synthesis, Carbonic Anhydrase II Inhibition and Docking Studies of 5‐Arylidenerhodanines
inferred← citeshttps://doi.org/10.1002/slct.202101854openalex-snapshot
A Practical Method of N ‐Methylpyrrole Disulfonamides Synthesis: Computational Studies, Carbonic Anhydrase Inhibition and Electrochemical DNA Binding Investigations
inferred← citeshttps://doi.org/10.1002/slct.202204578openalex-snapshot
Metal‐Free Synthesis via Intramolecular Cyclization, Enzyme Inhibition Properties and Molecular Docking of Novel Isoindolinones
inferred← citeshttps://doi.org/10.1002/slct.202303236openalex-snapshot
Investigation of the Effects of 1,2,4‐Triazole and Thiazole Ring‐Containing Hybrid Molecules on Carbonic Anhydrase I and II
inferred← citeshttps://doi.org/10.1002/slct.202400684openalex-snapshot
Identification of hCA I, hCA II, AChE and BChE Inhibitory Properties of Some Norcantharimide Derivatives; Molecular Docking, SAR and in silico ADME Studies
inferred← citeshttps://doi.org/10.1002/slct.202501331openalex-snapshot
Synthesis and Characterization of New Ureido‐Containing Benzenesulfonamide Derivatives and Their Inhibition Effects on Carbonic Anhydrase Isoforms I, II, IX, and XII
inferred← citeshttps://doi.org/10.1002/slct.202505428openalex-snapshot
E ‐Stilbene‐Based Hydrazide‐1,3,4‐Oxadiazole Hybrids as Potential Anticancer Dual Carbonic Anhydrase‐I and Thymidine Phosphorylase Inhibitors: In Vitro and In Silico Studies
inferred← citeshttps://doi.org/10.1002/slct.202506256openalex-snapshot
Design and Synthesis of Urea–Sulfonamides as Potential VEGFR‐2 Inhibitors and Apoptosis Inducers in Cancer Therapy
inferred← citeshttps://doi.org/10.1002/smll.202307537openalex-snapshot
Engineering Zinc–Organic Frameworks‐Based Artificial Carbonic Anhydrase with Ultrafast Biomimetic Centers for Efficient Hydration Reactions
inferred← citeshttps://doi.org/10.1007/7081_2014_124openalex-snapshot
Biological Properties of 1H-1,2,3- and 2H-1,2,3-Triazoles
inferred← citeshttps://doi.org/10.1007/7355_2016_10openalex-snapshot
Fungal Carbonic Anhydrases and Their Inhibition
inferred← citeshttps://doi.org/10.1007/7355_2021_138openalex-snapshot
Beta-Carbonic Anhydrase 1 from Trichomonas Vaginalis as New Antiprotozoan Drug Target
inferred← citeshttps://doi.org/10.1007/7355_2021_140openalex-snapshot
Targeting Carbonic Anhydrases from Trypanosoma cruzi and Leishmania spp. as a Therapeutic Strategy to Obtain New Antiprotozoal Drugs
inferred← citeshttps://doi.org/10.1007/978-1-4939-7899-1_12openalex-snapshot
Approaching Pharmacological Space: Events and Components
inferred← citeshttps://doi.org/10.1007/978-3-030-12780-0_18openalex-snapshot
Efficacy of Novel CA IX Inhibitors in Biological Models
inferred← citeshttps://doi.org/10.1007/978-3-030-57456-7_6openalex-snapshot
A Story on Carbon Dioxide and Its Hydration
inferred← citeshttps://doi.org/10.1007/978-3-030-79511-5_10openalex-snapshot
Carbonic Anhydrase Inhibitors: Designing Isozyme-Specific Inhibitors as Therapeutic Agents
inferred← citeshttps://doi.org/10.1007/978-3-030-79511-5_12openalex-snapshot
Targeting Carbonic Anhydrase IX in Tumor Imaging and Theranostic Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-3-642-38111-9_3openalex-snapshot
Hydroxamates as Carbonic Anhydrase Inhibitors
inferred← citeshttps://doi.org/10.1007/978-94-007-7359-2_15openalex-snapshot
Carbonic Anhydrase Inhibitors Drug Design
inferred← citeshttps://doi.org/10.1007/978-94-007-7359-2_17openalex-snapshot
Glaucoma and the Applications of Carbonic Anhydrase Inhibitors
inferred← citeshttps://doi.org/10.1007/978-94-007-7359-2_19openalex-snapshot
Thermal-Stable Carbonic Anhydrases: A Structural Overview
inferred← citeshttps://doi.org/10.1007/978-94-007-7359-2_3openalex-snapshot
Catalytic Mechanism of α-Class Carbonic Anhydrases: CO2 Hydration and Proton Transfer
inferred← citeshttps://doi.org/10.1007/978-981-19-6379-7_16openalex-snapshot
Nature-Based Computing Bioinformatics Approaches in Drug Discovery Against Promising Molecular Targets Carbonic Anhydrases and Serine/Threonine Kinases for Cancer Treatment
inferred← citeshttps://doi.org/10.1007/978-981-99-7808-3_16openalex-snapshot
Naturbasierte bioinformatische Ansätze in der Arzneimittelforschung gegen vielversprechende molekulare Ziele – Carbonanhydrasen und Serin/Threonin-Kinasen zur Krebsbehandlung
inferred← citeshttps://doi.org/10.1007/s00018-018-2798-8openalex-snapshot
Biochemical, biophysical and molecular dynamics studies on the proteoglycan-like domain of carbonic anhydrase IX
inferred← citeshttps://doi.org/10.1007/s00018-020-03697-3openalex-snapshot
Intrinsically disordered features of carbonic anhydrase IX proteoglycan-like domain
inferred← citeshttps://doi.org/10.1007/s00044-019-02329-1openalex-snapshot
Activation and inhibition effects of some natural products on human cytosolic CAI and CAII
inferred← citeshttps://doi.org/10.1007/s00044-020-02661-xopenalex-snapshot
Benzilydene and thiourea derivatives as new classes of carbonic anhydrase inhibitors: an in vitro and molecular docking study
inferred← citeshttps://doi.org/10.1007/s00044-022-02943-6openalex-snapshot
Design, synthesis and molecular docking studies of novel benzimidazole-1,3,4-oxadiazole hybrids for their carbonic anhydrase inhibitory and antioxidant effects
inferred← citeshttps://doi.org/10.1007/s00044-022-02978-9openalex-snapshot
The potential of chalcone derivatives as human carbonic anhydrase inhibitors in the therapy of glaucoma
inferred← citeshttps://doi.org/10.1007/s00044-023-03031-zopenalex-snapshot
Synthesis of nitrogen-containing oleanolic acid derivatives as carbonic anhydrase and acetylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.1007/s00044-026-03605-7openalex-snapshot
Dual-target carbonic anhydrase inhibitors in cancer therapy: progress, challenges, and opportunities
inferred← citeshttps://doi.org/10.1007/s00249-017-1256-0openalex-snapshot
Intrinsic thermodynamics of high affinity inhibitor binding to recombinant human carbonic anhydrase IV
inferred← citeshttps://doi.org/10.1007/s00436-018-6127-9openalex-snapshot
Plasmodium genomics: an approach for learning about and ending human malaria
inferred← citeshttps://doi.org/10.1007/s00449-016-1709-3openalex-snapshot
Expression and characterization of a codon-optimized alkaline-stable carbonic anhydrase from Aliivibrio salmonicida for CO2 sequestration applications
inferred← citeshttps://doi.org/10.1007/s00726-021-03063-yopenalex-snapshot
Post-translational modifications in tumor-associated carbonic anhydrases
inferred← citeshttps://doi.org/10.1007/s00775-020-01818-8openalex-snapshot
Native mass spectrometry of human carbonic anhydrase I and its inhibitor complexes
inferred← citeshttps://doi.org/10.1007/s00775-023-02010-4openalex-snapshot
Ferrocene-based nitroheterocyclic sulfonylhydrazones: design, synthesis, characterization and trypanocidal properties
inferred← citeshttps://doi.org/10.1007/s00894-026-06760-1openalex-snapshot
Carbonic anhydrase under the computational lens: a review of advances, challenges, and future directions
inferred← citeshttps://doi.org/10.1007/s10593-015-1748-8openalex-snapshot
In a search for selective inhibitors of carbonic anhydrases: coumarin and its bioisosteres – synthesis and derivatization
inferred← citeshttps://doi.org/10.1007/s10822-026-00832-3openalex-snapshot
Integrated computational modeling of chalcone-based inhibitors targeting carbonic anhydrase I and II: 3D-QSAR, molecular docking, and dynamics simulations
inferred← citeshttps://doi.org/10.1007/s11030-022-10527-0openalex-snapshot
Novel bis-ureido-substituted sulfaguanidines and sulfisoxazoles as carbonic anhydrase and acetylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.1007/s11030-024-11023-3openalex-snapshot
Insight on novel sulfamoylphenyl pyrazole derivatives as anticancer carbonic anhydrase inhibitors
inferred← citeshttps://doi.org/10.1007/s11030-026-11543-0openalex-snapshot
Quinazoline-sulfonamide hybrids as multitarget anticancer agents: inhibition of carbonic anhydrase IX/XII isoforms and VEGFR-2 with in vitro and in silico validation
inferred← citeshttps://doi.org/10.1007/s11033-021-06753-8openalex-snapshot
Tip60 might be a candidate for the acetylation of hepatic carbonic anhydrase I and III in mice
inferred← citeshttps://doi.org/10.1007/s11099-017-0685-4openalex-snapshot
Carbonic anhydrase - a universal enzyme of the carbon-based life
inferred← citeshttps://doi.org/10.1007/s11164-017-2903-xopenalex-snapshot
Anticancer and radio-sensitizing evaluation of some new sulfonamide derivatives bearing pyridone, thiophene, and hydrazone moieties
inferred← citeshttps://doi.org/10.1007/s11172-019-2449-8openalex-snapshot
Acidity of arylsulfonamides as function of quantum chemical parameters of sulfonamide nitrogen
inferred← citeshttps://doi.org/10.1007/s11696-026-04771-zopenalex-snapshot
Synthesis, enzyme inhibition, in silico molecular docking and DFT analysis of novel multi-functionalized thiourea and thiazolidinone benzenesulfonamides
inferred← citeshttps://doi.org/10.1007/s13318-024-00903-6openalex-snapshot
Inhibitory Effect of Two Carbonic Anhydrases Inhibitors on the Activity of Major Cytochrome P450 Enzymes
inferred← citeshttps://doi.org/10.1007/s13369-025-10852-0openalex-snapshot
A Review on CO2 Mitigation by Modified Microbial Carbonic Anhydrase Enzyme (CA)
inferred← citeshttps://doi.org/10.1007/s13738-026-03424-yopenalex-snapshot
In vitro and in silico evaluation of a new schiff base: carbonic anhydrase I and II enzyme inhibition, molecular docking, and dynamic behaviour
inferred← citeshttps://doi.org/10.1007/s40820-021-00616-4openalex-snapshot
Targeting Hypoxic Tumors with Hybrid Nanobullets for Oxygen-Independent Synergistic Photothermal and Thermodynamic Therapy
inferred← citeshttps://doi.org/10.1007/s43440-020-00149-4openalex-snapshot
Evaluation of some thiophene-based sulfonamides as potent inhibitors of carbonic anhydrase I and II isoenzymes isolated from human erythrocytes by kinetic and molecular modelling studies
inferred← citeshttps://doi.org/10.1007/s43538-026-00880-1openalex-snapshot
Computational investigation of novel acetazolamide derivatives as human carbonic anhydrase XII inhibitors: electronic structure, binding interactions, molecular dynamics and pharmacokinetic evaluation
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14880-2openalex-snapshot
1,3,4-Thiadiazoles
inferred← citeshttps://doi.org/10.1016/b978-0-12-800167-7.00017-1openalex-snapshot
Tumor Microenvironment as Target in Cancer Therapy
inferred← citeshttps://doi.org/10.1016/b978-0-12-803740-9.00013-5openalex-snapshot
Synthesis of Fluorinated Nitrogen-Containing Compounds Through Superelectrophilic Activation in Superacid HF/SbF5∗∗This work is dedicated to Pr Jean-Claude Jacquesy with great consideration.
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00001-0openalex-snapshot
Carbonic anhydrases
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00002-2openalex-snapshot
α-Carbonic anhydrases
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00006-xopenalex-snapshot
ζ-Carbonic anhydrases
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00007-1openalex-snapshot
η- and θ-carbonic anhydrases
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00008-3openalex-snapshot
Human carbonic anhydrases
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00009-5openalex-snapshot
Mechanisms of action of carbonic anhydrase inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00010-1openalex-snapshot
Mechanisms of action of carbonic anhydrase inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00011-3openalex-snapshot
Mechanism of action of carbonic anhydrase inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00014-9openalex-snapshot
Carbonic anhydrase inhibitors as diuretics
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00015-0openalex-snapshot
Carbonic anhydrase inhibitors for the treatment of epilepsy and obesity
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00016-2openalex-snapshot
Carbonic anhydrase inhibitors for the treatment of tumors
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00017-4openalex-snapshot
Carbonic anhydrase inhibitors for the treatment of neuropathic pain and arthritis
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00019-8openalex-snapshot
Carbonic anhydrases from pathogens
inferred← citeshttps://doi.org/10.1016/b978-0-12-816476-1.00021-6openalex-snapshot
Carbonic anhydrase activators and their potential in the pharmaceutical field
inferred← citeshttps://doi.org/10.1016/b978-0-12-816545-4.00012-8openalex-snapshot
Carbonic Anhydrase Inhibitor—NO Donor Hybrids and Their Pharmacological Applications
inferred← citeshttps://doi.org/10.1016/b978-0-12-820701-7.00013-0openalex-snapshot
Molecular docking studies and virtual drug screening of chemosensitizers
inferred← citeshttps://doi.org/10.1016/b978-0-12-820701-7.00014-2openalex-snapshot
Design, synthesis, and biological evaluation of selective hCA IX inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-12-820701-7.00015-4openalex-snapshot
Small molecules and monoclonal antibodies as selective hCA XII inhibitors: An update
inferred← citeshttps://doi.org/10.1016/b978-0-12-823144-9.00161-8openalex-snapshot
Metal ion homeostasis: Metalloenzyme paralogs in the bacterial adaptative response to zinc restriction
inferred← citeshttps://doi.org/10.1016/b978-0-12-823974-2.00025-5openalex-snapshot
CDCA1, a versatile member of the ζ-class of carbonic anhydrase family
inferred← citeshttps://doi.org/10.1016/b978-0-443-22204-7.00014-9openalex-snapshot
Molecular targets for Trichomonas vaginalis
inferred← citeshttps://doi.org/10.1016/b978-0-444-63258-6.00001-9openalex-snapshot
Carbonic Anhydrases: An Overview
inferred← citeshttps://doi.org/10.1016/b978-0-444-63258-6.00002-0openalex-snapshot
Human Carbonic Anhydrases: Catalytic Properties, Structural Features, and Tissue Distribution
inferred← citeshttps://doi.org/10.1016/b978-0-444-63258-6.00003-2openalex-snapshot
Carbonic Anhydrase I
inferred← citeshttps://doi.org/10.1016/b978-0-444-63258-6.00004-4openalex-snapshot
Carbonic Anhydrase II as Target for Drug Design
inferred← citeshttps://doi.org/10.1016/b978-0-444-63258-6.00009-3openalex-snapshot
Carbonic Anhydrase VII
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