| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/J.BMC.2007.04.020 |
| P698 | PubMed publication ID | 17475500 |
| P50 | author | Andrea Scozzafava | Q28037168 |
| Claudiu T Supuran | Q28211545 | ||
| P433 | issue | 13 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | ethoxzolamide | Q265352 |
| P304 | page(s) | 4336-4350 | |
| P577 | publication date | 2007-04-19 | |
| P1433 | published in | Bioorganic & Medicinal Chemistry | Q2904200 |
| P1476 | title | Carbonic anhydrases as targets for medicinal chemistry | |
| P478 | volume | 15 |
| Q85085186 | A multivariate approach for the determination of isoelectric point of human carbonic anhydrase isoforms by capillary isoelectric focusing |
| Q28395209 | A new role for carbonic anhydrase 2 in the response of fish to copper and osmotic stress: implications for multi-stressor studies |
| Q27650004 | A novel acetate-bound complex of human carbonic anhydrase II |
| Q51638578 | Acetylcholinesterase and carbonic anhydrase isoenzymes I and II inhibition profiles of taxifolin. |
| Q95851946 | Activation of Two Different Drugs Used in Alzheimer's Disease Treatment on Human Carbonic Anhydrase Isozymes I and II Activity: an In Vitro Study |
| Q41240143 | Anomeric Effects in Sulfamides. |
| Q53080841 | Antipsychotic agents screened as human carbonic anhydrase I and II inhibitors. |
| Q47860232 | Biochemical characterization of the γ-carbonic anhydrase from the oral pathogen Porphyromonas gingivalis, PgiCA. |
| Q38031636 | Bismuth compounds in medicinal chemistry. |
| Q39192041 | Calmodulin as a potential target by which berberine induces cell cycle arrest in human hepatoma Bel7402 cells |
| Q87385831 | Capsaicin: a potent inhibitor of carbonic anhydrase isoenzymes |
| Q64277291 | Carbonic Anhydrase Inhibitors of Different Structures Dilate Pre-Contracted Porcine Retinal Arteries |
| Q36424700 | Carbonic anhydrase I as a new plasma biomarker for prostate cancer. |
| Q38026869 | Carbonic anhydrase III: a neglected isozyme is stepping into the limelight |
| Q38064308 | Carbonic anhydrase as pollution biomarker: an ancient enzyme with a new use |
| Q39962844 | Carbonic anhydrase in the scleractinian coral Stylophora pistillata: characterization, localization, and role in biomineralization |
| Q38796112 | Carbonic anhydrase inhibition and cytotoxicity studies of Mannich base derivatives of thymol. |
| Q37783942 | Carbonic anhydrase inhibition with natural products: novel chemotypes and inhibition mechanisms |
| Q37909406 | Carbonic anhydrase inhibitors and activators for novel therapeutic applications |
| Q58863232 | Carbonic anhydrase inhibitors. Cloning, characterization and inhibition studies of the cytosolic isozyme III with anions |
| Q46290410 | Carbonic anhydrase inhibitors: design of membrane-impermeant copper(II) complexes of DTPA-, DOTA-, and TETA-tailed sulfonamides targeting the tumor-associated transmembrane isoform IX. |
| Q58863142 | Carbonic anhydrase inhibitors: guaiacol and catechol derivatives effectively inhibit certain human carbonic anhydrase isoenzymes (hCA I, II, IX and XII) |
| Q46014247 | Carbonic anhydrase inhibitors: in vitro inhibition of α isoforms (hCA I, hCA II, bCA III, hCA IV) by flavonoids. |
| Q38223680 | Carbonic anhydrases and their biotechnological applications |
| Q33838825 | Characterization and inhibition studies of an α-carbonic anhydrase from the endangered sturgeon species Acipenser gueldenstaedti. |
| Q46682128 | Characterization and inhibition studies of carbonic anhydrase from gill of Russian Sturgeon Fish (Acipenser gueldenstaedtii). |
| Q27662971 | Coumarinyl-substituted sulfonamides strongly inhibit several human carbonic anhydrase isoforms: solution and crystallographic investigations |
| Q30804652 | Coupling Protein Dynamics with Proton Transport in Human Carbonic Anhydrase II. |
| Q88754770 | Cryptophane Nanoscale Assemblies Expand 129Xe NMR Biosensing |
| Q41963820 | Cryptophane xenon-129 nuclear magnetic resonance biosensors targeting human carbonic anhydrase |
| Q46616542 | Discovering isozyme-selective inhibitor scaffolds of human carbonic anhydrases using structural alignment and de novo drug design approaches |
| Q50206375 | Discovery of potent carbonic anhydrase, acetylcholinesterase, and butyrylcholinesterase enzymes inhibitors: The new amides and thiazolidine-4-ones synthesized on an acetophenone base |
| Q39606437 | Docking, synthesis, and in vitro evaluation of antimitotic estrone analogs |
| Q42592226 | Downregulation of carbonic anhydrase IX promotes Col10a1 expression in chondrocytes |
| Q38690809 | Emerging Roles of Carbonyl Sulfide in Chemical Biology: Sulfide Transporter or Gasotransmitter? |
| Q58692250 | Enzymatic Carbon Dioxide Capture |
| Q36581797 | Evaluation of CAIX and CAXII Expression in Breast Cancer at Varied O2 Levels: CAIX is the Superior Surrogate Imaging Biomarker of Tumor Hypoxia |
| Q48279352 | Evaluation of acetylcholinesterase and carbonic anhydrase inhibition profiles of 1,2,3,4,6-pentasubstituted-4-hydroxy-cyclohexanes. |
| Q37096976 | Ex vivo apoptotic and autophagic influence of an estradiol analogue on platelets. |
| Q38102745 | Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors |
| Q55052402 | Expression of Carbonic Anhydrase III, a Nucleus Pulposus Phenotypic Marker, is Hypoxia-responsive and Confers Protection from Oxidative Stress-induced Cell Death. |
| Q39596916 | Generation and characterization of the first inhibitory antibody targeting tumour-associated carbonic anhydrase XII. |
| Q36644164 | Global Mapping of Traditional Chinese Medicine into Bioactivity Space and Pathways Annotation Improves Mechanistic Understanding and Discovers Relationships between Therapeutic Action (Sub)classes |
| Q39663504 | Guanylate cyclase-G, expressed in the Grueneberg ganglion olfactory subsystem, is activated by bicarbonate |
| Q38653464 | How many carbonic anhydrase inhibition mechanisms exist? |
| Q42025945 | Hydrophobic substituents of the phenylmethylsulfamide moiety can be used for the development of new selective carbonic anhydrase inhibitors |
| Q40816292 | Identification of Interaction Hot Spots in Structures of Drug Targets on the Basis of Three-Dimensional Activity Cliff Information |
| Q30045768 | In vitro cytotoxic evaluation of some new heterocyclic sulfonamide derivatives |
| Q46449939 | In vitro effects of an in silico-modelled 17β-estradiol derivative in combination with dichloroacetic acid on MCF-7 and MCF-12A cells. |
| Q28484595 | In vitro evaluation of ESE-15-ol, an estradiol analogue with nanomolar antimitotic and carbonic anhydrase inhibitory activity |
| Q36945018 | Increased propensity for calcium phosphate kidney stones with topiramate use. |
| Q64888569 | Indole-Based Hydrazones Containing A Sulfonamide Moiety as Selective Inhibitors of Tumor-Associated Human Carbonic Anhydrase Isoforms IX and XII. |
| Q27659917 | Inhibition and binding studies of carbonic anhydrase isozymes I, II and IX with benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulphonamides |
| Q41974565 | Inhibition of carbonic anhydrase IX as a novel anticancer mechanism |
| Q38742510 | Inhibition of carbonic anhydrase from Trypanosoma cruzi for the management of Chagas disease: an underexplored therapeutic opportunity |
| Q45895475 | Inhibition of carbonic anhydrase isozymes I and II with natural products extracted from plants, mushrooms and honey. |
| Q42476931 | Intrinsic thermodynamics of ethoxzolamide inhibitor binding to human carbonic anhydrase XIII. |
| Q51563840 | 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. |
| Q34660349 | Malaria parasite carbonic anhydrase: inhibition of aromatic/heterocyclic sulfonamides and its therapeutic potential |
| Q47696436 | Mechanisms of acid-base regulation in peritoneal dialysis |
| Q38048811 | Medicinal significance of benzothiazole scaffold: an insight view |
| Q61795859 | Modes of Accessing Bicarbonate for the Regulation of Membrane Guanylate Cyclase (ROS-GC) in Retinal Rods and Cones |
| Q47069474 | Molecular and biochemical analysis of the beta class carbonic anhydrases in Caenorhabditis elegans |
| Q54297430 | Monoclonal antibodies raised against 167-180 aa sequence of human carbonic anhydrase XII inhibit its enzymatic activity. |
| Q48365232 | Natural product inhibitors of carbonic anhydrase I and II isoenzymes: osajin and pomiferin. |
| Q34035225 | Noninvasive detection of breast cancer lymph node metastasis using carbonic anhydrases IX and XII targeted imaging probes |
| Q61798855 | Novel 2-indolinones containing a sulfonamide moiety as selective inhibitors of candida β-carbonic anhydrase enzyme |
| Q90180795 | Novel 2-substituted-benzimidazole-6-sulfonamides as carbonic anhydrase inhibitors: synthesis, biological evaluation against isoforms I, II, IX and XII and molecular docking studies |
| Q36769323 | Novel chloroquinoline derivatives incorporating biologically active benzenesulfonamide moiety: synthesis, cytotoxic activity and molecular docking |
| Q35100992 | Novel estradiol analogue induces apoptosis and autophagy in esophageal carcinoma cells. |
| Q44649427 | Novel organometallic cationic ruthenium(II) pentamethylcyclopentadienyl benzenesulfonamide complexes targeted to inhibit carbonic anhydrase |
| Q27677127 | Potent inhibition of dinuclear zinc(II) peptidase, an aminopeptidase from Aeromonas proteolytica, by 8-quinolinol derivatives: inhibitor design based on Zn2+ fluorophores, kinetic, and X-ray crystallographic study |
| Q33523595 | Profiling the NIH Small Molecule Repository for compounds that generate H2O2 by redox cycling in reducing environments |
| Q54285789 | Protonography, a new technique for the analysis of carbonic anhydrase activity. |
| Q35592559 | Quantitative proteomic analysis revealed lovastatin-induced perturbation of cellular pathways in HL-60 cells |
| Q40728538 | Reduction in mdx mouse muscle degeneration by low-intensity endurance exercise: a proteomic analysis in quadriceps muscle of exercised compared with sedentary mdx mice |
| Q42555938 | Regulating enzymatic activity with a photoswitchable affinity label |
| Q28829960 | Self-Immolative Thiocarbamates Provide Access to Triggered H2S Donors and Analyte Replacement Fluorescent Probes |
| Q28485895 | Signaling pathways of ESE-16, an antimitotic and anticarbonic anhydrase estradiol analog, in breast cancer cells |
| Q37145164 | Significance of pH regulation and carbonic anhydrases in tumour progression and implications for diagnostic and therapeutic approaches. |
| Q34041312 | Significant proteins affecting cerebral vasospasm using complementary ICPMS and MALDI-MS. |
| Q43187836 | Some QSAR studies for a group of sulfonamide Schiff base as carbonic anhydrase CA II inhibitors |
| Q45804276 | Structural modulation of the biological activity of gold nanoparticles functionalized with a carbonic anhydrase inhibitor. |
| Q27650547 | Structure of a 129 Xe-Cryptophane Biosensor Complexed with Human Carbonic Anhydrase II |
| Q40651976 | Structure of α-carbonic anhydrase from the human pathogen Helicobacter pylori |
| Q37999063 | Structure-based drug discovery of carbonic anhydrase inhibitors |
| Q42061370 | Sulfa drugs as inhibitors of carbonic anhydrase: new targets for the old drugs |
| Q48309908 | Synthesis and Carbonic Anhydrase Inhibition of Tetrabromo Chalcone Derivatives. |
| Q59011135 | Synthesis and Evaluation of New Phthalazine Urea and Thiourea Derivatives as Carbonic Anhydrase Inhibitors |
| Q48351281 | Synthesis and bioactivity of several new hetaryl sulfonamides. |
| Q48000247 | Synthesis and biological evaluation of histamine Schiff bases as carbonic anhydrase I, II, IV, VII, and IX activators. |
| Q45361683 | Synthesis and biological evaluation of novel bromophenol derivatives as carbonic anhydrase inhibitors |
| Q48261474 | Synthesis and biological evaluation of phloroglucinol derivatives possessing α-glycosidase, acetylcholinesterase, butyrylcholinesterase, carbonic anhydrase inhibitory activity |
| Q44510176 | Synthesis and carbonic anhydrase inhibitory properties of 1,3-dicarbonyl derivatives of methylaminobenzene-sulfonamide. |
| Q44015636 | Synthesis and carbonic anhydrase isoenzymes I and II inhibitory effects of novel benzylamine derivatives |
| Q85066457 | Synthesis and characterisation of two novel proton transfer compounds and their inhibition studies on carbonic anhydrase isoenzymes |
| Q44503516 | Synthesis and characterization of a proton transfer salt between 2,6-pyridinedicarboxylic acid and 2-aminobenzothiazole, and its complexes and their inhibition studies on carbonic anhydrase isoenzymes |
| Q92500292 | Synthesis and human carbonic anhydrase I, II, VA, and XII inhibition with novel amino acid-sulphonamide conjugates |
| Q35828840 | Synthesis and molecular structure of novel 2-(alkylthio)-4-chloro-N-(4,5-dihydro-5-oxo-1H-1,2,4-triazol-3-yl)-5-methylbenzenesulfonamides with potential anticancer activity |
| Q60931418 | Synthesis carbonic anhydrase enzyme inhibition and antioxidant activity of novel benzothiazole derivatives incorporating glycine, methionine, alanine, and phenylalanine moieties |
| Q31030668 | Synthesis of 4-[2-(3,4-dimethoxybenzyl)cyclopentyl]-1,2-dimethoxybenzene Derivatives and Evaluations of Their Carbonic Anhydrase Isoenzymes Inhibitory Effects |
| Q48316404 | Synthesis of some novel pyridine compounds containing bis-1,2,4-triazole/thiosemicarbazide moiety and investigation of their antioxidant properties, carbonic anhydrase, and acetylcholinesterase enzymes inhibition profiles. |
| Q50245617 | Synthesis of some tetrahydropyrimidine-5-carboxylates, determination of their metal chelating effects and inhibition profiles against acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase |
| Q38748892 | Synthesis, cytotoxicity and carbonic anhydrase inhibitory activities of new pyrazolines |
| Q48293922 | Synthesis, molecular modeling, and biological evaluation of 4-[5-aryl-3-(thiophen-2-yl)-4,5-dihydro-1H-pyrazol-1-yl] benzenesulfonamides toward acetylcholinesterase, carbonic anhydrase I and II enzymes. |
| Q26770101 | The Complex Relationship between Metals and Carbonic Anhydrase: New Insights and Perspectives |
| Q90544035 | The Human Carbonic Anhydrase II in Platelets: An Underestimated Field of Its Activity |
| Q92189868 | The carbonic anhydrase of Clostridium autoethanogenum represents a new subclass of β-carbonic anhydrases |
| Q50463216 | The effects of anti-epileptic drugs on human erythrocyte carbonic anhydrase I and II isozymes. |
| Q41231506 | The effects of bronchodilator drugs and antibiotics used for respiratory infection on human erythrocyte carbonic anhydrase I and II isozymes |
| Q38537265 | The history and rationale of using carbonic anhydrase inhibitors in the treatment of peptic ulcers. In memoriam Ioan Puşcaş (1932-2015). |
| Q35312408 | The screening of RNA aptamers specific for carbonic anhydrase I using the Systematic Evolution of Ligands by an Exponential Enrichment Method (SELEX). |
| Q27688043 | The structural comparison between membrane-associated human carbonic anhydrases provides insights into drug design of selective inhibitors |
| Q28492566 | Three functional β-carbonic anhydrases in Pseudomonas aeruginosa PAO1: role in survival in ambient air |
| Q35145047 | Transport activity of the high-affinity monocarboxylate transporter MCT2 is enhanced by extracellular carbonic anhydrase IV but not by intracellular carbonic anhydrase II |
| Q90727312 | Use of an immobilised thermostable α-CA (SspCA) for enhancing the metabolic efficiency of the freshwater green microalga Chlorella sorokiniana |
| Q33951488 | Zn(II)-coordination modulated ligand photophysical processes - the development of fluorescent indicators for imaging biological Zn(II) ions |
| Q57816680 | α-Carbonic anhydrases are sulfatases with cyclic diol monosulfate esters |
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