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For: Supuran CT, Capasso C. Biomedical applications of prokaryotic carbonic anhydrases. Expert Opin Ther Pat 2018;28:745-54. [PMID: 29973089 DOI: 10.1080/13543776.2018.1497161] [Cited by in Crossref: 38] [Cited by in F6Publishing: 46] [Article Influence: 9.5] [Reference Citation Analysis]
Number Citing Articles
1 Del Prete S, Bua S, Alasmary FAS, AlOthman Z, Tambutté S, Zoccola D, Supuran CT, Capasso C. Comparison of the Sulfonamide Inhibition Profiles of the α-Carbonic Anhydrase Isoforms (SpiCA1, SpiCA2 and SpiCA3) Encoded by the Genome of the Scleractinian Coral Stylophora pistillata. Mar Drugs 2019;17:E146. [PMID: 30832211 DOI: 10.3390/md17030146] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
2 Pustenko A, Nocentini A, Balašova A, Krasavin M, Žalubovskis R, Supuran CT. 7-Acylamino-3H-1,2-benzoxathiepine 2,2-dioxides as new isoform-selective carbonic anhydrase IX and XII inhibitors. J Enzyme Inhib Med Chem 2020;35:650-6. [PMID: 32079427 DOI: 10.1080/14756366.2020.1722658] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Akgul O, Angeli A, Selleri S, Capasso C, Supuran CT, Carta F. Taurultams incorporating arylsulfonamide: First in vitro inhibition studies of α-, β- and γ-class Carbonic Anhydrases from Vibrio cholerae and Burkholderia pseudomallei. Eur J Med Chem 2021;219:113444. [PMID: 33866238 DOI: 10.1016/j.ejmech.2021.113444] [Reference Citation Analysis]
4 Supuran CT, Capasso C. A Highlight on the Inhibition of Fungal Carbonic Anhydrases as Drug Targets for the Antifungal Armamentarium. Int J Mol Sci 2021;22:4324. [PMID: 33919261 DOI: 10.3390/ijms22094324] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Llanos MA, Sbaraglini ML, Villalba ML, Ruiz MD, Carrillo C, Alba Soto C, Talevi A, Angeli A, Parkkila S, Supuran CT, Gavernet L. A structure-based approach towards the identification of novel antichagasic compounds: Trypanosoma cruzi carbonic anhydrase inhibitors. J Enzyme Inhib Med Chem 2020;35:21-30. [PMID: 31619095 DOI: 10.1080/14756366.2019.1677638] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
6 Urbański LJ, Angeli A, Hytönen VP, Di Fiore A, Parkkila S, De Simone G, Supuran CT. Inhibition of the newly discovered β‑carbonic anhydrase from the protozoan pathogen Trichomonas vaginalis with inorganic anions and small molecules. J Inorg Biochem 2020;213:111274. [PMID: 33068968 DOI: 10.1016/j.jinorgbio.2020.111274] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
7 Bua S, Osman SM, Del Prete S, Capasso C, Alothman Z, Nocentini A, Supuran CT. Click-tailed benzenesulfonamides as potent bacterial carbonic anhydrase inhibitors for targeting Mycobacterium tuberculosis and Vibrio cholerae. Bioorganic Chemistry 2019;86:183-6. [DOI: 10.1016/j.bioorg.2019.01.065] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 3.3] [Reference Citation Analysis]
8 Del Prete S, Bua S, Supuran CT, Capasso C. Escherichia coli γ-carbonic anhydrase: characterisation and effects of simple aromatic/heterocyclic sulphonamide inhibitors. J Enzyme Inhib Med Chem 2020;35:1545-54. [PMID: 32746656 DOI: 10.1080/14756366.2020.1800670] [Cited by in Crossref: 4] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
9 Supuran CT. Exploring the multiple binding modes of inhibitors to carbonic anhydrases for novel drug discovery. Expert Opin Drug Discov 2020;15:671-86. [PMID: 32208982 DOI: 10.1080/17460441.2020.1743676] [Cited by in Crossref: 25] [Cited by in F6Publishing: 41] [Article Influence: 12.5] [Reference Citation Analysis]
10 Grandāne A, Nocentini A, Domračeva I, Žalubovskis R, Supuran CT. Development of oxathiino[6,5-b]pyridine 2,2-dioxide derivatives as selective inhibitors of tumor-related carbonic anhydrases IX and XII. Eur J Med Chem 2020;200:112300. [PMID: 32460112 DOI: 10.1016/j.ejmech.2020.112300] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
11 Nocentini A, Hewitt CS, Mastrolorenzo MD, Flaherty DP, Supuran CT. Anion inhibition studies of the α-carbonic anhydrases from Neisseria gonorrhoeae. J Enzyme Inhib Med Chem 2021;36:1061-6. [PMID: 34030562 DOI: 10.1080/14756366.2021.1929202] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Angeli A, Ferraroni M, Pinteala M, Maier SS, Simionescu BC, Carta F, Del Prete S, Capasso C, Supuran CT. Crystal Structure of a Tetrameric Type II β-Carbonic Anhydrase from the Pathogenic Bacterium Burkholderia pseudomallei. Molecules 2020;25:E2269. [PMID: 32408533 DOI: 10.3390/molecules25102269] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
13 Supuran CT. Coumarin carbonic anhydrase inhibitors from natural sources. J Enzyme Inhib Med Chem 2020;35:1462-70. [PMID: 32779543 DOI: 10.1080/14756366.2020.1788009] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]
14 Supuran CT. Experimental Carbonic Anhydrase Inhibitors for the Treatment of Hypoxic Tumors. J Exp Pharmacol 2020;12:603-17. [PMID: 33364855 DOI: 10.2147/JEP.S265620] [Cited by in Crossref: 19] [Cited by in F6Publishing: 12] [Article Influence: 9.5] [Reference Citation Analysis]
15 Del Prete S, Merlo R, Valenti A, Mattossovich R, Rossi M, Carginale V, Supuran CT, Perugino G, Capasso C. Thermostability enhancement of the α-carbonic anhydrase from Sulfurihydrogenibium yellowstonense by using the anchoring-and-self-labelling-protein-tag system (ASLtag). J Enzyme Inhib Med Chem 2019;34:946-54. [PMID: 31039618 DOI: 10.1080/14756366.2019.1605991] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
16 Vullo D, Lehneck R, Donald WA, Pöggeler S, Supuran CT. Sulfonamide Inhibition Studies of the β-Class Carbonic Anhydrase CAS3 from the Filamentous Ascomycete Sordaria macrospora. Molecules 2020;25:E1036. [PMID: 32106611 DOI: 10.3390/molecules25051036] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
17 Bua S, Haapanen S, Kuuslahti M, Parkkila S, Supuran CT. Sulfonamide Inhibition Studies of a New β-Carbonic Anhydrase from the Pathogenic Protozoan Entamoeba histolytica. Int J Mol Sci 2018;19:E3946. [PMID: 30544802 DOI: 10.3390/ijms19123946] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
18 Vullo D, Lehneck R, Donald WA, Pöggeler S, Supuran CT. Anion Inhibition Studies of the β-Class Carbonic Anhydrase CAS3 from the Filamentous Ascomycete Sordaria macrospora. Metabolites 2020;10:E93. [PMID: 32151102 DOI: 10.3390/metabo10030093] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
19 Alissa SA, Alghulikah HA, Alothman ZA, Osman SM, Del Prete S, Capasso C, Nocentini A, Supuran CT. Phosphonamidates are the first phosphorus-based zinc binding motif to show inhibition of β-class carbonic anhydrases from bacteria, fungi, and protozoa. J Enzyme Inhib Med Chem 2020;35:59-64. [PMID: 31663383 DOI: 10.1080/14756366.2019.1681987] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
20 Al-Sanea MM, Elkamhawy A, Paik S, Bua S, Ha Lee S, Abdelgawad MA, Roh EJ, Eldehna WM, Supuran CT. Synthesis and biological evaluation of novel 3-(quinolin-4-ylamino)benzenesulfonamidesAQ3 as carbonic anhydrase isoforms I and II inhibitors. J Enzyme Inhib Med Chem 2019;34:1457-64. [PMID: 31411080 DOI: 10.1080/14756366.2019.1652282] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 3.7] [Reference Citation Analysis]
21 Del Prete S, De Luca V, Bua S, Nocentini A, Carginale V, Supuran CT, Capasso C. The Effect of Substituted Benzene-Sulfonamides and Clinically Licensed Drugs on the Catalytic Activity of CynT2, a Carbonic Anhydrase Crucial for Escherichia coli Life Cycle. Int J Mol Sci 2020;21:E4175. [PMID: 32545297 DOI: 10.3390/ijms21114175] [Cited by in Crossref: 1] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
22 Giovannuzzi S, Hewitt CS, Nocentini A, Capasso C, Flaherty DP, Supuran CT. Coumarins effectively inhibit bacterial α-carbonic anhydrases. J Enzyme Inhib Med Chem 2022;37:333-8. [PMID: 34979838 DOI: 10.1080/14756366.2021.2012174] [Reference Citation Analysis]
23 Akdemir A, Angeli A, Göktaş F, Eraslan Elma P, Karalı N, Supuran CT. Novel 2-indolinones containing a sulfonamide moiety as selective inhibitors of candida β-carbonic anhydrase enzyme. J Enzyme Inhib Med Chem 2019;34:528-31. [PMID: 30724625 DOI: 10.1080/14756366.2018.1564045] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
24 De Luca V, Petreni A, Carginale V, Scaloni A, Supuran CT, Capasso C. Effect of amino acids and amines on the activity of the recombinant ι-carbonic anhydrase from the Gram-negative bacterium Burkholderia territorii. J Enzyme Inhib Med Chem 2021;36:1000-6. [PMID: 33980103 DOI: 10.1080/14756366.2021.1919891] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
25 Provensi G, Nocentini A, Passani MB, Blandina P, Supuran CT. Activation of carbonic anhydrase isoforms involved in modulation of emotional memory and cognitive disorders with histamine agonists, antagonists and derivatives. J Enzyme Inhib Med Chem 2021;36:719-26. [PMID: 33648390 DOI: 10.1080/14756366.2021.1891051] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
26 Küçükbay H, Gönül Z, Küçükbay FZ, Angeli A, Bartolucci G, Supuran CT. Preparation, carbonic anhydrase enzyme inhibition and antioxidant activity of novel 7-amino-3,4-dihydroquinolin-2(1H)-one derivatives incorporating mono or dipeptide moiety. J Enzyme Inhib Med Chem 2020;35:1021-6. [PMID: 32297533 DOI: 10.1080/14756366.2020.1751620] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
27 Rotondi G, Guglielmi P, Carradori S, Secci D, De Monte C, De Filippis B, Maccallini C, Amoroso R, Cirilli R, Akdemir A, Angeli A, Supuran CT. Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold. J Enzyme Inhib Med Chem 2019;34:1400-13. [PMID: 31401897 DOI: 10.1080/14756366.2019.1651315] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
28 Huentupil Y, Peña L, Novoa N, Berrino E, Arancibia R, Supuran CT. New sulfonamides containing organometallic-acylhydrazones: synthesis, characterisation and biological evaluation as inhibitors of human carbonic anhydrases. J Enzyme Inhib Med Chem 2019;34:451-8. [PMID: 30734605 DOI: 10.1080/14756366.2018.1555156] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
29 Renn D, Shepard L, Vancea A, Karan R, Arold ST, Rueping M. Novel Enzymes From the Red Sea Brine Pools: Current State and Potential. Front Microbiol 2021;12:732856. [PMID: 34777282 DOI: 10.3389/fmicb.2021.732856] [Reference Citation Analysis]
30 Nocentini A, Supuran CT, Capasso C. An overview on the recently discovered iota-carbonic anhydrases. J Enzyme Inhib Med Chem 2021;36:1988-95. [PMID: 34482770 DOI: 10.1080/14756366.2021.1972995] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
31 Berrino E, Supuran CT. Novel approaches for designing drugs that interfere with pH regulation. Expert Opin Drug Discov 2019;14:231-48. [PMID: 30681011 DOI: 10.1080/17460441.2019.1567488] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 6.0] [Reference Citation Analysis]
32 Nocentini A, Osman SM, Del Prete S, Capasso C, Alothman ZA, Supuran CT. Extending the γ-class carbonic anhydrases inhibition profiles with phenolic compounds. Bioorganic Chemistry 2019;93:103336. [DOI: 10.1016/j.bioorg.2019.103336] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
33 De Luca V, Petreni A, Nocentini A, Scaloni A, Supuran CT, Capasso C. Effect of Sulfonamides and Their Structurally Related Derivatives on the Activity of ι-Carbonic Anhydrase from Burkholderia territorii. Int J Mol Sci 2021;22:E571. [PMID: 33430028 DOI: 10.3390/ijms22020571] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
34 Bonardi A, Nocentini A, Bua S, Combs J, Lomelino C, Andring J, Lucarini L, Sgambellone S, Masini E, McKenna R, Gratteri P, Supuran CT. Sulfonamide Inhibitors of Human Carbonic Anhydrases Designed through a Three-Tails Approach: Improving Ligand/Isoform Matching and Selectivity of Action. J Med Chem 2020;63:7422-44. [PMID: 32519851 DOI: 10.1021/acs.jmedchem.0c00733] [Cited by in Crossref: 11] [Cited by in F6Publishing: 17] [Article Influence: 5.5] [Reference Citation Analysis]
35 Miyazaki T, Moon JY, Shin R. Contribution of marine macroalgae genes to plant potassium deficiency tolerance in transgenic Arabidopsis. Plant Biotechnol Rep 2021;15:349-57. [DOI: 10.1007/s11816-021-00680-7] [Reference Citation Analysis]
36 Supuran CT. Carbonic anhydrase inhibitors and their potential in a range of therapeutic areas. Expert Opin Ther Pat 2018;28:709-12. [PMID: 30217119 DOI: 10.1080/13543776.2018.1523897] [Cited by in Crossref: 60] [Cited by in F6Publishing: 73] [Article Influence: 15.0] [Reference Citation Analysis]
37 Ronci M, Del Prete S, Puca V, Carradori S, Carginale V, Muraro R, Mincione G, Aceto A, Sisto F, Supuran CT, Grande R, Capasso C. Identification and characterization of the α-CA in the outer membrane vesicles produced by Helicobacter pylori. J Enzyme Inhib Med Chem 2019;34:189-95. [PMID: 30734607 DOI: 10.1080/14756366.2018.1539716] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 5.3] [Reference Citation Analysis]
38 Supuran CT. Emerging role of carbonic anhydrase inhibitors. Clin Sci (Lond) 2021;135:1233-49. [PMID: 34013961 DOI: 10.1042/CS20210040] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 8.0] [Reference Citation Analysis]
39 Blandina P, Provensi G, Passsani MB, Capasso C, Supuran CT. Carbonic anhydrase modulation of emotional memory. Implications for the treatment of cognitive disorders. J Enzyme Inhib Med Chem 2020;35:1206-14. [PMID: 32401069 DOI: 10.1080/14756366.2020.1766455] [Cited by in Crossref: 9] [Cited by in F6Publishing: 16] [Article Influence: 9.0] [Reference Citation Analysis]
40 Ozensoy Guler O, Supuran CT, Capasso C. Carbonic anhydrase IX as a novel candidate in liquid biopsy. J Enzyme Inhib Med Chem 2020;35:255-60. [PMID: 31790601 DOI: 10.1080/14756366.2019.1697251] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
41 Haapanen S, Bua S, Kuuslahti M, Parkkila S, Supuran CT. Cloning, Characterization and Anion Inhibition Studies of a β-Carbonic Anhydrase from the Pathogenic Protozoan Entamoeba histolytica. Molecules 2018;23:E3112. [PMID: 30486513 DOI: 10.3390/molecules23123112] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
42 Del Prete S, Vullo D, Ghobril C, Hitce J, Clavaud C, Marat X, Capasso C, Supuran CT. Cloning, Purification, and Characterization of a β-Carbonic Anhydrase from Malassezia restricta, an Opportunistic Pathogen Involved in Dandruff and Seborrheic Dermatitis. Int J Mol Sci 2019;20:E2447. [PMID: 31108925 DOI: 10.3390/ijms20102447] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 3.7] [Reference Citation Analysis]
43 Bonardi A, Nocentini A, Osman SM, Alasmary FA, Almutairi TM, Abdullah DS, Gratteri P, Supuran CT. Inhibition of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae with aromatic sulphonamides and clinically licenced drugs - a joint docking/molecular dynamics study. J Enzyme Inhib Med Chem 2021;36:469-79. [PMID: 33472446 DOI: 10.1080/14756366.2020.1862102] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
44 Campestre C, De Luca V, Carradori S, Grande R, Carginale V, Scaloni A, Supuran CT, Capasso C. Carbonic Anhydrases: New Perspectives on Protein Functional Role and Inhibition in Helicobacter pylori. Front Microbiol 2021;12:629163. [PMID: 33815311 DOI: 10.3389/fmicb.2021.629163] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
45 Alhameed RA, Berrino E, Almarhoon Z, El-Faham A, Supuran CT. A class of carbonic anhydrase IX/XII - selective carboxylate inhibitors. J Enzyme Inhib Med Chem 2020;35:549-54. [PMID: 31967484 DOI: 10.1080/14756366.2020.1715388] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
46 Clima L, Craciun BF, Angeli A, Petreni A, Bonardi A, Nocentini A, Carta F, Gratteri P, Pinteala M, Supuran CT. Synthesis, Computational Studies and Assessment of in Vitro Activity of Squalene Derivatives as Carbonic Anhydrase Inhibitors. ChemMedChem 2020;15:2052-7. [PMID: 32744806 DOI: 10.1002/cmdc.202000500] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
47 Bua S, Haapanen S, Kuuslahti M, Parkkila S, Supuran CT. Activation Studies of the β-Carbonic Anhydrase from the Pathogenic Protozoan Entamoeba histolytica with Amino Acids and Amines. Metabolites 2019;9:E26. [PMID: 30717275 DOI: 10.3390/metabo9020026] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
48 Amedei A, Capasso C, Nannini G, Supuran CT. Microbiota, Bacterial Carbonic Anhydrases, and Modulators of Their Activity: Links to Human Diseases? Mediators Inflamm 2021;2021:6926082. [PMID: 34803517 DOI: 10.1155/2021/6926082] [Reference Citation Analysis]
49 Bonardi A, Nocentini A, Cadoni R, Del Prete S, Dumy P, Capasso C, Gratteri P, Supuran CT, Winum JY. Benzoxaboroles: New Potent Inhibitors of the Carbonic Anhydrases of the Pathogenic Bacterium Vibrio cholerae. ACS Med Chem Lett 2020;11:2277-84. [PMID: 33214840 DOI: 10.1021/acsmedchemlett.0c00403] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
50 Urbanski LJ, Vullo D, Parkkila S, Supuran CT. An anion and small molecule inhibition study of the β-carbonic anhydrase from Staphylococcus aureus. J Enzyme Inhib Med Chem 2021;36:1088-92. [PMID: 34056990 DOI: 10.1080/14756366.2021.1931863] [Reference Citation Analysis]
51 Cao Y, Liu Y, Zhang T, Lei W, Zhang B. Comparative Analysis on Single- and Multiherb Strategies in Coronary Artery Atherosclerosis Therapy. Cardiol Res Pract 2021;2021:6621925. [PMID: 34012683 DOI: 10.1155/2021/6621925] [Reference Citation Analysis]
52 Liu Q, Bai X, Pham H, Hu J, Dinu CZ. Active Nanointerfaces Based on Enzyme Carbonic Anhydrase and Metal-Organic Framework for Carbon Dioxide Reduction. Nanomaterials (Basel) 2021;11:1008. [PMID: 33920833 DOI: 10.3390/nano11041008] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
53 Angeli A, Del Prete S, Osman SM, AlOthman Z, Donald WA, Capasso C, Supuran CT. Activation Studies of the γ-Carbonic Anhydrases from the Antarctic Marine Bacteria Pseudoalteromonas haloplanktis and Colwellia psychrerythraea with Amino Acids and Amines. Mar Drugs 2019;17:E238. [PMID: 31013612 DOI: 10.3390/md17040238] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 0.7] [Reference Citation Analysis]
54 Pustenko A, Nocentini A, Gratteri P, Bonardi A, Vozny I, Žalubovskis R, Supuran CT. The antibiotic furagin and its derivatives are isoform-selective human carbonic anhydrase inhibitors. J Enzyme Inhib Med Chem 2020;35:1011-20. [PMID: 32297543 DOI: 10.1080/14756366.2020.1752201] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]