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For: 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: 63] [Article Influence: 12.5] [Reference Citation Analysis]
Number Citing Articles
1 Supuran CT. Anti-obesity carbonic anhydrase inhibitors: challenges and opportunities. J Enzyme Inhib Med Chem 2022;37:2478-88. [PMID: 36073149 DOI: 10.1080/14756366.2022.2121393] [Reference Citation Analysis]
2 Kumar A, Siwach K, Supuran CT, Sharma PK. A decade of tail-approach based design of selective as well as potent tumor associated carbonic anhydrase inhibitors. Bioorganic Chemistry 2022;126:105920. [DOI: 10.1016/j.bioorg.2022.105920] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
3 Chu N, Wang Y, Jia H, Han J, Wang X, Hou Z. Design, Synthesis and Biological Evaluation of New Carbohydrate-Based Coumarin Derivatives as Selective Carbonic Anhydrase IX Inhibitors via “Click” Reaction. Molecules 2022;27:5464. [DOI: 10.3390/molecules27175464] [Reference Citation Analysis]
4 Pontecorvi V, Mori M, Picarazzi F, Zara S, Carradori S, Cataldi A, Angeli A, Berrino E, Chimenti P, Ciogli A, Secci D, Guglielmi P, Supuran CT. Novel Insights on Human Carbonic Anhydrase Inhibitors Based on Coumalic Acid: Design, Synthesis, Molecular Modeling Investigation, and Biological Studies. IJMS 2022;23:7950. [DOI: 10.3390/ijms23147950] [Reference Citation Analysis]
5 Arrighi G, Puerta A, Petrini A, Hicke FJ, Nocentini A, Fernandes MX, Padrón JM, Supuran CT, Fernández-bolaños JG, López Ó. Squaramide-Tethered Sulfonamides and Coumarins: Synthesis, Inhibition of Tumor-Associated CAs IX and XII and Docking Simulations. IJMS 2022;23:7685. [DOI: 10.3390/ijms23147685] [Reference Citation Analysis]
6 Aspatwar A, Barker H, Aisala H, Zueva K, Kuuslahti M, Tolvanen M, Primmer CR, Lumme J, Bonardi A, Tripathi A, Parkkila S, Supuran CT. Cloning, purification, kinetic and anion inhibition studies of a recombinant β-carbonic anhydrase from the Atlantic salmon parasite platyhelminth Gyrodactylus salaris. J Enzyme Inhib Med Chem 2022;37:1577-86. [PMID: 35637617 DOI: 10.1080/14756366.2022.2080818] [Reference Citation Analysis]
7 Zhou X, Shi M, Wang X, Xu D. Exploring the Binding Mechanism of a Supramolecular Tweezer CLR01 to 14-3-3σ Protein via Well-Tempered Metadynamics. Front Chem 2022;10:921695. [DOI: 10.3389/fchem.2022.921695] [Reference Citation Analysis]
8 Kciuk M, Gielecińska A, Mujwar S, Mojzych M, Marciniak B, Drozda R, Kontek R. Targeting carbonic anhydrase IX and XII isoforms with small molecule inhibitors and monoclonal antibodies. J Enzyme Inhib Med Chem 2022;37:1278-98. [PMID: 35506234 DOI: 10.1080/14756366.2022.2052868] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
9 Nada H, Elkamhawy A, Abdellattif MH, Angeli A, Lee CH, Supuran CT, Lee K. 4-Anilinoquinazoline-based benzenesulfonamides as nanomolar inhibitors of carbonic anhydrase isoforms I, II, IX, and XII: design, synthesis, in-vitro, and in-silico biological studies. J Enzyme Inhib Med Chem 2022;37:994-1004. [PMID: 35350942 DOI: 10.1080/14756366.2022.2055553] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Banoglu E, Ercanlı T, Gür Maz T, Vullo D, Bonardi A, Gratteri P, Supuran CT. A Series of Thiadiazolyl-Benzenesulfonamides Incorporating an Aromatic Tail as Isoform-Selective, Potent Carbonic Anhydrase II/XII Inhibitors. ChemMedChem 2022;:e202200056. [PMID: 35266325 DOI: 10.1002/cmdc.202200056] [Reference Citation Analysis]
11 Khatua S, Taraphder S. In the footsteps of an inhibitor unbinding from the active site of human carbonic anhydrase II. Journal of Biomolecular Structure and Dynamics. [DOI: 10.1080/07391102.2022.2048075] [Reference Citation Analysis]
12 Kumar A, Siwach K, Rom T, Kumar R, Angeli A, Kumar Paul A, Supuran CT, Sharma PK. Tail-approach based design and synthesis of Arylthiazolylhydrazono-1,2,3-triazoles incorporating sulfanilamide and metanilamide as human carbonic anhydrase I, II, IV and IX inhibitors. Bioorganic Chemistry 2022. [DOI: 10.1016/j.bioorg.2022.105764] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Elkamhawy A, Woo J, Nada H, Angeli A, Bedair TM, Supuran CT, Lee K. Identification of Novel and Potent Indole-Based Benzenesulfonamides as Selective Human Carbonic Anhydrase II Inhibitors: Design, Synthesis, In Vitro, and In Silico Studies. Int J Mol Sci 2022;23:2540. [PMID: 35269684 DOI: 10.3390/ijms23052540] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Merabti A, Roger M, Nguyen C, Nocentini A, Gerbier P, Richeter S, Gary‐bobo M, Supuran CT, Clément S, Winum J. Carbonic Anhydrase Inhibitors Featuring a Porphyrin Scaffold: Synthesis, Optical and Biological Properties. European J Organic Chem. [DOI: 10.1002/ejoc.202101538] [Reference Citation Analysis]
15 Mori M, Supuran CT. Acipimox inhibits human carbonic anhydrases. J Enzyme Inhib Med Chem 2022;37:672-9. [PMID: 35139721 DOI: 10.1080/14756366.2022.2037579] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
16 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] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
17 Petreni A, Osman SM, Alasmary FA, Almutairi TM, Nocentini A, Supuran CT. Binding site comparison for coumarin inhibitors and amine/amino acid activators of human carbonic anhydrases. Eur J Med Chem 2021;226:113875. [PMID: 34634741 DOI: 10.1016/j.ejmech.2021.113875] [Cited by in Crossref: 1] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
18 Giovannuzzi S, Abutaleb NS, Hewitt CS, Carta F, Nocentini A, Seleem MN, Flaherty DP, Supuran CT. Dithiocarbamates effectively inhibit the α-carbonic anhydrase from Neisseria gonorrhoeae. J Enzyme Inhib Med Chem 2022;37:1-8. [PMID: 34894954 DOI: 10.1080/14756366.2021.1988945] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
19 Sbravati D, Bonardi A, Bua S, Angeli A, Ferraroni M, Nocentini A, Casnati A, Gratteri P, Sansone F, Supuran CT. Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases Inhibition. Chemistry 2021;:e202103527. [PMID: 34882858 DOI: 10.1002/chem.202103527] [Reference Citation Analysis]
20 Wang X, Feng YL, Zhao XY, An R, Cao C, Guo MB, Zhang R, Wang YX, Hou Z, Guo C. Discovery of novel aminosaccharide-based sulfonamide derivatives as potential carbonic anhydrase II inhibitors. Bioorg Med Chem Lett 2021;53:128420. [PMID: 34728369 DOI: 10.1016/j.bmcl.2021.128420] [Reference Citation Analysis]
21 Mikulová MB, Kružlicová D, Pecher D, Petreni A, Supuran CT, Mikuš P. Synthesis and Inhibition Activity Study of Triazinyl-Substituted Amino(alkyl)-benzenesulfonamide Conjugates with Polar and Hydrophobic Amino Acids as Inhibitors of Human Carbonic Anhydrases I, II, IV, IX, and XII. Int J Mol Sci 2021;22:11283. [PMID: 34681940 DOI: 10.3390/ijms222011283] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
22 Villegas A, Satheeshkumar R, Ballesteros‐casallas A, Paulino M, Castro A, Espinosa‐bustos C, Salas CO. Convergent synthesis, drug target prediction, and docking studies of new 2,6,9‐trisubstituted purine derivatives. Journal of Heterocyclic Chem 2022;59:97-111. [DOI: 10.1002/jhet.4368] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
23 Supuran CT. Novel carbonic anhydrase inhibitors. Future Med Chem 2021;13:1935-7. [PMID: 34498952 DOI: 10.4155/fmc-2021-0222] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
24 Paul TK, Taraphder S. Molecular modelling of two coordination states of Zn(II) ion at the active site of human carbonic anhydrase II. Chemical Physics 2021;549:111281. [DOI: 10.1016/j.chemphys.2021.111281] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
25 Angeli A, Kartsev V, Petrou A, Pinteala M, Vydzhak RM, Panchishin SY, Brovarets V, De Luca V, Capasso C, Geronikaki A, Supuran CT. New Sulfanilamide Derivatives Incorporating Heterocyclic Carboxamide Moieties as Carbonic Anhydrase Inhibitors. Pharmaceuticals (Basel) 2021;14:828. [PMID: 34451924 DOI: 10.3390/ph14080828] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
26 Supuran CT, Nocentini A, Yakubova E, Savchuk N, Kalinin S, Krasavin M. Biochemical profiling of anti-HIV prodrug Elsulfavirine (Elpida®) and its active form VM1500A against a panel of twelve human carbonic anhydrase isoforms. J Enzyme Inhib Med Chem 2021;36:1056-60. [PMID: 34000969 DOI: 10.1080/14756366.2021.1927007] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
27 Supuran CT. Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders. J Enzyme Inhib Med Chem 2021;36:1702-14. [PMID: 34325588 DOI: 10.1080/14756366.2021.1945049] [Cited by in F6Publishing: 10] [Reference Citation Analysis]
28 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: 6] [Article Influence: 3.0] [Reference Citation Analysis]
29 Nocentini A, Angeli A, Carta F, Winum JY, Zalubovskis R, Carradori S, Capasso C, Donald WA, Supuran CT. Reconsidering anion inhibitors in the general context of drug design studies of modulators of activity of the classical enzyme carbonic anhydrase. J Enzyme Inhib Med Chem 2021;36:561-80. [PMID: 33615947 DOI: 10.1080/14756366.2021.1882453] [Cited by in Crossref: 12] [Cited by in F6Publishing: 44] [Article Influence: 12.0] [Reference Citation Analysis]
30 Angeli A, Urbański LJ, Hytönen VP, Parkkila S, Supuran CT. Activation of the β-carbonic anhydrase from the protozoan pathogen Trichomonas vaginalis with amines and amino acids. J Enzyme Inhib Med Chem 2021;36:758-63. [PMID: 33715570 DOI: 10.1080/14756366.2021.1897802] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
31 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] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
32 Soydan E, Olcay AC, Bilir G, Taş Ö, Şentürk M, Ekinci D, Supuran CT. Investigation of pesticides on honey bee carbonic anhydrase inhibition. J Enzyme Inhib Med Chem 2020;35:1923-7. [PMID: 33078633 DOI: 10.1080/14756366.2020.1835885] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
33 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: 3] [Reference Citation Analysis]
34 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: 44] [Article Influence: 8.0] [Reference Citation Analysis]
35 Mueller SL, Chrysanthopoulos PK, Halili MA, Hepburn C, Nebl T, Supuran CT, Nocentini A, Peat TS, Poulsen SA. The Glitazone Class of Drugs as Carbonic Anhydrase Inhibitors-A Spin-Off Discovery from Fragment Screening. Molecules 2021;26:3010. [PMID: 34070212 DOI: 10.3390/molecules26103010] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
36 Mincione F, Nocentini A, Supuran CT. Advances in the discovery of novel agents for the treatment of glaucoma. Expert Opin Drug Discov 2021;:1-17. [PMID: 33914670 DOI: 10.1080/17460441.2021.1922384] [Cited by in F6Publishing: 8] [Reference Citation Analysis]
37 Nocentini A, Cuffaro D, Ciccone L, Orlandini E, Nencetti S, Nuti E, Rossello A, Supuran CT. Activation of carbonic anhydrases from human brain by amino alcohol oxime ethers: towards human carbonic anhydrase VII selective activators. J Enzyme Inhib Med Chem 2021;36:48-57. [PMID: 33103482 DOI: 10.1080/14756366.2020.1838501] [Cited by in Crossref: 1] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
38 Nocentini A, Capasso C, Supuran CT. Small-molecule CD73 inhibitors for the immunotherapy of cancer: a patent and literature review (2017-present). Expert Opin Ther Pat 2021;:1-10. [PMID: 33909515 DOI: 10.1080/13543776.2021.1923694] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
39 Guglielmi P, Rotondi G, Secci D, Angeli A, Chimenti P, Nocentini A, Bonardi A, Gratteri P, Carradori S, Supuran CT. Novel insights on saccharin- and acesulfame-based carbonic anhydrase inhibitors: design, synthesis, modelling investigations and biological activity evaluation. J Enzyme Inhib Med Chem 2020;35:1891-905. [PMID: 33003975 DOI: 10.1080/14756366.2020.1828401] [Cited by in Crossref: 2] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
40 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: 25] [Article Influence: 11.0] [Reference Citation Analysis]
41 Abutaleb NS, Elhassanny AEM, Flaherty DP, Seleem MN. In vitro and in vivo activities of the carbonic anhydrase inhibitor, dorzolamide, against vancomycin-resistant enterococci. PeerJ 2021;9:e11059. [PMID: 33850651 DOI: 10.7717/peerj.11059] [Cited by in F6Publishing: 9] [Reference Citation Analysis]
42 Mishra CB, Kumari S, Angeli A, Bua S, Mongre RK, Tiwari M, Supuran CT. Discovery of Potent Carbonic Anhydrase Inhibitors as Effective Anticonvulsant Agents: Drug Design, Synthesis, and In Vitro and In Vivo Investigations. J Med Chem 2021;64:3100-14. [PMID: 33721499 DOI: 10.1021/acs.jmedchem.0c01889] [Cited by in Crossref: 3] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
43 Nocentini A, Del Prete S, Mastrolorenzo MD, Donald WA, Capasso C, Supuran CT. Activation studies of the β-carbonic anhydrases from Escherichia coli with amino acids and amines. J Enzyme Inhib Med Chem 2020;35:1379-86. [PMID: 32576029 DOI: 10.1080/14756366.2020.1781845] [Cited by in Crossref: 2] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
44 Thacker PS, Srikanth D, Angeli A, Singh P, Chinchilli KK, Arifuddin M, Supuran CT. Coumarin-Thiourea Hybrids Show Potent Carbonic Anhydrase IX and XIII Inhibitory Action. ChemMedChem 2021;16:1252-6. [PMID: 33346945 DOI: 10.1002/cmdc.202000915] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
45 Oguz M, Kalay E, Akocak S, Nocentini A, Lolak N, Boga M, Yilmaz M, Supuran CT. Synthesis of calix[4]azacrown substituted sulphonamides with antioxidant, acetylcholinesterase, butyrylcholinesterase, tyrosinase and carbonic anhydrase inhibitory action. J Enzyme Inhib Med Chem 2020;35:1215-23. [PMID: 32401067 DOI: 10.1080/14756366.2020.1765166] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 8.0] [Reference Citation Analysis]
46 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: 26] [Article Influence: 9.0] [Reference Citation Analysis]
47 Li L, Cai Y, Sun X, Du X, Jiang Z, Ni H, Yang Y, Chen F. Tyrosinase inhibition by p-coumaric acid ethyl ester identified from camellia pollen. Food Sci Nutr 2021;9:389-400. [PMID: 33473301 DOI: 10.1002/fsn3.2004] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
48 Nada H, Elkamhawy A, Lee K. Structure Activity Relationship of Key Heterocyclic Anti-Angiogenic Leads of Promising Potential in the Fight against Cancer. Molecules 2021;26:553. [PMID: 33494492 DOI: 10.3390/molecules26030553] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
49 Petreni A, De Luca V, Scaloni A, Nocentini A, Capasso C, Supuran CT. Anion inhibition studies of the Zn(II)-bound ι-carbonic anhydrase from the Gram-negative bacterium Burkholderia territorii. J Enzyme Inhib Med Chem 2021;36:372-6. [PMID: 33390061 DOI: 10.1080/14756366.2020.1867122] [Cited by in Crossref: 3] [Cited by in F6Publishing: 14] [Article Influence: 3.0] [Reference Citation Analysis]
50 Urbański LJ, Angeli A, Hytönen VP, Di Fiore A, De Simone G, Parkkila S, Supuran CT. Inhibition of the β-carbonic anhydrase from the protozoan pathogen Trichomonas vaginalis with sulphonamides. J Enzyme Inhib Med Chem 2021;36:329-34. [PMID: 33356653 DOI: 10.1080/14756366.2020.1863958] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
51 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: 5] [Article Influence: 1.5] [Reference Citation Analysis]
52 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: 45] [Article Influence: 9.5] [Reference Citation Analysis]
53 Mansoldo FRP, Carta F, Angeli A, Cardoso VDS, Supuran CT, Vermelho AB. Chagas Disease: Perspectives on the Past and Present and Challenges in Drug Discovery. Molecules 2020;25:E5483. [PMID: 33238613 DOI: 10.3390/molecules25225483] [Cited by in Crossref: 2] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
54 Sever B, Türkeş C, Altıntop MD, Demir Y, Beydemir Ş. Thiazolyl-pyrazoline derivatives: In vitro and in silico evaluation as potential acetylcholinesterase and carbonic anhydrase inhibitors. International Journal of Biological Macromolecules 2020;163:1970-88. [DOI: 10.1016/j.ijbiomac.2020.09.043] [Cited by in Crossref: 15] [Cited by in F6Publishing: 33] [Article Influence: 7.5] [Reference Citation Analysis]
55 Cuffaro D, Nuti E, Rossello A. An overview of carbohydrate-based carbonic anhydrase inhibitors. J Enzyme Inhib Med Chem 2020;35:1906-22. [PMID: 33078634 DOI: 10.1080/14756366.2020.1825409] [Cited by in Crossref: 2] [Cited by in F6Publishing: 10] [Article Influence: 1.0] [Reference Citation Analysis]
56 Luchinat E, Barbieri L, Cremonini M, Nocentini A, Supuran CT, Banci L. Intracellular Binding/Unbinding Kinetics of Approved Drugs to Carbonic Anhydrase II Observed by in-Cell NMR. ACS Chem Biol 2020;15:2792-800. [PMID: 32955851 DOI: 10.1021/acschembio.0c00590] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 9.0] [Reference Citation Analysis]
57 Angeli A, Carta F, Nocentini A, Winum JY, Zalubovskis R, Akdemir A, Onnis V, Eldehna WM, Capasso C, Simone G, Monti SM, Carradori S, Donald WA, Dedhar S, Supuran CT. Carbonic Anhydrase Inhibitors Targeting Metabolism and Tumor Microenvironment. Metabolites 2020;10:E412. [PMID: 33066524 DOI: 10.3390/metabo10100412] [Cited by in Crossref: 28] [Cited by in F6Publishing: 53] [Article Influence: 14.0] [Reference Citation Analysis]
58 Gouyou B, Millul J, Villa A, Cazzamalli S, Neri D, Matasci M. Sortase-Mediated Site-Specific Modification of Interleukin-2 for the Generation of a Tumor-Targeting Acetazolamide-Cytokine Conjugate. ACS Omega 2020;5:26077-83. [PMID: 33073134 DOI: 10.1021/acsomega.0c03592] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
59 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: 6] [Article Influence: 0.5] [Reference Citation Analysis]
60 Costa G, Maruca A, Rocca R, Ambrosio FA, Berrino E, Carta F, Mesiti F, Salatino A, Lanzillotta D, Trapasso F, Artese A, Alcaro S, Supuran CT. In Silico Identification and Biological Evaluation of Antioxidant Food Components Endowed with IX and XII hCA Inhibition. Antioxidants (Basel) 2020;9:E775. [PMID: 32825614 DOI: 10.3390/antiox9090775] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
61 Swain B, Angeli A, Singh P, Supuran CT, Arifuddin M. New coumarin/sulfocoumarin linked phenylacrylamides as selective transmembrane carbonic anhydrase inhibitors: Synthesis and in-vitro biological evaluation. Bioorg Med Chem 2020;28:115586. [PMID: 32631564 DOI: 10.1016/j.bmc.2020.115586] [Cited by in Crossref: 5] [Cited by in F6Publishing: 11] [Article Influence: 2.5] [Reference Citation Analysis]
62 Sanyanga TA, Tastan Bishop Ö. Structural Characterization of Carbonic Anhydrase VIII and Effects of Missense Single Nucleotide Variations to Protein Structure and Function. Int J Mol Sci 2020;21:E2764. [PMID: 32316137 DOI: 10.3390/ijms21082764] [Cited by in Crossref: 4] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
63 Manasa KL, Pujitha S, Sethi A, Mohammed A, Alvala M, Angeli A, Supuran CT. Synthesis and Biological Evaluation of Imidazo[2 ,1-b]Thiazole based Sulfonyl Piperazines as Novel Carbonic Anhydrase II Inhibitors. Metabolites 2020;10:E136. [PMID: 32244413 DOI: 10.3390/metabo10040136] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]