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For: 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]
Number Citing Articles
1 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]
2 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]
3 Rubab L, Afroz S, Ahmad S, Hussain S, Nawaz I, Irfan A, Batool F, Kotwica-Mojzych K, Mojzych M. An Update on Synthesis of Coumarin Sulfonamides as Enzyme Inhibitors and Anticancer Agents. Molecules 2022;27:1604. [PMID: 35268704 DOI: 10.3390/molecules27051604] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
4 Yu JH, Yu ZP, Capon RJ, Zhang H. Natural Enantiomers: Occurrence, Biogenesis and Biological Properties. Molecules 2022;27:1279. [PMID: 35209066 DOI: 10.3390/molecules27041279] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
5 Pan Y, Liu T, Wang X, Sun J. Research progress of coumarins and their derivatives in the treatment of diabetes. Journal of Enzyme Inhibition and Medicinal Chemistry 2022;37:616-28. [DOI: 10.1080/14756366.2021.2024526] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Eldehna WM, Taghour MS, Al-Warhi T, Nocentini A, Elbadawi MM, Mahdy HA, Abdelrahman MA, Alotaibi OJ, Aljaeed N, Elimam DM, Afarinkia K, Abdel-Aziz HA, Supuran CT. Discovery of 2,4-thiazolidinedione-tethered coumarins as novel selective inhibitors for carbonic anhydrase IX and XII isoforms. J Enzyme Inhib Med Chem 2022;37:531-41. [PMID: 34991416 DOI: 10.1080/14756366.2021.2024528] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
7 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]
8 Queen A, Bhutto HN, Yousuf M, Syed MA, Hassan MI. Carbonic anhydrase IX: A tumor acidification switch in heterogeneity and chemokine regulation. Semin Cancer Biol 2022:S1044-579X(22)00001-3. [PMID: 34998944 DOI: 10.1016/j.semcancer.2022.01.001] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 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]
10 Fuentes-Aguilar A, Merino-Montiel P, Montiel-Smith S, Meza-Reyes S, Vega-Báez JL, Puerta A, Fernandes MX, Padrón JM, Petreni A, Nocentini A, Supuran CT, López Ó, Fernández-Bolaños JG. 2-Aminobenzoxazole-appended coumarins as potent and selective inhibitors of tumour-associated carbonic anhydrases. J Enzyme Inhib Med Chem 2022;37:168-77. [PMID: 34894971 DOI: 10.1080/14756366.2021.1998026] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
11 Singh P, Kumar Sigalapalli D, Sridhar Goud N, Swain B, Kumar Sahoo S, Angeli A, Shaik AB, Madhavi Yaddanapudi V, Supuran CT, Arifuddin M. Ureidosulfocoumarin Derivatives As Selective and Potent Carbonic Anhydrase IX and XII Inhibitors. ChemMedChem 2021;:e202100725. [PMID: 34898017 DOI: 10.1002/cmdc.202100725] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Angeli A, Berrino E, Carradori S, Supuran CT, Cirri M, Carta F, Costantino G. Amine- and Amino Acid-Based Compounds as Carbonic Anhydrase Activators. Molecules 2021;26:7331. [PMID: 34885917 DOI: 10.3390/molecules26237331] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
13 Akpunar C, Özdemir N, Karataş MO, Alıcı B, Özdemir İ. Synthesis, crystal structures and catalytic activities of palladium complexes with coumarin-functionalised N-heterocyclic carbene ligands. Inorganic Chemistry Communications 2021;131:108755. [DOI: 10.1016/j.inoche.2021.108755] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
14 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]
15 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]
16 Meleddu R, Deplano S, Maccioni E, Ortuso F, Cottiglia F, Secci D, Onali A, Sanna E, Angeli A, Angius R, Alcaro S, Supuran CT, Distinto S. Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives. J Enzyme Inhib Med Chem 2021;36:685-92. [PMID: 33602041 DOI: 10.1080/14756366.2021.1887171] [Cited by in Crossref: 1] [Cited by in F6Publishing: 9] [Article Influence: 1.0] [Reference Citation Analysis]
17 Miao Y, Yang J, Yun Y, Sun J, Wang X. Synthesis and anti-rheumatoid arthritis activities of 3-(4-aminophenyl)-coumarin derivatives. J Enzyme Inhib Med Chem 2021;36:450-61. [PMID: 33557646 DOI: 10.1080/14756366.2021.1873978] [Cited by in Crossref: 1] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
18 Zhu H, Ying S, Zhou B, Hu X, Liang X, Li W, Wang D, Jin H, Pan Y. Design, synthesis, and evaluation of novel coumarin-dithiocarbamate derivatives (IDs) as anti-colorectal cancer agents. J Enzyme Inhib Med Chem 2021;36:593-604. [PMID: 33557648 DOI: 10.1080/14756366.2021.1875458] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
19 Kuzu B, Tan M, Gülçin İ, Menges N. A novel class for carbonic anhydrases inhibitors and evaluation of their non-zinc binding. Arch Pharm (Weinheim) 2021;:e2100188. [PMID: 34096646 DOI: 10.1002/ardp.202100188] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
20 Montanari S, Allarà M, Scalvini L, Kostrzewa M, Belluti F, Gobbi S, Naldi M, Rivara S, Bartolini M, Ligresti A, Bisi A, Rampa A. New Coumarin Derivatives as Cholinergic and Cannabinoid System Modulators. Molecules 2021;26:3254. [PMID: 34071439 DOI: 10.3390/molecules26113254] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
21 Peerzada MN, Hamel E, Bai R, Supuran CT, Azam A. Deciphering the key heterocyclic scaffolds in targeting microtubules, kinases and carbonic anhydrases for cancer drug development. Pharmacol Ther 2021;225:107860. [PMID: 33895188 DOI: 10.1016/j.pharmthera.2021.107860] [Cited by in F6Publishing: 8] [Reference Citation Analysis]
22 Thacker PS, Tiwari PL, Angeli A, Srikanth D, Swain B, Arifuddin M, Supuran CT. Synthesis and Biological Evaluation of Coumarin-Linked 4-Anilinomethyl-1,2,3-Triazoles as Potent Inhibitors of Carbonic Anhydrases IX and XIII Involved in Tumorigenesis. Metabolites 2021;11:225. [PMID: 33917033 DOI: 10.3390/metabo11040225] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
23 Cakmak EB, Zengin Kurt B, Ozturk Civelek D, Angeli A, Akdemir A, Sonmez F, Supuran CT, Kucukislamoglu M. Quinoline-sulfamoyl carbamates/sulfamide derivatives: Synthesis, cytotoxicity, carbonic anhydrase activity, and molecular modelling studies. Bioorg Chem 2021;110:104778. [PMID: 33684713 DOI: 10.1016/j.bioorg.2021.104778] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
24 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]
25 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]