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For: Supuran CT. Carbonic anhydrase inhibitors: an update on experimental agents for the treatment and imaging of hypoxic tumors. Expert Opin Investig Drugs 2021;:1-12. [PMID: 34865569 DOI: 10.1080/13543784.2021.2014813] [Cited by in Crossref: 16] [Cited by in F6Publishing: 20] [Article Influence: 16.0] [Reference Citation Analysis]
Number Citing Articles
1 De Luca V, Carginale V, Supuran CT, Capasso C. The gram-negative bacterium Escherichia coli as a model for testing the effect of carbonic anhydrase inhibition on bacterial growth. J Enzyme Inhib Med Chem 2022;37:2092-8. [PMID: 35899716 DOI: 10.1080/14756366.2022.2101644] [Reference Citation Analysis]
2 Liguori F, Carradori S, Ronca R, Rezzola S, Filiberti S, Carta F, Turati M, Supuran CT. Benzenesulfonamides with different rigidity-conferring linkers as carbonic anhydrase inhibitors: an insight into the antiproliferative effect on glioblastoma, pancreatic, and breast cancer cells. J Enzyme Inhib Med Chem 2022;37:1857-69. [PMID: 35768159 DOI: 10.1080/14756366.2022.2091557] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
3 Supuran CT. Carbonic Anhydrase Inhibitors from Marine Natural Products. Marine Drugs 2022;20:721. [DOI: 10.3390/md20110721] [Reference Citation Analysis]
4 Agamennone M, Fantacuzzi M, Carradori S, Petzer A, Petzer JP, Angeli A, Supuran CT, Luisi G. Coumarin-Based Dual Inhibitors of Human Carbonic Anhydrases and Monoamine Oxidases Featuring Amino Acyl and (Pseudo)-Dipeptidyl Appendages: In Vitro and Computational Studies. Molecules 2022;27:7884. [DOI: 10.3390/molecules27227884] [Reference Citation Analysis]
5 De Luca V, Giovannuzzi S, Supuran CT, Capasso C. May Sulfonamide Inhibitors of Carbonic Anhydrases from Mammaliicoccus sciuri Prevent Antimicrobial Resistance Due to Gene Transfer to Other Harmful Staphylococci? IJMS 2022;23:13827. [DOI: 10.3390/ijms232213827] [Reference Citation Analysis]
6 Kalyanasundar B, Blonde GD, Spector AC, Travers SP. A T1R-independent mechanism for responses to hyperosmotic sugars involves a carbonic anhydrase-sensitive mechanism in Type III receptor cells.. [DOI: 10.1101/2022.09.16.508275] [Reference Citation Analysis]
7 Thacker PS, Newaskar V, Angeli A, Sigalapalli DK, Goud NS, Chirra H, Shaik AB, Arifuddin M, Supuran CT. Synthesis and biological evaluation of coumarin-thiazole hybrids as selective carbonic anhydrase IX and XII inhibitors. Arch Pharm (Weinheim) 2022;:e2200232. [PMID: 36122182 DOI: 10.1002/ardp.202200232] [Reference Citation Analysis]
8 Manzoor S, Angeli A, Zara S, Carradori S, Rahman MA, Raza MK, Supuran CT, Hoda N. Development of benzene and benzothiazole-sulfonamide analogues as selective inhibitors of the tumor-associated carbonic anhydrase IX. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114793] [Reference Citation Analysis]
9 Rai D, Khatua S, Taraphder S. Structure and Dynamics of the Isozymes II and IX of Human Carbonic Anhydrase. ACS Omega. [DOI: 10.1021/acsomega.2c03356] [Reference Citation Analysis]
10 Moi D, Deplano A, Angeli A, Balboni G, Supuran CT, Onnis V. Synthesis of Sulfonamides Incorporating Piperidinyl-Hydrazidoureido and Piperidinyl-Hydrazidothioureido Moieties and Their Carbonic Anhydrase I, II, IX and XII Inhibitory Activity. Molecules 2022;27:5370. [DOI: 10.3390/molecules27175370] [Reference Citation Analysis]
11 Peña L, Jiménez C, Arancibia R, Angeli A, Supuran CT. Heterobimetallic complexes containing organometallic acylhydrazone ligands as potential inhibitors of human carbonic anhydrases. Journal of Inorganic Biochemistry 2022;232:111814. [DOI: 10.1016/j.jinorgbio.2022.111814] [Reference Citation Analysis]
12 Giovannuzzi S, Capasso C, Nocentini A, Supuran CT. Continued Structural Exploration of Sulfocoumarin as Selective Inhibitor of Tumor-Associated Human Carbonic Anhydrases IX and XII. Molecules 2022;27:4076. [DOI: 10.3390/molecules27134076] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Ewies EF, Sabry E, Bekheit MS, Fouad MA, Vullo D, Supuran CT. Click chemistry-based synthesis of new benzenesulfonamide derivatives bearing triazole ring as selective carbonic anhydrase II inhibitors. Drug Dev Res 2022. [PMID: 35706360 DOI: 10.1002/ddr.21957] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
14 Nerella SG, Singh P, Arifuddin M, Supuran CT. Anticancer carbonic anhydrase inhibitors: a patent and literature update 2018-2022. Expert Opin Ther Pat 2022. [PMID: 35616541 DOI: 10.1080/13543776.2022.2083502] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
15 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]
16 Denner TC, Hoenke S, Kraft O, Deigner H, Al-harrasi A, Csuk R. Hydroxyethylamide substituted triterpenoic acids hold good cytotoxicity for human tumor cells. Results in Chemistry 2022. [DOI: 10.1016/j.rechem.2022.100371] [Reference Citation Analysis]
17 Chinchilli KK, Royyala VN, Thacker PS, Angeli A, Danaboina S, Singh P, Nanduri S, Supuran CT, Arifuddin M. Design, synthesis, SAR, and biological evaluation of saccharin-based hybrids as carbonic anhydrase inhibitors. Arch Pharm (Weinheim) 2022;:e2200019. [PMID: 35484599 DOI: 10.1002/ardp.202200019] [Reference Citation Analysis]
18 Tawfik HO, Shaldam MA, Nocentini A, Salem R, Almahli H, Al-Rashood ST, Supuran CT, Eldehna WM. Novel 3-(6-methylpyridin-2-yl)coumarin-based chalcones as selective inhibitors of cancer-related carbonic anhydrases IX and XII endowed with anti-proliferative activity. J Enzyme Inhib Med Chem 2022;37:1043-52. [PMID: 35437108 DOI: 10.1080/14756366.2022.2056734] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
19 Bonardi A, Bua S, Combs J, Lomelino C, Andring J, Osman SM, Toti A, Di Cesare Mannelli L, Gratteri P, Ghelardini C, Mckenna R, Nocentini A, Supuran CT. The three-tails approach as a new strategy to improve selectivity of action of sulphonamide inhibitors against tumour-associated carbonic anhydrase IX and XII. Journal of Enzyme Inhibition and Medicinal Chemistry 2022;37:930-9. [DOI: 10.1080/14756366.2022.2053526] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
20 Mustafa M, Winum JY. The importance of sulfur-containing motifs in drug design and discovery. Expert Opin Drug Discov 2022;:1-12. [PMID: 35193437 DOI: 10.1080/17460441.2022.2044783] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
21 Aspatwar A, Tolvanen MEE, Barker H, Syrjänen L, Valanne S, Purmonen S, Waheed A, Sly WS, Parkkila S. Carbonic Anhydrases in Metazoan Model Organisms: Molecules, Mechanisms, and Physiology. Physiol Rev 2022. [PMID: 35166161 DOI: 10.1152/physrev.00018.2021] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 7.0] [Reference Citation Analysis]
22 Giovannuzzi S, De Luca V, Nocentini A, Capasso C, Supuran CT. Coumarins inhibit η-class carbonic anhydrase from Plasmodium falciparum. J Enzyme Inhib Med Chem 2022;37:680-5. [PMID: 35139744 DOI: 10.1080/14756366.2022.2036986] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
23 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]
24 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]
25 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 Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]