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For: Lolak N, Akocak S, Bua S, Sanku RKK, Supuran CT. Discovery of new ureido benzenesulfonamides incorporating 1,3,5-triazine moieties as carbonic anhydrase I, II, IX and XII inhibitors. Bioorg Med Chem 2019;27:1588-94. [PMID: 30846402 DOI: 10.1016/j.bmc.2019.03.001] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 5.7] [Reference Citation Analysis]
Number Citing Articles
1 Güller P, Atmaca U, Güller U, Çalışır U, Dursun F. Antibacterial properties and carbonic anhydrase inhibition profiles of azido sulfonyl carbamate derivatives. Future Med Chem 2021;13:1285-99. [PMID: 34075799 DOI: 10.4155/fmc-2020-0387] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Andring JT, Fouch M, Akocak S, Angeli A, Supuran CT, Ilies MA, McKenna R. Structural Basis of Nanomolar Inhibition of Tumor-Associated Carbonic Anhydrase IX: X-Ray Crystallographic and Inhibition Study of Lipophilic Inhibitors with Acetazolamide Backbone. J Med Chem 2020;63:13064-75. [PMID: 33085484 DOI: 10.1021/acs.jmedchem.0c01390] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
3 Sağlık BN, Osmaniye D, Çevik UA, Levent S, Çavuşoğlu BK, Büyükemir O, Nezir D, Karaduman AB, Özkay Y, Koparal AS, Beydemir Ş, Kaplancıklı ZA. Synthesis, characterization and carbonic anhydrase I and II inhibitory evaluation of new sulfonamide derivatives bearing dithiocarbamate. Eur J Med Chem 2020;198:112392. [PMID: 32388113 DOI: 10.1016/j.ejmech.2020.112392] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
4 Onyılmaz M, Koca M, Bonardi A, Degirmenci M, Supuran CT. Isocoumarins: a new class of selective carbonic anhydrase IX and XII inhibitors. Journal of Enzyme Inhibition and Medicinal Chemistry 2022;37:743-8. [DOI: 10.1080/14756366.2022.2041630] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Moreno LM, Quiroga J, Abonia R, Lauria A, Martorana A, Insuasty H, Insuasty B. Synthesis, biological evaluation, and in silico studies of novel chalcone- and pyrazoline-based 1,3,5-triazines as potential anticancer agents. RSC Adv 2020;10:34114-29. [PMID: 35519030 DOI: 10.1039/d0ra06799g] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
6 Maliszewski D, Drozdowska D. Recent Advances in the Biological Activity of s-Triazine Core Compounds. Pharmaceuticals 2022;15:221. [DOI: 10.3390/ph15020221] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
7 Elimam DM, Eldehna WM, Salem R, Bonardi A, Nocentini A, Al-Rashood ST, Elaasser MM, Gratteri P, Supuran CT, Allam HA. Natural inspired ligustrazine-based SLC-0111 analogues as novel carbonic anhydrase inhibitors. Eur J Med Chem 2022;228:114008. [PMID: 34871842 DOI: 10.1016/j.ejmech.2021.114008] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Ponomarenko M, Sharypova E, Drachkova I, Chadaeva I, Arkova O, Podkolodnaya O, Ponomarenko P, Kolchanov N, Savinkova L. Unannotated single nucleotide polymorphisms in the TATA box of erythropoiesis genes show in vitro positive involvements in cognitive and mental disorders. BMC Med Genet 2020;21:165. [PMID: 33092544 DOI: 10.1186/s12881-020-01106-x] [Reference Citation Analysis]
9 Chahal V, Nirwan S, Pathak M, Kakkar R. Identification of potent human carbonic anhydrase IX inhibitors: a combination of pharmacophore modeling, 3D-QSAR, virtual screening and molecular dynamics simulations. J Biomol Struct Dyn 2020;:1-16. [PMID: 33317405 DOI: 10.1080/07391102.2020.1860132] [Reference Citation Analysis]
10 Lolak N, Akocak S, Türkeş C, Taslimi P, Işık M, Beydemir Ş, Gülçin İ, Durgun M. Synthesis, characterization, inhibition effects, and molecular docking studies as acetylcholinesterase, α-glycosidase, and carbonic anhydrase inhibitors of novel benzenesulfonamides incorporating 1,3,5-triazine structural motifs. Bioorganic Chemistry 2020;100:103897. [DOI: 10.1016/j.bioorg.2020.103897] [Cited by in Crossref: 40] [Cited by in F6Publishing: 31] [Article Influence: 20.0] [Reference Citation Analysis]
11 Tekeli Y, Lolak N, Sonmez GD, Tekeli T, Akocak S. Antibacterial, Antioxidant and DNA Cleavage Activity Evaluation of Substituted Phenylureido Sulfaguanidine and Sulfamethazine Derivatives. Pharm Chem J. [DOI: 10.1007/s11094-022-02654-7] [Reference Citation Analysis]
12 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: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Zhao P, Zhou Y, Yu XX, Huang C, Wu YD, Yin G, Wu AX. Iodine-Promoted Multicomponent Synthesis of 2,4-Diamino-1,3,5-triazines. Org Lett 2020;22:8528-32. [PMID: 33047965 DOI: 10.1021/acs.orglett.0c03130] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 5.5] [Reference Citation Analysis]
14 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: 2] [Article Influence: 8.0] [Reference Citation Analysis]
15 Gharat R, Prabhu A, Khambete MP. Potential of triazines in Alzheimer's disease: A versatile privileged scaffold. Archiv der Pharmazie. [DOI: 10.1002/ardp.202100388] [Reference Citation Analysis]
16 Li F, Wang C, Xu Y, Zhao Z, Su J, Luo C, Ning Y, Li Z, Li C, Wang L. Efficient synthesis of unsymmetrical trisubstituted 1,3,5-triazines catalyzed by hemoglobin. Molecular Catalysis 2021;505:111519. [DOI: 10.1016/j.mcat.2021.111519] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
17 Akocak S, Güzel-Akdemir Ö, Kishore Kumar Sanku R, Russom SS, Iorga BI, Supuran CT, Ilies MA. Pyridinium derivatives of 3-aminobenzenesulfonamide are nanomolar-potent inhibitors of tumor-expressed carbonic anhydrase isozymes CA IX and CA XII. Bioorg Chem 2020;103:104204. [PMID: 32891000 DOI: 10.1016/j.bioorg.2020.104204] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
18 Güller P, Dağalan Z, Güller U, Çalışır U, Nişancı B. Enzymes inhibition profiles and antibacterial activities of benzylidenemalononitrile derivatives. Journal of Molecular Structure 2021;1239:130498. [DOI: 10.1016/j.molstruc.2021.130498] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
19 Mondal UK, Doroba K, Shabana AM, Adelberg R, Alam MR, Supuran CT, Ilies MA. PEG Linker Length Strongly Affects Tumor Cell Killing by PEGylated Carbonic Anhydrase Inhibitors in Hypoxic Carcinomas Expressing Carbonic Anhydrase IX. Int J Mol Sci 2021;22:1120. [PMID: 33498779 DOI: 10.3390/ijms22031120] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
20 Hashem HE, Amr AEE, Nossier ES, Anwar MM, Azmy EM. New Benzimidazole-, 1,2,4-Triazole-, and 1,3,5-Triazine-Based Derivatives as Potential EGFRWT and EGFRT790M Inhibitors: Microwave-Assisted Synthesis, Anticancer Evaluation, and Molecular Docking Study. ACS Omega 2022;7:7155-71. [PMID: 35252706 DOI: 10.1021/acsomega.1c06836] [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] [Reference Citation Analysis]
22 Lolak N, Boga M, Tuneg M, Karakoc G, Akocak S, Supuran CT. Sulphonamides incorporating 1,3,5-triazine structural motifs show antioxidant, acetylcholinesterase, butyrylcholinesterase, and tyrosinase inhibitory profile. J Enzyme Inhib Med Chem 2020;35:424-31. [PMID: 31899985 DOI: 10.1080/14756366.2019.1707196] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
23 Guo W, Zhao M, Du C, Zheng L, Li L, Chen L, Tao K, Tan W, Xie Z, Cai L, Fan X, Zhang K. Visible-Light-Catalyzed [3 + 1 + 2] Coupling Annulations for the Synthesis of Unsymmetrical Trisubstituted Amino-1,3,5-triazines. J Org Chem 2019;84:15508-19. [DOI: 10.1021/acs.joc.9b02514] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 4.3] [Reference Citation Analysis]
24 Majeed Ganai A, Khan Pathan T, Hampannavar GA, Pawar C, Obakachi VA, Kushwaha B, Deshwar Kushwaha N, Karpoormath R. Recent Advances on the s‐Triazine Scaffold with Emphasis on Synthesis, Structure‐Activity and Pharmacological Aspects: A Concise Review. ChemistrySelect 2021;6:1616-60. [DOI: 10.1002/slct.202004591] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
25 Mikulová MB, Kružlicová D, Pecher D, Supuran CT, Mikuš P. Synthetic Strategies and Computational Inhibition Activity Study for Triazinyl-Substituted Benzenesulfonamide Conjugates with Polar and Hydrophobic Amino Acids as Inhibitors of Carbonic Anhydrases. Int J Mol Sci 2020;21:E3661. [PMID: 32456080 DOI: 10.3390/ijms21103661] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
26 Chahal V, Nirwan S, Kakkar R. A comparative study of the binding modes of SLC-0111 and its analogues in the hCA II and hCA IX active sites using QM/MM, molecular docking, MM-GBSA and MD approaches. Biophys Chem 2020;265:106439. [PMID: 32738591 DOI: 10.1016/j.bpc.2020.106439] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]