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For: Yamali C, Gul HI, Kazaz C, Levent S, Gulcin I. Synthesis, structure elucidation, and in vitro pharmacological evaluation of novel polyfluoro substituted pyrazoline type sulfonamides as multi-target agents for inhibition of acetylcholinesterase and carbonic anhydrase I and II enzymes. Bioorganic Chemistry 2020;96:103627. [DOI: 10.1016/j.bioorg.2020.103627] [Cited by in Crossref: 21] [Cited by in F6Publishing: 20] [Article Influence: 10.5] [Reference Citation Analysis]
Number Citing Articles
1 Ren S, Jiang S, Yan X, Chen R, Cui H. Challenges and Opportunities: Porous Supports in Carbonic Anhydrase Immobilization. Journal of CO2 Utilization 2020;42:101305. [DOI: 10.1016/j.jcou.2020.101305] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
2 Anil DA, Polat MF, Saglamtas R, Tarikogullari AH, Alagoz MA, Gulcin I, Algul O, Burmaoglu S. Exploring enzyme inhibition profiles of novel halogenated chalcone derivatives on some metabolic enzymes: Synthesis, characterization and molecular modeling studies. Computational Biology and Chemistry 2022;100:107748. [DOI: 10.1016/j.compbiolchem.2022.107748] [Reference Citation Analysis]
3 Haider K, Shafeeque M, Yahya S, Yar MS. A comprehensive review on pyrazoline based heterocyclic hybrids as potent anticancer agents. European Journal of Medicinal Chemistry Reports 2022;5:100042. [DOI: 10.1016/j.ejmcr.2022.100042] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Sepehri N, Mohammadi‐khanaposhtani M, Asemanipoor N, Hosseini S, Biglar M, Larijani B, Mahdavi M, Hamedifar H, Taslimi P, Sadeghian N, Gulcin I. Synthesis, characterization, molecular docking, and biological activities of coumarin–1,2,3‐triazole‐acetamide hybrid derivatives. Arch Pharm 2020;353:2000109. [DOI: 10.1002/ardp.202000109] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
5 Bilginer S, Gul HI, Anil B, Demir Y, Gulcin I. Synthesis and in silico studies of triazene-substituted sulfamerazine derivatives as acetylcholinesterase and carbonic anhydrases inhibitors. Arch Pharm (Weinheim) 2021;354:e2000243. [PMID: 32984993 DOI: 10.1002/ardp.202000243] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Yamali C, GÜl Hİ, Demİr Y, Kazaz C, GÜlÇİn İ. Synthesis and bioactivities of 1-(4-hydroxyphenyl)-2-((heteroaryl)thio)ethanones as carbonic anhydrase I, II and acetylcholinesterase inhibitors. Turk J Chem 2020;44:1058-67. [PMID: 33488212 DOI: 10.3906/kim-2004-36] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
7 Magar P, Parravicini O, Štěpánková Š, Svrčková K, Garro AD, Jendrzejewska I, Pauk K, Hošek J, Jampílek J, Enriz RD, Imramovský A. Novel Sulfonamide-Based Carbamates as Selective Inhibitors of BChE. Int J Mol Sci 2021;22:9447. [PMID: 34502357 DOI: 10.3390/ijms22179447] [Reference Citation Analysis]
8 Ghiasi M, Goli NE, Gholami S, Supuran CT. QM and QM/MM study on inhibition mechanism of polyphenolic compounds as non-classical inhibitors of α-human carbonic anhydrase (II). Theor Chem Acc 2021;140. [DOI: 10.1007/s00214-021-02839-5] [Reference Citation Analysis]
9 Obaid RJ, Naeem N, Mughal EU, Al-rooqi MM, Sadiq A, Jassas RS, Moussa Z, Ahmed SA. Inhibitory potential of nitrogen, oxygen and sulfur containing heterocyclic scaffolds against acetylcholinesterase and butyrylcholinesterase. RSC Adv 2022;12:19764-855. [DOI: 10.1039/d2ra03081k] [Reference Citation Analysis]
10 Qin XJ, Liu H, Li PP, Ni W, He L, Khan A, Hao XJ, Liu HY. Polymethylated acylphloroglucinols from Rhodomyrtus tomentosa exert acetylcholinesterase inhibitory effects. Bioorg Chem 2021;107:104519. [PMID: 33293058 DOI: 10.1016/j.bioorg.2020.104519] [Reference Citation Analysis]
11 Gülçin İ, Trofimov B, Kaya R, Taslimi P, Sobenina L, Schmidt E, Petrova O, Malysheva S, Gusarova N, Farzaliyev V, Sujayev A, Alwasel S, Supuran CT. Synthesis of nitrogen, phosphorus, selenium and sulfur-containing heterocyclic compounds - Determination of their carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase and α-glycosidase inhibition properties. Bioorg Chem 2020;103:104171. [PMID: 32891857 DOI: 10.1016/j.bioorg.2020.104171] [Cited by in Crossref: 20] [Cited by in F6Publishing: 11] [Article Influence: 10.0] [Reference Citation Analysis]
12 Demir-Yazıcı K, Apaydın ÇB, Soylu-Eter Ö, Özsoy N, Karalı N. Synthesis, molecular modeling and cholinesterase inhibitory effects of 2-indolinone-based hydrazinecarbothioamides. Future Med Chem 2021;13:2133-51. [PMID: 34755546 DOI: 10.4155/fmc-2021-0018] [Reference Citation Analysis]
13 Bilginer S, Bardaweel SK, Demir Y, Gulcin I, Kazaz C. Synthesis, cytotoxicities, and carbonic anhydrase inhibition activities of pyrazoline–benzenesulfonamide derivatives harboring phenol/polyphenol moieties. Med Chem Res. [DOI: 10.1007/s00044-022-02893-z] [Reference Citation Analysis]
14 TuĞrak M, GÜl Hİ, Anil B, GÜlÇİn İ. Synthesis and pharmacological effects of novel benzenesulfonamides carrying benzamide moiety as carbonic anhydrase and acetylcholinesterase inhibitors. Turk J Chem 2020;44:1601-9. [PMID: 33488256 DOI: 10.3906/kim-2007-37] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Tugrak M, Gul HI, Demir Y, Gulcin I. Synthesis of benzamide derivatives with thiourea-substituted benzenesulfonamides as carbonic anhydrase inhibitors. Arch Pharm (Weinheim) 2021;354:e2000230. [PMID: 33043495 DOI: 10.1002/ardp.202000230] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Tugrak M, Gul HI, Demir Y, Levent S, Gulcin I. Synthesis and in vitro carbonic anhydrases and acetylcholinesterase inhibitory activities of novel imidazolinone-based benzenesulfonamides. Arch Pharm (Weinheim) 2021;354:e2000375. [PMID: 33283898 DOI: 10.1002/ardp.202000375] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
17 Rana M, Arif R, Khan FI, Maurya V, Singh R, Faizan MI, Yasmeen S, Dar SH, Alam R, Sahu A, Ahmad T, Rahisuddin. Pyrazoline analogs as potential anticancer agents and their apoptosis, molecular docking, MD simulation, DNA binding and antioxidant studies. Bioorg Chem 2021;108:104665. [PMID: 33571809 DOI: 10.1016/j.bioorg.2021.104665] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
18 Wen H, Zhang L, Du Y, Wang Z, Jiang Y, Bian H, Cui J, Jia S. Bimetal based inorganic-carbonic anhydrase hybrid hydrogel membrane for CO2 capture. Journal of CO2 Utilization 2020;39:101171. [DOI: 10.1016/j.jcou.2020.101171] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
19 Nehra B, Rulhania S, Jaswal S, Kumar B, Singh G, Monga V. Recent advancements in the development of bioactive pyrazoline derivatives. Eur J Med Chem 2020;205:112666. [PMID: 32795767 DOI: 10.1016/j.ejmech.2020.112666] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
20 BiLGiNER S, Anil B, Koca M, Demir Y, Gülçin İ. Novel Mannich bases with strong carbonic anhydrases and acetylcholinesterase inhibition effects: 3-(aminomethyl)-6-{3-[4-(trifluoromethyl)phenyl]acryloyl}-2(3H)-benzoxazolones. Turk J Chem 2021;45:805-18. [PMID: 34385868 DOI: 10.3906/kim-2101-25] [Reference Citation Analysis]
21 Artunc T, Menzek A, Taslimi P, Gulcin I, Kazaz C, Sahin E. Synthesis and antioxidant activities of phenol derivatives from 1,6-bis(dimethoxyphenyl)hexane-1,6-dione. Bioorg Chem 2020;100:103884. [PMID: 32388430 DOI: 10.1016/j.bioorg.2020.103884] [Cited by in Crossref: 18] [Cited by in F6Publishing: 13] [Article Influence: 9.0] [Reference Citation Analysis]
22 Aydin T. Secondary metabolites of Helichrysum plicatum DC. subsp. plicatum flowers as strong carbonic anhydrase, cholinesterase and α-glycosidase inhibitors. Z Naturforsch C J Biosci 2020;75:153-9. [PMID: 32383693 DOI: 10.1515/znc-2020-0026] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
23 Ghiasi M, Gholami S. Quantum mechanical study of human carbonic anhydrase II in complex with polyamines as novel inhibitors: Kinetic and thermodynamic investigation. Computational and Theoretical Chemistry 2020;1186:112911. [DOI: 10.1016/j.comptc.2020.112911] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 3.5] [Reference Citation Analysis]
24 Gümüş M, Babacan ŞN, Demir Y, Sert Y, Koca İ, Gülçin İ. Discovery of sulfadrug-pyrrole conjugates as carbonic anhydrase and acetylcholinesterase inhibitors. Arch Pharm (Weinheim) 2021;:e2100242. [PMID: 34609760 DOI: 10.1002/ardp.202100242] [Reference Citation Analysis]
25 Kumar S, Rulhania S, Jaswal S, Monga V. Recent advances in the medicinal chemistry of carbonic anhydrase inhibitors. Eur J Med Chem 2021;209:112923. [PMID: 33121862 DOI: 10.1016/j.ejmech.2020.112923] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
26 Buabeng ER, Henary M. Developments of small molecules as inhibitors for carbonic anhydrase isoforms. Bioorg Med Chem 2021;39:116140. [PMID: 33905966 DOI: 10.1016/j.bmc.2021.116140] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Aksu K, Akincioglu H, Gulcin I, Kelebekli L. Concise syntheses and some biological activities of dl-2,5-di-O-methyl-chiro-inositol, dl-1,4-di-O-methyl-scyllo-inositol, and dl-1,6-dibromo-1,6-dideoxy-2,5-di-O-methyl-chiro-inositol. Arch Pharm (Weinheim) 2021;354:e2000254. [PMID: 32997390 DOI: 10.1002/ardp.202000254] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
28 Türkeş C, Demir Y, Beydemir Ş. Calcium channel blockers: molecular docking and inhibition studies on carbonic anhydrase I and II isoenzymes. Journal of Biomolecular Structure and Dynamics 2021;39:1672-80. [DOI: 10.1080/07391102.2020.1736631] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 8.0] [Reference Citation Analysis]