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For: Gülçin İ, Scozzafava A, Supuran CT, Akıncıoğlu H, Koksal Z, Turkan F, Alwasel S. The effect of caffeic acid phenethyl ester (CAPE) on metabolic enzymes including acetylcholinesterase, butyrylcholinesterase, glutathione S-transferase, lactoperoxidase, and carbonic anhydrase isoenzymes I, II, IX, and XII. Journal of Enzyme Inhibition and Medicinal Chemistry 2016;31:1095-101. [DOI: 10.3109/14756366.2015.1094470] [Cited by in Crossref: 82] [Cited by in F6Publishing: 72] [Article Influence: 11.7] [Reference Citation Analysis]
Number Citing Articles
1 Taslimi P, Turhan K, Türkan F, Sedef Karaman H, Turgut Z, Gulcin İ. Cholinesterases, α-glycosidase, and carbonic anhydrase inhibition properties of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione derivatives: Synthetic analogues for the treatment of Alzheimer's disease and diabetes mellitus. Bioorganic Chemistry 2020;97:103647. [DOI: 10.1016/j.bioorg.2020.103647] [Cited by in Crossref: 26] [Cited by in F6Publishing: 17] [Article Influence: 13.0] [Reference Citation Analysis]
2 Kocyigit UM, Taslimi P, Gezegen H, Gulçin İ, Ceylan M. Evaluation of acetylcholinesterase and carbonic anhydrase inhibition profiles of 1,2,3,4,6-pentasubstituted-4-hydroxy-cyclohexanes: Kocyigit et al. J Biochem Mol Toxicol 2017;31:e21938. [DOI: 10.1002/jbt.21938] [Cited by in Crossref: 40] [Cited by in F6Publishing: 36] [Article Influence: 8.0] [Reference Citation Analysis]
3 D'Ambrosio K, Carradori S, Cesa S, Angeli A, Monti SM, Supuran CT, De Simone G. Catechols: a new class of carbonic anhydrase inhibitors. Chem Commun (Camb) 2020;56:13033-6. [PMID: 33000794 DOI: 10.1039/d0cc05172a] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
4 Yiğit M, Celepci DB, Taslimi P, Yiğit B, Çetinkaya E, Özdemir İ, Aygün M, Gülçin İ. Selenourea and thiourea derivatives of chiral and achiral enetetramines: Synthesis, characterization and enzyme inhibitory properties. Bioorg Chem 2021;120:105566. [PMID: 34974209 DOI: 10.1016/j.bioorg.2021.105566] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Turkan F, Cetin A, Taslimi P, Gulçin İ. Some pyrazoles derivatives: Potent carbonic anhydrase, α-glycosidase, and cholinesterase enzymes inhibitors. Arch Pharm Chem Life Sci 2018;351:1800200. [DOI: 10.1002/ardp.201800200] [Cited by in Crossref: 34] [Cited by in F6Publishing: 31] [Article Influence: 8.5] [Reference Citation Analysis]
6 Türkan F, Huyut Z, Demir Y, Ertaş F, Beydemir Ş. The effects of some cephalosporins on acetylcholinesterase and glutathione S-transferase: an in vivo and in vitro study. Archives of Physiology and Biochemistry 2018;125:235-43. [DOI: 10.1080/13813455.2018.1452037] [Cited by in Crossref: 20] [Cited by in F6Publishing: 18] [Article Influence: 5.0] [Reference Citation Analysis]
7 Köksal Z, Kalin R, Camadan Y, Usanmaz H, Almaz Z, Gülçin İ, Gokcen T, Gören AC, Ozdemir H. Secondary Sulfonamides as Effective Lactoperoxidase Inhibitors. Molecules 2017;22:E793. [PMID: 28538675 DOI: 10.3390/molecules22060793] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 4.2] [Reference Citation Analysis]
8 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]
9 Durmaz L, Erturk A, Akyüz M, Polat Kose L, Uc EM, Bingol Z, Saglamtas R, Alwasel S, Gulcin İ. Screening of Carbonic Anhydrase, Acetylcholinesterase, Butyrylcholinesterase, and α-Glycosidase Enzyme Inhibition Effects and Antioxidant Activity of Coumestrol. Molecules 2022;27:3091. [PMID: 35630566 DOI: 10.3390/molecules27103091] [Reference Citation Analysis]
10 Kocyigit UM, Budak Y, Gürdere MB, Tekin Ş, Köprülü TK, Ertürk F, Özcan K, Gülçin İ, Ceylan M. Synthesis, characterization, anticancer, antimicrobial and carbonic anhydrase inhibition profiles of novel (3aR,4S,7R,7aS)-2-(4-((E)-3-(3-aryl)acryloyl) phenyl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione derivatives. Bioorg Chem 2017;70:118-25. [PMID: 28043719 DOI: 10.1016/j.bioorg.2016.12.001] [Cited by in Crossref: 59] [Cited by in F6Publishing: 55] [Article Influence: 9.8] [Reference Citation Analysis]
11 Aslan HE, Demir Y, Özaslan MS, Türkan F, Beydemir Ş, Küfrevioğlu ÖI. The behavior of some chalcones on acetylcholinesterase and carbonic anhydrase activity. Drug and Chemical Toxicology 2019;42:634-40. [DOI: 10.1080/01480545.2018.1463242] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 5.0] [Reference Citation Analysis]
12 Aras A, Türkan F, Yildiko U, Atalar MN, Kılıç Ö, Alma MH, Bursal E. Biochemical constituent, enzyme inhibitory activity, and molecular docking analysis of an endemic plant species, Thymus migricus. Chem Pap 2021;75:1133-46. [DOI: 10.1007/s11696-020-01375-z] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
13 Türkan F, Huyut Z, Taslimi P, Huyut MT, Gülçin İ. Investigation of the effects of cephalosporin antibiotics on glutathione S-transferase activity in different tissues of rats in vivo conditions in order to drug development research. Drug and Chemical Toxicology 2020;43:423-8. [DOI: 10.1080/01480545.2018.1497644] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 3.5] [Reference Citation Analysis]
14 Ceylan M, Kocyigit UM, Usta NC, Gürbüzlü B, Temel Y, Alwasel SH, Gülçin İ. Synthesis, carbonic anhydrase I and II isoenzymes inhibition properties, and antibacterial activities of novel tetralone-based 1,4-benzothiazepine derivatives: CEYLAN ET AL. J Biochem Mol Toxicol 2017;31:e21872. [DOI: 10.1002/jbt.21872] [Cited by in Crossref: 32] [Cited by in F6Publishing: 24] [Article Influence: 5.3] [Reference Citation Analysis]
15 Bounegru AV, Apetrei C. Voltamperometric Sensors and Biosensors Based on Carbon Nanomaterials Used for Detecting Caffeic Acid-A Review. Int J Mol Sci 2020;21:E9275. [PMID: 33291758 DOI: 10.3390/ijms21239275] [Cited by in Crossref: 4] [Article Influence: 2.0] [Reference Citation Analysis]
16 Kaya R, Taslimi P, Naldan ME, Gulçin İ. The Impacts of Some Sedative Drugs on α -Glycosidase, Acetylcholinesterase and Butyrylcholinesterase Enzymes-potential Drugs for Some Metabolic Diseases. LDDD 2019;16:592-6. [DOI: 10.2174/1570180815666180924110023] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
17 Huyut Z, Alp HH, Yaman T, Keleş ÖF, Yener Z, Türkan F, Ayengin K. Comparison of the protective effects of curcumin and caffeic acid phenethyl ester against doxorubicin-induced testicular toxicity. Andrologia 2020;:e13919. [PMID: 33289171 DOI: 10.1111/and.13919] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
18 Turhan K, Pektaş B, Türkan F, Tuğcu FT, Turgut Z, Taslimi P, Karaman HS, Gulcin I. Novel benzo[ b ]xanthene derivatives: Bismuth(III) triflate‐catalyzed one‐pot synthesis, characterization, and acetylcholinesterase, glutathione S‐transferase, and butyrylcholinesterase inhibitory properties. Arch Pharm 2020;353:2000030. [DOI: 10.1002/ardp.202000030] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
19 Türkan F, Huyut Z, Atalar MN. The toxicological impact of some avermectins on human erythrocytes glutathione S-transferase enzyme: TÜRKAN et al.. J Biochem Mol Toxicol 2018;32:e22205. [DOI: 10.1002/jbt.22205] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 4.5] [Reference Citation Analysis]
20 Al-solami HM. Larvicidal activity of plant extracts by inhibition of detoxification enzymes in Culex pipiens. Journal of King Saud University - Science 2021;33:101371. [DOI: 10.1016/j.jksus.2021.101371] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
21 Atatreh N, Al Rawashdah S, Al Neyadi SS, Abuhamdah SM, Ghattas MA. Discovery of new butyrylcholinesterase inhibitors via structure-based virtual screening. J Enzyme Inhib Med Chem 2019;34:1373-9. [PMID: 31347933 DOI: 10.1080/14756366.2019.1644329] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
22 Türkan F. Investigation of the toxicological and inhibitory effects of some benzimidazole agents on acetylcholinesterase and butyrylcholinesterase enzymes. Arch Physiol Biochem 2021;127:97-101. [PMID: 31135232 DOI: 10.1080/13813455.2019.1618341] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 3.3] [Reference Citation Analysis]
23 Almaz Z, Oztekin A, Abul N, Gerni S, Erel D, Kocak SM, Sengül ME, Ozdemir H. A new approach for affinity-based purification of horseradish peroxidase. Biotechnol Appl Biochem 2021;68:102-13. [PMID: 32060967 DOI: 10.1002/bab.1899] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
24 Mollica A, Locatelli M, Macedonio G, Carradori S, Sobolev AP, De Salvador RF, Monti SM, Buonanno M, Zengin G, Angeli A, Supuran CT. Microwave-assisted extraction, HPLC analysis, and inhibitory effects on carbonic anhydrase I, II, VA, and VII isoforms of 14 blueberry Italian cultivars. Journal of Enzyme Inhibition and Medicinal Chemistry 2016;31:1-6. [DOI: 10.1080/14756366.2016.1214951] [Cited by in Crossref: 39] [Cited by in F6Publishing: 34] [Article Influence: 6.5] [Reference Citation Analysis]
25 Kazancı A, Gök Y, Kaya R, Aktaş A, Taslimi P, Gülçin İ. Synthesis, characterization and bioactivities of dative donor ligand N-heterocyclic carbene (NHC) precursors and their Ag(I)NHC coordination compounds. Polyhedron 2021;193:114866. [DOI: 10.1016/j.poly.2020.114866] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 11.0] [Reference Citation Analysis]
26 Uppugunduri CRS, Muthukumaran J, Robin S, Santos-Silva T, Ansari M. In silico and in vitro investigations on the protein-protein interactions of glutathione S-transferases with mitogen-activated protein kinase 8 and apoptosis signal-regulating kinase 1. J Biomol Struct Dyn 2020;:1-11. [PMID: 32996404 DOI: 10.1080/07391102.2020.1827036] [Reference Citation Analysis]
27 Boztas M, Taslimi P, Yavari MA, Gulcin I, Sahin E, Menzek A. Synthesis and biological evaluation of bromophenol derivatives with cyclopropyl moiety: Ring opening of cyclopropane with monoester. Bioorg Chem 2019;89:103017. [PMID: 31174041 DOI: 10.1016/j.bioorg.2019.103017] [Cited by in Crossref: 56] [Cited by in F6Publishing: 47] [Article Influence: 18.7] [Reference Citation Analysis]
28 Buldurun K, Turan N, Bursal E, Mantarcı A, Turkan F, Taslimi P, Gülçin İ. Synthesis, spectroscopic properties, crystal structures, antioxidant activities and enzyme inhibition determination of Co(II) and Fe(II) complexes of Schiff base. Res Chem Intermed 2020;46:283-97. [DOI: 10.1007/s11164-019-03949-3] [Cited by in Crossref: 16] [Cited by in F6Publishing: 7] [Article Influence: 5.3] [Reference Citation Analysis]
29 Topal M. The inhibition profile of sesamol against α-glycosidase and acetylcholinesterase enzymes. International Journal of Food Properties 2019;22:1527-35. [DOI: 10.1080/10942912.2019.1656234] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
30 Altundas A, Gül B, Çankaya M, Atasever A, Gülçin İ. Synthesis of 2-amino-3-cyanopyridine derivatives and investigation of their carbonic anhydrase inhibition effects. J Biochem Mol Toxicol 2017;31:e21998. [DOI: 10.1002/jbt.21998] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.4] [Reference Citation Analysis]
31 Türkan F, Huyut Z, Basbugan Y, Gülçin İ. Influence of some β-lactam drugs on selected antioxidant enzyme and lipid peroxidation levels in different rat tissues. Drug Chem Toxicol 2020;43:27-36. [PMID: 31060396 DOI: 10.1080/01480545.2019.1608230] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
32 Buldurun K, Turan N, Aras A, Mantarcı A, Turkan F, Bursal E. Spectroscopic and Structural Characterization, Enzyme Inhibitions, and Antioxidant Effects of New Ru(II) and Ni(II) Complexes of Schiff Base. C&B 2019;16. [DOI: 10.1002/cbdv.201900243] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.7] [Reference Citation Analysis]
33 Aksu K, Özgeriş B, Taslimi P, Naderi A, Gülçin İ, Göksu S. Antioxidant Activity, Acetylcholinesterase, and Carbonic Anhydrase Inhibitory Properties of Novel Ureas Derived from Phenethylamines: Biological Activities of Some Novel Urea Derivatives. Arch Pharm Chem Life Sci 2016;349:944-54. [DOI: 10.1002/ardp.201600183] [Cited by in Crossref: 101] [Cited by in F6Publishing: 86] [Article Influence: 16.8] [Reference Citation Analysis]
34 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]
35 Zulhendri F, Perera CO, Tandean S. Can Propolis Be a Useful Adjuvant in Brain and Neurological Disorders and Injuries? A Systematic Scoping Review of the Latest Experimental Evidence. Biomedicines 2021;9:1227. [PMID: 34572413 DOI: 10.3390/biomedicines9091227] [Reference Citation Analysis]
36 Amanat M, Reza MS, Shuvo MSR, Ahmed KS, Hossain H, Tawhid M, Saifuzzaman M, Islam MS, Mazumder T, Islam MA, Daula AFMSU. Zingiber roseum Rosc. rhizome: A rich source of hepatoprotective polyphenols. Biomed Pharmacother 2021;139:111673. [PMID: 33965729 DOI: 10.1016/j.biopha.2021.111673] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
37 Topal F. Inhibition profiles of Voriconazole against acetylcholinesterase, α-glycosidase, and human carbonic anhydrase I and II isoenzymes. J Biochem Mol Toxicol 2019;33:e22385. [PMID: 31478295 DOI: 10.1002/jbt.22385] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
38 Turan B, Şendil K, Şengül E, Gültekin MS, Taslimi P, Gulçin İ, Supuran CT. The synthesis of some β-lactams and investigation of their metal-chelating activity, carbonic anhydrase and acetylcholinesterase inhibition profiles. Journal of Enzyme Inhibition and Medicinal Chemistry 2016;31:79-88. [DOI: 10.3109/14756366.2016.1170014] [Cited by in Crossref: 72] [Cited by in F6Publishing: 63] [Article Influence: 12.0] [Reference Citation Analysis]
39 Zhang L, Qu Z, Song A, Yang J, Yu J, Zhang W, Zhuang C. Garlic oil blocks tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis by inducing phase II drug-metabolizing enzymes. Food Chem Toxicol 2021;157:112581. [PMID: 34562529 DOI: 10.1016/j.fct.2021.112581] [Reference Citation Analysis]
40 Burmaoglu S, Kazancioglu EA, Kazancioglu MZ, Sağlamtaş R, Yalcin G, Gulcin I, Algul O. Synthesis, molecular docking and some metabolic enzyme inhibition properties of biphenyl-substituted chalcone derivatives. Journal of Molecular Structure 2022;1254:132358. [DOI: 10.1016/j.molstruc.2022.132358] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
41 Öztaskın N, Taslimi P, Maraş A, Gülcin İ, Göksu S. Novel antioxidant bromophenols with acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase inhibitory actions. Bioorganic Chemistry 2017;74:104-14. [DOI: 10.1016/j.bioorg.2017.07.010] [Cited by in Crossref: 97] [Cited by in F6Publishing: 85] [Article Influence: 19.4] [Reference Citation Analysis]
42 Türkan F, Huyut Z, Huyut MT, Calimli MH. In vivo biochemical evaluations of some β-lactam group antibiotics on glutathione reductase and glutathione S- transferase enzyme activities. Life Sciences 2019;231:116572. [DOI: 10.1016/j.lfs.2019.116572] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
43 Turkan F, Harbi Calimli M, Akgun A, Gulbagca F, Sen F. Toxicological effects of some antiparasitic drugs on equine liver glutathione S-Transferase enzyme activity. J Pharm Biomed Anal 2020;180:113048. [PMID: 31887670 DOI: 10.1016/j.jpba.2019.113048] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
44 Taslimi P, Sujayev A, Garibov E, Nazarov N, Huyut Z, Alwasel SH, Gulçin İ. Synthesis of new cyclic thioureas and evaluation of their metal-chelating activity, acetylcholinesterase, butyrylcholinesterase, and carbonic anhydrase inhibition profiles: TASLIMI ET AL. J Biochem Mol Toxicol 2017;31:e21897. [DOI: 10.1002/jbt.21897] [Cited by in Crossref: 50] [Cited by in F6Publishing: 49] [Article Influence: 10.0] [Reference Citation Analysis]
45 Ceylan H, Demir Y, Beydemir Ş. Inhibitory Effects of Usnic and Carnosic Acid on Some Metabolic Enzymes: An In vitro Study. PPL 2019;26:364-70. [DOI: 10.2174/0929866526666190301115122] [Cited by in Crossref: 26] [Cited by in F6Publishing: 20] [Article Influence: 8.7] [Reference Citation Analysis]
46 Taslimi P, Işık M, Türkan F, Durgun M, Türkeş C, Gülçin İ, Beydemir Ş. Benzenesulfonamide derivatives as potent acetylcholinesterase, α-glycosidase, and glutathione S-transferase inhibitors: biological evaluation and molecular docking studies. Journal of Biomolecular Structure and Dynamics 2021;39:5449-60. [DOI: 10.1080/07391102.2020.1790422] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
47 Chen L, Cao H, Xiao J. Polyphenols. Polyphenols: Properties, Recovery, and Applications. Elsevier; 2018. pp. 45-67. [DOI: 10.1016/b978-0-12-813572-3.00002-6] [Cited by in Crossref: 18] [Cited by in F6Publishing: 1] [Article Influence: 4.5] [Reference Citation Analysis]
48 Şahin İ, Bingöl Z, Onur S, Güngör SA, Köse M, Gülçin İ, Tümer F. Enzyme Inhibition Properties and Molecular Docking Studies of 4-Sulfonate Containing Aryl α-Hydroxyphosphonates Based Hybrid Molecules. Chem Biodivers 2022;19:e202100787. [PMID: 35315972 DOI: 10.1002/cbdv.202100787] [Reference Citation Analysis]
49 Gokcen T, Gulcin I, Ozturk T, Goren AC. A class of sulfonamides as carbonic anhydrase I and II inhibitors. J Enzyme Inhib Med Chem 2016;31:180-8. [PMID: 27353698 DOI: 10.1080/14756366.2016.1198900] [Cited by in Crossref: 26] [Cited by in F6Publishing: 25] [Article Influence: 4.3] [Reference Citation Analysis]
50 Obaid RJ, Mughal EU, Naeem N, Al-rooqi MM, Sadiq A, Jassas RS, Moussa Z, Ahmed SA. Pharmacological significance of nitrogen-containing five and six-membered heterocyclic scaffolds as potent cholinesterase inhibitors for drug discovery. Process Biochemistry 2022;120:250-9. [DOI: 10.1016/j.procbio.2022.06.009] [Reference Citation Analysis]
51 Türkan F, Taslimi P, Saltan FZ. Tannic acid as a natural antioxidant compound: Discovery of a potent metabolic enzyme inhibitor for a new therapeutic approach in diabetes and Alzheimer's disease. J Biochem Mol Toxicol 2019;33:e22340. [PMID: 30974029 DOI: 10.1002/jbt.22340] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 7.0] [Reference Citation Analysis]
52 Köksal Z, Kalın R, Gerni S, Gülçin İ, Özdemir H. The inhibition effects of some natural products on lactoperoxidase purified from bovine milk: KÖKSAL ET AL. J Biochem Mol Toxicol 2017;31:e21939. [DOI: 10.1002/jbt.21939] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 1.6] [Reference Citation Analysis]
53 Atmaca U, Yıldırım A, Taslimi P, Çelik ST, Gülçin İ, Supuran CT, Çelik M. Intermolecular amination of allylic and benzylic alcohols leads to effective inhibitions of acetylcholinesterase enzyme and carbonic anhydrase I and II isoenzymes. J Biochem Mol Toxicol 2018;32:e22173. [DOI: 10.1002/jbt.22173] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 6.3] [Reference Citation Analysis]
54 Vasudhevan P, Manikandan M, Thangavel P, Vadivukkarasi S. Characterization of partially purified alkaloids from Cucurbita maxima seed and evaluation of their antioxidant activity in human erythrocytes and leukocytes. J Food Biochem 2020;44:e13225. [PMID: 32301513 DOI: 10.1111/jfbc.13225] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
55 Daryadel S, Atmaca U, Taslimi P, Gülçin İ, Çelik M. Novel sulfamate derivatives of menthol: Synthesis, characterization, and cholinesterases and carbonic anhydrase enzymes inhibition properties. Arch Pharm Chem Life Sci 2018;351:1800209. [DOI: 10.1002/ardp.201800209] [Cited by in Crossref: 25] [Cited by in F6Publishing: 20] [Article Influence: 6.3] [Reference Citation Analysis]
56 Cetin A, Türkan F, Taslimi P, Gulçin İ. Synthesis and characterization of novel substituted thiophene derivatives and discovery of their carbonic anhydrase and acetylcholinesterase inhibition effects. J Biochem Mol Toxicol 2018. [DOI: 10.1002/jbt.22261] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
57 Kalin R, Köksal Z, Bayrak S, Gerni S, Ozyürek IN, Usanmaz H, Karaman M, Atasever A, Özdemir H, Gülçin İ. Molecular docking and inhibition profiles of some antibiotics on lactoperoxidase enzyme purified from bovine milk. J Biomol Struct Dyn 2020;:1-10. [PMID: 32856529 DOI: 10.1080/07391102.2020.1814416] [Reference Citation Analysis]
58 Gießel JM, Loesche A, Csuk R, Serbian I. Caffeic acid phenethyl ester (CAPE)-derivatives act as selective inhibitors of acetylcholinesterase. European Journal of Medicinal Chemistry 2019;177:259-68. [DOI: 10.1016/j.ejmech.2019.05.059] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
59 Türkan F, Aygun A, Şakiroğlu H, Şen F. Glutathione S-Transferase: Purification and Characterization of from Cherry Laurel (Prunus laurocerasus L.) and the Investigation In Vitro Effects of Some Metal Ions and Organic Compounds on Enzyme Activity. BioNanoSci 2019;9:683-91. [DOI: 10.1007/s12668-019-00636-w] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
60 Taslimi P, Gulçin İ. Antidiabetic potential: in vitro inhibition effects of some natural phenolic compounds on α-glycosidase and α-amylase enzymes. J Biochem Mol Toxicol 2017;31:e21956. [DOI: 10.1002/jbt.21956] [Cited by in Crossref: 59] [Cited by in F6Publishing: 51] [Article Influence: 11.8] [Reference Citation Analysis]
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