References
- Akıncıoğlu, A., Akıncıoğlu, H., Gülçin, İ., Durdagi, S., Supuran, C., & Göksu, S. (2015). Discovery of potent carbonic anhydrase and acetylcholine esterase inhibitors: Novel sulfamoylcarbamates and sulfamides derived from acetophenones. Bioorganic & Medicinal Chemistry, 23(13), 3592–3602. https://doi.org/https://doi.org/10.1016/j.bmc.2015.04.019
- Aktas, A., Barut Celepci, D., Gok, Y., Taslimi, P., Akincioglu, H., & Gulcin, İ. (2020). A novel Ag-N-heterocyclic carbene complex bearing the hydroxyethyl ligand: Synthesis, characterization, crystal and spectral structures and bioactivity properties. Crystals, 10(3), 171. https://doi.org/https://doi.org/10.3390/cryst10030171
- Atmaca, U., Yıldırım, A., Taslimi, P., Çelik, S., Gülçin, İ., Supuran, C., & Çelik, M. (2018). Intermolecular amination of allylic and benzylic alcohols leads to effective inhibitions of acetylcholinesterase enzyme and carbonic anhydrase I and II isoenzymes. Journal of Biochemical and Molecular Toxicology, 32(8), e22173. https://doi.org/https://doi.org/10.1002/jbt.22173
- Behcet, A., Çağlılar, T., Celepci, D., Aktaş, A., Taslimi, P., Gök, Y., Aygün, M., Kaya, R., & Gülçin, İ. (2018). Synthesis, characterization and crystal structure of 2-(4-hydroxyphenyl)ethyl and 2-(4-nitrophenyl)ethyl substituted benzimidazole bromide salts: Their inhibitory properties against carbonic anhydrase and acetylcholinesterase. Journal of Molecular Structure, 1170, 160–169. https://doi.org/https://doi.org/10.1016/j.molstruc.2018.05.077
- Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72(1–2), 248–254. https://doi.org/https://doi.org/10.1016/0003-2697(76)90527-3
- Burmaoglu, S., Kazancioglu, E. A., Kaya, R., Kazancioglu, M., Karaman, M., Algul, O., & Gulcin, I. (2020). Synthesis of novel organohalogen chalcone derivatives and screening of their molecular docking study and some enzymes inhibition effects. Journal of Molecular Structure, 1208, 127868. https://doi.org/https://doi.org/10.1016/j.molstruc.2020.127868
- Cheung, J., Gary, E., Shiomi, K., & Rosenberry, T. (2013). Structures of human acetylcholinesterase bound to dihydrotanshinone I and territrem B show peripheral site flexibility. ACS Medicinal Chemistry Letters, 4(11), 1091–1096. https://doi.org/https://doi.org/10.1021/ml400304w
- Ekiz, M., Tutar, A., Ökten, S., Bütün, B., Koçyiğit, Ü., Taslimi, P., & Topçu, G. (2018). Synthesis, characterization, and SAR of arylated indenoquinoline-based cholinesterase and carbonic anhydrase inhibitors. Archiv der Pharmazie, 351(9), 1800167. https://doi.org/https://doi.org/10.1002/ardp.201800167
- Ellman, G. L., Courtney, K. D., Andres, V., & Feather-Stone, R. M. (1961). A new and rapid colorimetric determination of acetylcholinesterase activity. Biochemical Pharmacology, 7, 88–95. https://doi.org/https://doi.org/10.1016/0006-2952(61)90145-9
- Ertas, M., Sahin, Z., Bulbul, E., Bender, C., Biltekin, S., Berk, B., Yurttas, L., Nalbur, A., Celik, H., & Demirayak, Ş. (2019). Potent ribonucleotide reductase inhibitors: Thiazole‐containing thiosemicarbazone derivatives. Archiv der Pharmazie, 352(11), 1900033. https://doi.org/https://doi.org/10.1002/ardp.201900033
- Friesner, R., Murphy, R., Repasky, M., Frye, L., Greenwood, J., Halgren, T., Sanschagrin, P., & Mainz, D. (2006). Extra precision Glide: Docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes. Journal of Medicinal Chemistry, 49(21), 6177–6196. https://doi.org/https://doi.org/10.1021/jm051256o
- Frisch, M., Trucks, G., Schlegel, H., Scuseria, G., Robb, M., Cheeseman, J., Scalmani, G., Barone, V., Mennucci, B., Petersson, G., Nakatsuji, H., Caricato, M., Li, X., Hratchian, H., Izmaylov, A., Bloino, J., Zheng, G., Sonnenberg, J., Hada, M., … Fox, D. (2009). Gaussian 09, Revision D.01. Wallingford, CT: Gaussian, Inc.
- Göçer, H., Akincioğlu, A., Göksu, S., Gülçin, İ., & Supuran, C. (2015). Carbonic anhydrase and acetylcholinesterase inhibitory effects of carbamates and sulfamoylcarbamates. Journal of Enzyme Inhibition and Medicinal Chemistry, 30(2), 316–320. https://doi.org/https://doi.org/10.3109/14756366.2014.928704
- Göçer, H., Akıncıoğlu, A., Öztaşkın, N., Göksu, S., & Gülçin, İ. (2013). Synthesis, antioxidant, and antiacetylcholinesterase activities of sulfonamide derivatives of dopamine-related compounds. Archiv der Pharmazie, 346(11), 783–792. https://doi.org/https://doi.org/10.1002/ardp.201300228
- Guillaume, M., Delphine, B., Annie-Claude, G., Jocelyne, L., & Mihaela, G. (2008). Efficient synthesis of primary 2-aminothiols from 2-aminoalcohols and methyldithioacetate. Tetrahedron Letters, 49(46), 6553–6555.
- Gulçin, İ., Taslimi, P., Aygün, A., Sadeghian, N., Bastem, E., Kufrevioglu, O. I., Turkan, F., & Şen, F. (2018). Antidiabetic and antiparasitic potentials: Inhibition effects of some natural antioxidant compounds on α-glycosidase, α-amylase and human glutathione S-transferase enzymes. International Journal of Biological Macromolecules, 119, 741–746. https://doi.org/https://doi.org/10.1016/j.ijbiomac.2018.08.001
- Gulçin, İ., Taslimi, P., Huyut, Z., Safarova, L., Abbasova, M., Farzaliyev, V., Sujayev, A., Alwasel, S., Beydemir, Ş., & Supuran, C. (2017). Synthesis and biological evaluation of aminomethyl and alkoxymethyl derivatives as carbonic anhydrase, acetylcholinesterase and butyrylcholinesterase inhibitors. Journal of Enzyme Inhibition and Medicinal Chemistry, 32(1), 1174–1182. https://doi.org/https://doi.org/10.1080/14756366.2017.1368019
- Gunduz, S., Budama-Kilinc, Y., Cakir-Koc, R., Zorlu, T., Bicak, B., Kokcu, Y., Ozel, A. E., & Akyuz, S. (2020). In silico design of AVP (4-5) peptide and synthesis, characterization and in vitro activity of chitosan nanoparticles. Daru, 28(1), 139–157. https://doi.org/https://doi.org/10.1007/s40199-019-00325-9
- Jayarajan, R., Satheeshkumar, R., Kottha, T., Subbaramanian, S., Sayin, K., & Vasuki, G. (2020). Water mediated synthesis of 6-amino-5-cyano-2-oxo-N-(pyridin-2-yl)-4-(p-tolyl)-2H-[1,2'-bipyridine]-3-carboxamide and 6-amino-5-cyano-4-(4-fluorophenyl)-2-oxo-N-(pyridin-2-yl)-2H-[1,2'-bipyridine]-3-carboxamide - An experimental and computational studies with non-linear optical (NLO) and molecular docking analyses. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 229, 117861. https://doi.org/https://doi.org/10.1016/j.saa.2019.117861
- Jorgensen, W., & Duffy, E. (2002). Prediction of drug solubility from structure. Advanced Drug Delivery Reviews, 54(3), 355–366. https://doi.org/https://doi.org/10.1016/S0169-409X(02)00008-X
- Karimov, A., Orujova, A., Taslimi, P., Sadeghian, N., Mammadov, B., Karaman, H. S., Farzaliyev, V., Sujayev, A., Tas, R., Alwasel, S., & Gulçin, İ. (2020). Novel functionally substituted esters based on sodium diethyldithiocarbamate derivatives: Synthesis, characterization, biological activity and molecular docking studies. Bioorganic Chemistry, 99, 103762. https://doi.org/https://doi.org/10.1016/j.bioorg.2020.103762
- Kocyigit, U., Taşkıran, A., Taslimi, P., Yokuş, A., Temel, Y., & Gulçin, İ. (2017). Inhibitory effects of oxytocin and oxytocin receptor antagonist atosiban on the activities of carbonic anhydrase and acetylcholinesterase enzymes in the liver and kidney tissues of rats. Journal of Biochemical and Molecular Toxicology, 31(11), e21972. https://doi.org/https://doi.org/10.1002/jbt.21972
- Košak, U., Knez, D., Coquelle, N., Brus, B., Pišlar, A., Nachon, F., Brazzolotto, X., Kos, J., Colletier, J. P., & Gobec, S. (2017). N-Propargylpiperidines with naphthalene-2-carboxamide or naphthalene-2-sulfonamide moieties: Potential multifunctional anti-Alzheimer's agents. Bioorganic and Medicinal Chemistry, 25(2), 633–645. https://doi.org/https://doi.org/10.1016/j.bmc.2016.11.032
- Li, Y., Bai, B., Ye, J., Liu, H., Liu, Y., & Zhang, W. (2008). Reviews on preparation and determination of α-glucosidase inhibitor. Food Sciences, 29, 617–619.
- Lineweaver, H., & Burk, D. (1934). The determination of enzyme dissociation constants. Journal of the American Chemical Society, 56(3), 658–666. https://doi.org/https://doi.org/10.1021/ja01318a036
- Lipinski, C., Lombardo, F., Dominy, B., & Feeney, P. (1997). Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Advanced Drug Delivery Reviews, 23(1–3), 3–25. https://doi.org/https://doi.org/10.1016/S0169-409X(96)00423-1
- Maharramov, A., Huseynova, A., Gasımova, Y., Allahverdiyev, M., & Zalov, A. (2017). 1, 2- aminothioly as an anelyticaf reagent for extriction spectrophotometric determination of Copper (II). International Journal of Innovative Science Engineering and Technology, 4, 174–180.
- Maharramov, A., Kurbanova, M., Sadigova, A., Kaya, R., Taslimi, P., Sujayev, A., Farzaliyev, V., & Gulcin, İ. (2019). The synthesis and biological evaluation of optically active 2-amino-4-aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahidro-4H-chromen-3-carbonitriles in the presence of chiral organic catalysts: Antidiabetic and anticholinergics potentials. Archiv der Pharmazie, 352(2), 1800317. https://doi.org/https://doi.org/10.1002/ardp.201800317
- Mamedova, G., Mahmudova, A., Mamedov, S., Erden, Y., Taslimi, P., Tüzün, B., Tas, R., Farzaliyev, V., Sujayev, A., Alwasel, S., & Gulçin, İ. (2019). Novel tribenzylaminobenzolsulphonylimine based on their pyrazine and pyridazines: Synthesis, characterization, antidiabetic, anticancer, anticholinergic, and molecular docking studies. Bioorganic Chemistry, 93, 103313. https://doi.org/https://doi.org/10.1016/j.bioorg.2019.103313
- Mammadov, S., Mahmudova, A., Shakhgeldieva, L., Sujayev, A., Ladokhina, N., Zeynalova, L., & Mammadova, S. (2019). Synthesis and biological activity of new sulfonamides. New Materials, Compounds and Applications, 3, 77–86.
- Massoulié, J., Pezzementi, L., Bon, S., Krejci, E., & Vallette, F. M. (1993). Molecular and cellular biology of cholinesterases. Progress in Neurobiology, 41(1), 31–91. https://doi.org/https://doi.org/10.1016/0301-0082(93)90040-Y
- Sağlık, B., Çavuşoğlu, B., Osmaniye, D., Levent, S., Çevik, U., Ilgın, S., Özkay, Y., Kaplancıklı, Z., & Öztürk, Y. (2019). In vitro and in silico evaluation of new thiazole compounds as monoamine oxidase inhibitors. Bioorganic Chemistry, 85, 97–108. https://doi.org/https://doi.org/10.1016/j.bioorg.2018.12.019
- Sağlık, B., Çevik, U., Osmaniye, D., Levent, S., Çavuşoğlu, B., Demir, Y., Ilgın, S., Özkay, Y., Koparal, A., Beydemir, Ş., & Kaplancıklı, Z. (2019). Synthesis, molecular docking analysis and carbonic anhydrase I-II inhibitory evaluation of new sulfonamide derivatives. Bioorganic Chemistry, 91, 103153. https://doi.org/https://doi.org/10.1016/j.bioorg.2019.103153
- Sastry, G., Adzhigirey, M., Day, T., Annabhimoju, R., & Sherman, W. (2013). Protein and ligand preparation: Parameters, protocols, and influence on virtual screening enrichments. Journal of Computer-Aided Molecular Design, 27(3), 221–234. https://doi.org/https://doi.org/10.1007/s10822-013-9644-8
- Sayin, K., & Karakaş, D. (2017). Determination of structural, spectral, electronic and biological properties of tosufloxacin boron complexes and investigation of substituent effect. Journal of Molecular Structure, 1146, 191–197. https://doi.org/https://doi.org/10.1016/j.molstruc.2017.05.130
- Sayin, K., & Karakaş, D. (2018a). Investigation of structural, electronic properties and docking calculations of some boron complexes with norfloxacin: A computational research. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 202, 276–283. https://doi.org/https://doi.org/10.1016/j.saa.2018.05.055
- Sayin, K., & Karakaş, D. (2018b). Quantum chemical investigation of levofloxacin-boron complexes: A computational approach. Journal of Molecular Structure, 1158, 57–65. https://doi.org/https://doi.org/10.1016/j.molstruc.2018.01.016
- Sayin, K., & Üngördü, A. (2018). Investigation of anticancer properties of caffeinated complexes via computational chemistry methods. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 193, 147–155. https://doi.org/https://doi.org/10.1016/j.saa.2017.12.013
- Sayin, K., & Üngördü, A. (2019). Investigations of structural, spectral and electronic properties of enrofloxacin and boron complexes via quantum chemical calculation and molecular docking. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 220, 117102. https://doi.org/https://doi.org/10.1016/j.saa.2019.05.007
- Schrodinger, L. (2019). Small-Molecule Drug Discovery Suite 2019-4, 2017.
- Schrödinger Release 2020-1. (2020). QikProp, Schrödinger, LLC, New York, NY, 2020.
- Sever, B., Altıntop, M., Özdemir, A., Tabanca, N., Estep, A., Becnel, J., & Bloomquist, J. (2019). Biological evaluation of a series of benzothiazole derivatives as mosquitocidal agents. Open Chemistry, 17(1), 288–294. https://doi.org/https://doi.org/10.1515/chem-2019-0027
- Subhani, S., Jayaraman, A., & Jamil, K. (2015). Homology modelling and molecular docking of MDR1 with chemotherapeutic agents in non-small cell lung cancer. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie, 71, 37–45. https://doi.org/https://doi.org/10.1016/j.biopha.2015.02.009
- Sujayev, A., Maharramova, G., Taslimi, P., Farzaliyev, V., Durmaz, L., & Gulçin, İ. (2018). Synthesis, characterization, antioxidant, antidiabetic, anticholinergic, and anti-epileptic properties of novel N-substituted tetrahydropyrimidines based on phenylthiourea. Journal of Biochemical and Molecular Toxicology, 32(12), e22221. https://doi.org/https://doi.org/10.1002/jbt.22221
- Tan, T., Spadiut, O., Gandini, R., Haltrich, D., & Divne, C. (2014). Structural basis for binding of fluorinated glucose and galactose to trametes multicolor pyranose 2-oxidase variants with improved galactose conversion. PLoS One, 9(1), e86736. https://doi.org/https://doi.org/10.1371/journal.pone.0086736
- Tao, Y., Zhang, Y., Cheng, Y., & Wang, Y. (2013). Rapid screening and identification of α-glucosidase inhibitors from mulberry leaves using enzyme-immobilized magnetic beads coupled with HPLC/MS and NMR. Biomedical Chromatography, 27(2), 148–155. https://doi.org/https://doi.org/10.1002/bmc.2761
- Taslimi, P., Aslan, H. E., Demir, Y., Oztaskin, N., Maraş, A., Gulçin, İ., Beydemir, S., & Goksu, S. (2018). Diarylmethanon, bromophenol and diarylmethane compounds: Discovery of potent aldose reductase, α-amylase and α-glycosidase inhibitors as new therapeutic approach in diabetes and functional hyperglycemia. International Journal of Biological Macromolecules, 119, 857–863. https://doi.org/https://doi.org/10.1016/j.ijbiomac.2018.08.004
- Taslimi, P., Erden, Y., Mamedov, S., Zeynalova, L., Ladokhina, N., Tas, R., Tuzun, B., Sujayev, A., Sadeghian, N., Alwasel, S., & Gulcin, I. (2020). The biological activities, molecular docking studies, and anticancer effects of 1-Arylsuphonylpyrazole derivatives. Journal of Biomolecular Structure and Dynamics. https://doi.org/https://doi.org/10.1080/07391102.2020.1763838.
- Taslimi, P., Sujayev, A., Mamedova, S., Kalın, P., Gulçin, İ., Sadeghian, N., Beydemir, S., Kufrevioglu, O. I., Alwasel, S. H., Farzaliyev, V., & Mamedov, S. (2017). Synthesis and bioactivity of several new hetaryl sulfonamides. Journal of Enzyme Inhibition and Medicinal Chemistry, 32(1), 137–145. https://doi.org/https://doi.org/10.1080/14756366.2016.1238367
- Türkan, F., Huyut, Z., Taslimi, P., & Gülçin, İ. (2018). The in vivo effects of cefazolin, cefuroxime, and cefoperazon on the carbonic anhydrase in different rat tissues. Journal of Biochemical and Molecular Toxicology, 32(3), e22041. https://doi.org/https://doi.org/10.1002/jbt.22041
- Türker, F., Celepci, D., Aktaş, A., Taslimi, P., Gök, Y., Aygün, M., & Gülçin, İ. (2018). Meta-cyanobenzyl substituted benzimidazolium salts: Synthesis, characterization, crystal structure and carbonic anhydrase, α-glycosidase, butyrylcholinesterase, and acetylcholinesterase inhibitory properties. Archiv der Pharmazie, 351(7), 1800029. . https://doi.org/https://doi.org/10.1002/ardp.201800029
- Tüzün, B. (2020). Investi̇gati̇on of pyrazoly derivatives schi̇ff base li̇gands and thei̇r metal complexes used as anti-cancer drug. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 227, 117663https://doi.org/https://doi.org/10.1016/j.saa.2019.117663
- Tüzün, B., & Kaya, C. (2018). Investigation of DNA–RNA molecules for the efficiency and activity of corrosion inhibition by DFT and molecular docking. Journal of Bio-and Tribo-Corrosion, 4, 69.
- Tüzün, B., & Saripinar, E. (2020). Molecular docking and 4D-QSAR model of methanone derivatives by electron conformational-genetic algorithm method. Journal of the Iranian Chemical Society, 17(5), 985–1000. https://doi.org/https://doi.org/10.1007/s13738-019-01835-8
- Üngördü, A., & Sayin, K. (2019). Quantum chemical calculations on sparfloxacin and boron complexes. Chemical Physics Letters, 733, 136677. https://doi.org/https://doi.org/10.1016/j.cplett.2019.136677
- Verpoorte, J. A., Mehta, S., & Edsall, J. T. (1967). Esterase activities of human carbonic anhydrases B and C. Journal of Biological Chemistry, 242, 4221–4229.
- Vijayaraghavan, R., Gautam, A., & Sharma, M. (2009). CHAPTER 60 - Medical countermeasures and other therapeutic strategies for sulfur mustard toxicity. In R. C. Gupta (ed.), Handbook of toxicology of chemical warfare agents (pp. 897–918). New York: Academic Press. https://doi.org/https://doi.org/10.1016/B978-012374484-5.00060-2
- Wang, J.-L., Li, L., Hu, M.-B., Wu, B., Fan, W.-X., Peng, W., Wei, D.-N., & Wu, C.-J. (2019). In silico drug design of inhibitor of nuclear factor kappa B kinase subunit beta inhibitors from 2-acylamino-3-aminothienopyridines based on quantitative structure-activity relationships and molecular docking. Computational Biology and Chemistry, 78, 297–305. https://doi.org/https://doi.org/10.1016/j.compbiolchem.2018.12.021
- Yiğit, B., Yiğit, M., Barut Celepci, D., Gök, Y., Aktaş, A., Aygün, M., Taslimi, P., & Gülçin, İ. (2018). Novel benzylic substituted imidazolinium, tetrahydropyrimidinium and tetrahydrodiazepinium salts: Potent carbonic anhydrase and acetylcholinesterase inhibitors. ChemistrySelect, 3(27), 7976–7982. https://doi.org/https://doi.org/10.1002/slct.201801019
- Yiğit, B., Yiğit, M., Taslimi, P., Gök, Y., & Gülçin, İ. (2018). Schiff bases and their amines: Synthesis and discovery of carbonic anhydrase and acetylcholinesterase enzymes inhibitors. Archiv der Pharmazie, 351(9), 1800146. https://doi.org/https://doi.org/10.1002/ardp.201800146Ci
- Yin, Z., Zhang, W., Feng, F., Zhang, Y., & Kang, W. (2014). α-Glucosidase inhibitors isolated from medicinal plants. Food Science and Human Wellness, 3(3–4), 136–174. https://doi.org/https://doi.org/10.1016/j.fshw.2014.11.003
- Zengin, M., Genc, H., Taslimi, P., Kestane, A., Guclu, E., Ogutlu, A., Karabay, O., & Gulçin, İ. (2018). Novel thymol bearing oxypropanolamine derivatives as potent some metabolic enzyme inhibitors - Their antidiabetic, anticholinergic and antibacterial potentials. Bioorganic Chemistry, 81, 119–126. https://doi.org/https://doi.org/10.1016/j.bioorg.2018.08.003