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For: Karimov A, Orujova A, Taslimi P, Sadeghian N, Mammadov B, Karaman HS, Farzaliyev V, Sujayev A, Tas R, Alwasel S, Gulçin İ. Novel functionally substituted esters based on sodium diethyldithiocarbamate derivatives: Synthesis, characterization, biological activity and molecular docking studies. Bioorg Chem 2020;99:103762. [PMID: 32224335 DOI: 10.1016/j.bioorg.2020.103762] [Cited by in Crossref: 18] [Cited by in F6Publishing: 28] [Article Influence: 9.0] [Reference Citation Analysis]
Number Citing Articles
1 Can Karanlık C, Karanlık G, Taslimi P, Erdoğmuş A. Improvement of photochemical and enzyme inhibition properties of new BODIPY compound by conjugation with cisplatin. Polyhedron 2022;225:116042. [DOI: 10.1016/j.poly.2022.116042] [Reference Citation Analysis]
2 Durmaz L, Kiziltas H, Guven L, Karagecili H, Alwasel S, Gulcin İ. Antioxidant, Antidiabetic, Anticholinergic, and Antiglaucoma Effects of Magnofluorine. Molecules 2022;27:5902. [PMID: 36144638 DOI: 10.3390/molecules27185902] [Reference Citation Analysis]
3 Topal M, Gulcin İ. Evaluation of the in vitro antioxidant, antidiabetic and anticholinergic properties of rosmarinic acid from rosemary (Rosmarinus officinalis L.). Biocatalysis and Agricultural Biotechnology 2022;43:102417. [DOI: 10.1016/j.bcab.2022.102417] [Reference Citation Analysis]
4 Bora RE, Bilgicli HG, Üç EM, Alagöz MA, Zengin M, Gulcin İ. Synthesis, characterization, Evaluation of Metabolic Enzyme Inhibitors and in silico Studies of Thymol Based 2-Amino Thiol and Sulfonic Acid Compounds. Chemico-Biological Interactions 2022. [DOI: 10.1016/j.cbi.2022.110134] [Reference Citation Analysis]
5 Madassery GP, M V, Panja S, P H, Dey R. Metal‐Free Synthesis of S‐Aryldithiocarbamates: Aryl C−S Bond Formation at Room Temperature†. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202202136] [Reference Citation Analysis]
6 Gulcin İ, Petrova OV, Taslimi P, Malysheva SF, Schmidt EY, Sobenina LN, Gusarova NK, Trofimov BA, Tuzun B, Farzaliyev VM, Alwasel S, Sujayev AR. Synthesis, Characterization, Molecular Docking, Acetylcholinesterase and α‐Glycosidase Inhibition Profiles of Nitrogen‐Based Novel Heterocyclic Compounds. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202200370] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
7 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] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 6.0] [Reference Citation Analysis]
8 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]
9 Mahmudov I, Demir Y, Sert Y, Abdullayev Y, Sujayev A, Alwasel SH, Gulcin I. Synthesis and inhibition profiles of N-benzyl- and N-allyl aniline derivatives against carbonic anhydrase and acetylcholinesterase – A molecular docking study. Arabian Journal of Chemistry 2022;15:103645. [DOI: 10.1016/j.arabjc.2021.103645] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 15.0] [Reference Citation Analysis]
10 Şenocak A, Taş NA, Taslimi P, Tüzün B, Aydin A, Karadağ A. Novel amino acid Schiff base Zn(II) complexes as new therapeutic approaches in diabetes and Alzheimer's disease: Synthesis, characterization, biological evaluation, and molecular docking studies. J Biochem Mol Toxicol 2021;:e22969. [PMID: 34812557 DOI: 10.1002/jbt.22969] [Reference Citation Analysis]
11 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] [Cited by in F6Publishing: 33] [Reference Citation Analysis]
12 Manzoor S, Gabr MT, Rasool B, Pal K, Hoda N. Dual targeting of acetylcholinesterase and tau aggregation: Design, synthesis and evaluation of multifunctional deoxyvasicinone analogues for Alzheimer's disease. Bioorg Chem 2021;116:105354. [PMID: 34562674 DOI: 10.1016/j.bioorg.2021.105354] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
13 Akıncıoğlu A, Göksu S, Naderi A, Akıncıoğlu H, Kılınç N, Gülçin İ. Cholinesterases, carbonic anhydrase inhibitory properties and in silico studies of novel substituted benzylamines derived from dihydrochalcones. Comput Biol Chem 2021;94:107565. [PMID: 34474201 DOI: 10.1016/j.compbiolchem.2021.107565] [Cited by in Crossref: 1] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
14 Günsel A, Taslimi P, Atmaca GY, Bilgiçli AT, Pişkin H, Ceylan Y, Erdoğmuş A, Yarasir MN, Gülçin İ. Novel potential metabolic enzymes inhibitor, photosensitizer and antibacterial agents based on water-soluble phthalocyanine bearing imidazole derivative. Journal of Molecular Structure 2021;1237:130402. [DOI: 10.1016/j.molstruc.2021.130402] [Cited by in Crossref: 3] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
15 Bal S, Demirci Ö, Şen B, Taşkın Tok T, Taslimi P, Aktaş A, Gök Y, Aygün M, Gülçin İ. Silver N ‐heterocyclic carbene complexes bearing fluorinated benzyl group: Synthesis, characterization, crystal structure, computational studies, and inhibitory properties against some metabolic enzymes. Appl Organomet Chem 2021;35. [DOI: 10.1002/aoc.6312] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
16 Mirzazadeh R, Asgari MS, Barzegari E, Pedrood K, Mohammadi-Khanaposhtani M, Sherafati M, Larijani B, Rastegar H, Rahmani H, Mahdavi M, Taslimi P, Üç EM, Gulçin İ. New quinoxalin-1,3,4-oxadiazole derivatives: Synthesis, characterization, in vitro biological evaluations, and molecular modeling studies. Arch Pharm (Weinheim) 2021;354:e2000471. [PMID: 33999440 DOI: 10.1002/ardp.202000471] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
17 Bingol Z, Kızıltaş H, Gören AC, Kose LP, Topal M, Durmaz L, Alwasel SH, Gulcin İ. Antidiabetic, anticholinergic and antioxidant activities of aerial parts of shaggy bindweed (Convulvulus betonicifolia Miller subsp.) - profiling of phenolic compounds by LC-HRMS. Heliyon 2021;7:e06986. [PMID: 34027185 DOI: 10.1016/j.heliyon.2021.e06986] [Cited by in Crossref: 2] [Cited by in F6Publishing: 18] [Article Influence: 2.0] [Reference Citation Analysis]
18 Kızıltaş H, Bingol Z, Gören AC, Kose LP, Durmaz L, Topal F, Alwasel SH, Gulcin İ. LC-HRMS Profiling and Antidiabetic, Anticholinergic, and Antioxidant Activities of Aerial Parts of Kınkor (Ferulago stellata). Molecules 2021;26:2469. [PMID: 33922645 DOI: 10.3390/molecules26092469] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 11.0] [Reference Citation Analysis]
19 Bal S, Demirci Ö, Şen B, Taslimi P, Aktaş A, Gök Y, Aygün M, Gülçin İ. PEPPSI type Pd(II)NHC complexes bearing chloro-/fluorobenzyl group: Synthesis, characterization, crystal structures, α-glycosidase and acetylcholinesterase inhibitory properties. Polyhedron 2021;198:115060. [DOI: 10.1016/j.poly.2021.115060] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
20 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: 17] [Article Influence: 11.0] [Reference Citation Analysis]
21 Wahyu Effendi SS, Tan SI, Ting WW, Ng IS. Enhanced recombinant Sulfurihydrogenibium yellowstonense carbonic anhydrase activity and thermostability by chaperone GroELS for carbon dioxide biomineralization. Chemosphere 2021;271:128461. [PMID: 33131750 DOI: 10.1016/j.chemosphere.2020.128461] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
22 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: 28] [Article Influence: 2.5] [Reference Citation Analysis]
23 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: 13] [Article Influence: 3.0] [Reference Citation Analysis]
24 Huseynova A, Kaya R, Taslimi P, Farzaliyev V, Mammadyarova X, Sujayev A, Tüzün B, Kocyigit UM, Alwasel S, Gulçin İ. Design, synthesis, characterization, biological evaluation, and molecular docking studies of novel 1,2-aminopropanthiols substituted derivatives as selective carbonic anhydrase, acetylcholinesterase and α-glycosidase enzymes inhibitors. Journal of Biomolecular Structure and Dynamics. [DOI: 10.1080/07391102.2020.1811772] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 4.5] [Reference Citation Analysis]
25 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: 40] [Article Influence: 10.0] [Reference Citation Analysis]
26 Demir Y, Taslimi P, Koçyiğit ÜM, Akkuş M, Özaslan MS, Duran HE, Budak Y, Tüzün B, Gürdere MB, Ceylan M, Taysi S, Gülçin İ, Beydemir Ş. Determination of the inhibition profiles of pyrazolyl-thiazole derivatives against aldose reductase and α-glycosidase and molecular docking studies. Arch Pharm (Weinheim) 2020;353:e2000118. [PMID: 32761859 DOI: 10.1002/ardp.202000118] [Cited by in Crossref: 15] [Cited by in F6Publishing: 29] [Article Influence: 7.5] [Reference Citation Analysis]
27 Alım Z, Köksal Z, Karaman M. Evaluation of some thiophene-based sulfonamides as potent inhibitors of carbonic anhydrase I and II isoenzymes isolated from human erythrocytes by kinetic and molecular modelling studies. Pharmacol Rep 2020;72:1738-48. [PMID: 32748253 DOI: 10.1007/s43440-020-00149-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
28 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: 28] [Article Influence: 6.0] [Reference Citation Analysis]
29 Taslimi P, Erden Y, Mamedov S, Zeynalova L, Ladokhina N, Tas R, Tuzun B, Sujayev A, Sadeghian N, Alwasel SH, Gulcin I. The biological activities, molecular docking studies, and anticancer effects of 1-arylsuphonylpyrazole derivatives. J Biomol Struct Dyn 2021;39:3336-46. [PMID: 32364008 DOI: 10.1080/07391102.2020.1763838] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 3.5] [Reference Citation Analysis]