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Journal Abstract Search

255 related items for PubMed ID: 30074266

  • 1. Synthesis of novel sulfamides incorporating phenethylamines and determination of their inhibition profiles against some metabolic enzymes.
    Aksu K, Akıncıoğlu H, Akıncıoğlu A, Göksu S, Tümer F, Gülçin İ.
    Arch Pharm (Weinheim); 2018 Sep; 351(9):e1800150. PubMed ID: 30074266
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  • 2. The synthesis of novel sulfamides derived from β-benzylphenethylamines as acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase enzymes inhibitors.
    Akıncıoğlu A, Kocaman E, Akıncıoğlu H, Salmas RE, Durdagi S, Gülçin İ, Supuran CT, Göksu S.
    Bioorg Chem; 2017 Oct; 74():238-250. PubMed ID: 28866249
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  • 4. Synthesis of diaryl ethers with acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase inhibitory actions.
    Özbey F, Taslimi P, Gülçin İ, Maraş A, Göksu S, Supuran CT.
    J Enzyme Inhib Med Chem; 2016 Oct; 31(sup2):79-85. PubMed ID: 27241224
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  • 6. Schiff bases and their amines: Synthesis and discovery of carbonic anhydrase and acetylcholinesterase enzymes inhibitors.
    Yiğit B, Yiğit M, Taslimi P, Gök Y, Gülçin İ.
    Arch Pharm (Weinheim); 2018 Sep; 351(9):e1800146. PubMed ID: 30033646
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  • 7. Inhibition Profiles of Some Symmetric Sulfamides Derived from Phenethylamines on Human Carbonic Anhydrase I, and II Isoenzymes.
    Topal F, Aksu K, Gulcin I, Tümer F, Goksu S.
    Chem Biodivers; 2021 Oct; 18(10):e2100422. PubMed ID: 34387019
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  • 8. Synthesis of 4,5-disubstituted-2-thioxo-1,2,3,4-tetrahydropyrimidines and investigation of their acetylcholinesterase, butyrylcholinesterase, carbonic anhydrase I/II inhibitory and antioxidant activities.
    Garibov E, Taslimi P, Sujayev A, Bingol Z, Çetinkaya S, Gulçin İ, Beydemir S, Farzaliyev V, Alwasel SH, Supuran CT.
    J Enzyme Inhib Med Chem; 2016 Oct; 31(sup3):1-9. PubMed ID: 27329935
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  • 13. Carbonic anhydrase inhibitory properties of novel benzylsulfamides using molecular modeling and experimental studies.
    Göksu S, Naderi A, Akbaba Y, Kalın P, Akıncıoğlu A, Gülçin İ, Durdagi S, Salmas RE.
    Bioorg Chem; 2014 Oct; 56():75-82. PubMed ID: 25159522
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  • 14. 1H-indazole molecules reduced the activity of human erythrocytes carbonic anhydrase I and II isoenzymes.
    Alim Z.
    J Biochem Mol Toxicol; 2018 Sep; 32(9):e22194. PubMed ID: 29984869
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  • 16. Cholinesterases, carbonic anhydrase inhibitory properties and in silico studies of novel substituted benzylamines derived from dihydrochalcones.
    Akıncıoğlu A, Göksu S, Naderi A, Akıncıoğlu H, Kılınç N, Gülçin İ.
    Comput Biol Chem; 2021 Oct; 94():107565. PubMed ID: 34474201
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  • 17. Synthesis, characterization, and SAR of arylated indenoquinoline-based cholinesterase and carbonic anhydrase inhibitors.
    Ekiz M, Tutar A, Ökten S, Bütün B, Koçyiğit ÜM, Taslimi P, Topçu G.
    Arch Pharm (Weinheim); 2018 Sep; 351(9):e1800167. PubMed ID: 30079554
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  • 18. 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.
    Lolak N, Akocak S, Türkeş C, Taslimi P, Işık M, Beydemir Ş, Gülçin İ, Durgun M.
    Bioorg Chem; 2020 Jul; 100():103897. PubMed ID: 32413628
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  • 20. Synthesis and evaluation of N-heteroarylsubstituted triazolosulfonamides as carbonic anhydrase inhibitors.
    Balci A, Arslan M, Nixha AR, Bilen C, Ergun A, Gençer N.
    J Enzyme Inhib Med Chem; 2015 Jun; 30(3):377-82. PubMed ID: 25068730
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