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  • Küçük Resim
    Öğe
    Determination of secondary metabolites of Cydonia oblonga (Quince) by LC-MS/MS method together with evaluation of its antioxidant and cholinergic potentials
    (ACG Publications, 2024) Dikici, Emrah; Altın, Sevgi; Alp, Cemalettin; Işık, Mesut; Köksal, Ekrem; Gülçin, İlhami
    In this study, quantification of secondary metabolites of Cydonia oblonga (Quince) leaves by LC-MS/MS and antioxidant, cholinergic and ?-Glycosidase activities were reported. LC-MS/MS analyses of the studied extract showed that the highest phenolic constituents of species were catechin (2024.9 ± 80.9 ?g/L), vanillic acid (1121.8 ± 39.3 ?g/L) and fumaric acid (486.7 ± 16.5 ?g/L). The ethanol extract of quince leaves inhibited the ?-glycosidase enzyme with an IC50: 0.6 ?g/mL value. In order to determine the anti-Alzheimer activity of the plant extract, inhibition studies were carried out on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes. The IC50 values of the plant extract were found to be 1.3 ?g/mL for AChE and 1.5 ?g/mL for BChE. In addition, free radical scavenging and metal reduction tests were performed to determine the antioxidant activity of the plant and the results were compared with Trolox. It was understood that the antioxidant potential of the plant was lower than Trolox. The results from biological abilities, molecular docking of catechin hydrate as abundant phenolic compounds in quince leaves extract to be an inhibitor candidate for AChE, BChE and ?-glycosidase.
  • Küçük Resim
    Öğe
    Sulfapyridine-like benzenesulfonamide derivatives as inhibitors of carbonic anhydrase isoenzymes I, II and VI
    (Taylor & Francis, 2012) Alp, Cemalettin; Özsoy, Şeyda; Alp, Nurdan Alcan; Erdem, Deryanur; Gültekin, Mehmet Serdar; Küfrevioğlu, Ömer İrfan; Şentürk, Murat; Supuran, Claudiu T.
    The inhibition of two human cytosolic carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I, II and human serum isozyme VI, with a series of tosylited aromatic amine derivatives was investigated. The K-I ranges of compounds 1-14 and acetazolamide against hCA I ranged between 1.130 and- 448.2 mu M, against hCA II between 0.103 and- 14.3 mu M, and against hCA VI ranged between 0.340 and- 42.39 mu M. Tosylited aromatic amine derivatives are thus interesting hCA I, II and VI inhibitors, and might be used as leads for generating enzyme inhibitors eventually targeting other isoforms which have not been assayed yet for their interactions with such agents.