1 Ocak 2021 Dergi makalesi Açık Erişim

Serdaroglu, Goncagul; Uludag, Nesimi; Ercag, Erol; Sugumar, Paramasivam; Rajkumar, Parthasarathi

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{
  "@context": "https://schema.org/", 
  "@id": 237086, 
  "@type": "ScholarlyArticle", 
  "creator": [
    {
      "@type": "Person", 
      "affiliation": "Sivas Cumhuriyet Univ, Fac Educ Math & Sci Edu, TR-58040 Sivas, Turkey", 
      "name": "Serdaroglu, Goncagul"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Namuk Kemal Univ, Dept Chem, TR-59030 Tekirdag, Turkey", 
      "name": "Uludag, Nesimi"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Namuk Kemal Univ, Dept Chem, TR-59030 Tekirdag, Turkey", 
      "name": "Ercag, Erol"
    }, 
    {
      "@type": "Person", 
      "name": "Sugumar, Paramasivam"
    }, 
    {
      "@type": "Person", 
      "affiliation": "King Nandhivarman Coll Arts & Sci, PG & Res Dept Phys, Thellar 604406, Tamil Nadu, India", 
      "name": "Rajkumar, Parthasarathi"
    }
  ], 
  "datePublished": "2021-01-01", 
  "description": "A various carbazole derivativeswere synthesized for the synthesis 2,3-Dihydro-1H-carbazol-4(9H)-one O-acetyl oxime (3), ethyl 2-(2,3,4,9-tetrahydrospiro[carbazole-1,2'-[1,3]dithiolane]-2-yl)acetate (5), 2- hydroxyethyl {2,3,4,9-tetrahydrospiro[1H-carbazole-1,2'[1,3]dithiolane-4-one]-2-yl}-acetamide (7). These products (3, 5, and 7) were characterized by the spectroscopic techniques (IR, H-1 NMR, C-13 NMR and elemental analysis). Then, the observed FT-IR and NMR peaks of the studied compounds were compared with the calculated values. The FMO analyses disclosed that the (5) would prefer intermolecular interactions more than intramolecular interactions because of its higher energy gap. NBO analyses displayed that the n ->Pi* and Pi ->Pi* interactionswere responsible for the lowering of the stabilization energy. Themolecular docking studies showed that (5) exhibited highest binding affinitywith the human glutathione reductase at binding site (-7.21 kcal/mol). Also, the antioxidant activities were investigated using the CUPRAC method, and TEAC coefficient implied that compound (3) have an antioxidant property. In addition, docking calculations of the compound (3), (5), and(7) were performed on bacterial tyrosinase enzyme and human glutathione reductase protein. (C) 2021 Elsevier B.V. All rights reserved.", 
  "headline": "Carbazole derivatives: Synthesis, spectroscopic characterization, antioxidant activity, molecular docking study, and the quantum chemical calculations", 
  "identifier": 237086, 
  "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", 
  "license": "http://www.opendefinition.org/licenses/cc-by", 
  "name": "Carbazole derivatives: Synthesis, spectroscopic characterization, antioxidant activity, molecular docking study, and the quantum chemical calculations", 
  "url": "https://aperta.ulakbim.gov.tr/record/237086"
}