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Synthesis of nitrogen-containing oleanolic acid derivatives as carbonic anhydrase and acetylcholinesterase inhibitors

Medicinal Chemistry Research, ISSN: 1554-8120, Vol: 32, Issue: 4, Page: 694-704
2023
  • 16
    Citations
  • 0
    Usage
  • 5
    Captures
  • 1
    Mentions
  • 0
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    16
  • Captures
    5
  • Mentions
    1
    • News Mentions
      1
      • 1

Most Recent News

Findings from Bezmialem Vakif University Has Provided New Data on Chemicals and Chemistry (Synthesis of Nitrogen-containing Oleanolic Acid Derivatives As Carbonic Anhydrase and Acetylcholinesterase Inhibitors)

2023 MAR 28 (NewsRx) -- By a News Reporter-Staff News Editor at Chemicals & Chemistry Daily Daily -- New research on Chemicals and Chemistry is

Article Description

In this study, a total of 13 compounds (5–17) were synthesized starting from oleanolic acid (OA), a natural triterpenoid. Five new compounds (10, 11, 12, 15 and 17), are the main targets of the study, which were synthesized for the first time in this work as oxime, imine and hydrazone derivatives of OA. Other compounds were previously obtained as natural or semi-synthetically. NMR and HRMS analyses were carried out to determine of structures of all the synthesized molecules. The inhibitory effects of the synthesized compounds on acetylcholinesterase (AChE), human carbonic anhydrase I (hCA I) and II (hCA II) were evaluated. Compounds 13 and 15 showed better inhibitory activity than the other compounds against both hCA I and hCA II isoenzymes, which are competing with AZA. In addition, compound 15 showed the strongest AChE inhibitory activity among all the tested compounds, with an IC value of 34.46 µM.

Bibliographic Details

Halil Şenol; Gurbet Çelik Turgut; Alaattin Şen; Rüya Sağlamtaş; Salih Tuncay; İlhami Gülçin; Gülaçtı Topçu

Springer Science and Business Media LLC

Pharmacology, Toxicology and Pharmaceutics; Chemistry

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