Chemical Investigation and Bioactivity Screening of Salvia cassia Extracts


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Halfon B., Cetin O., Kokdil G., TOPÇU G.

RECORDS OF NATURAL PRODUCTS, cilt.13, sa.2, ss.156-166, 2019 (SCI-Expanded, Scopus, TRDizin) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 13 Sayı: 2
  • Basım Tarihi: 2019
  • Doi Numarası: 10.25135/rnp.99.18.05.291
  • Dergi Adı: RECORDS OF NATURAL PRODUCTS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.156-166
  • Anahtar Kelimeler: Salvia cassia, antioxidant activity, anticholinesterase activity, fatty acid composition, beta-amyrin-fatty acid esters, flavonoids, ESSENTIAL OIL, ANTIOXIDANT ACTIVITY, TOTAL PHENOL, ANTICHOLINESTERASE, TRITERPENOIDS, DITERPENOIDS, CONSTITUENTS, RELEVANT, SPECTRA
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Bezmiâlem Vakıf Üniversitesi Adresli: Evet

Özet

In this study the antioxidant and anticholinesterase activities of the crude ethanol extract, as well as the dichloromethane and water extracts obtained from partitioning of the crude ethanol extract, of the plant Salvia cassia Samuelss ex. Rech. Fil, were determined. The extracts were screened for their total phenolic and flavonoid contents. The dichloromethane extract, which showed higher inhibition of lipid peroxidation, higher metal chelating capacity and also a higher flavonoid content than the other extracts was analyzed for its constituents. GC-MS analysis resulted in the identification of a total of 30 long chain hydrocarbons. A series of beta-amyrin fatty acid esters, a triterpene acid oleanolic acid, a diterpenoid manoyloxide, and two flavonoids apigenin 7, 4'-dimethyl ether and salvigenin were isolated by open column chromatography. Their structures were identified based on NMR and mass spectrometric techniques. The isolated compounds were also tested for their anticholinesterase activities. The triterpenoids as well as the water extract exhibited promising anticholinesterase activity.