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New sesquiterpenes from Asteriscus graveolens.
Achoub, Hanane; Mencherini, Teresa; Esposito, Tiziana; Luca, Rastrelli; Aquino, Rita; Gazzerro, Patrizia; Zaiter, Lahcene; Benayache, Fadila; Benayache, Samir.
Affiliation
  • Achoub H; Unité de recherche Valorisation des Ressources Naturelles, Molécules Bioactives et Analyses Physicochimiques et Biologiques, Université Frères Mentouri, Constantine, Algeria.
  • Mencherini T; Department of Pharmacy, University of Salerno, Fisciano, Salerno, Italy.
  • Esposito T; Department of Pharmacy, University of Salerno, Fisciano, Salerno, Italy.
  • Luca R; Department of Pharmacy, University of Salerno, Fisciano, Salerno, Italy.
  • Aquino R; Department of Pharmacy, University of Salerno, Fisciano, Salerno, Italy.
  • Gazzerro P; Department of Pharmacy, University of Salerno, Fisciano, Salerno, Italy.
  • Zaiter L; Unité de recherche Valorisation des Ressources Naturelles, Molécules Bioactives et Analyses Physicochimiques et Biologiques, Université Frères Mentouri, Constantine, Algeria.
  • Benayache F; Unité de recherche Valorisation des Ressources Naturelles, Molécules Bioactives et Analyses Physicochimiques et Biologiques, Université Frères Mentouri, Constantine, Algeria.
  • Benayache S; Unité de recherche Valorisation des Ressources Naturelles, Molécules Bioactives et Analyses Physicochimiques et Biologiques, Université Frères Mentouri, Constantine, Algeria.
Nat Prod Res ; 35(13): 2190-2198, 2021 Jul.
Article in En | MEDLINE | ID: mdl-31542956
ABSTRACT
Asteriscus graveolens (Forsk) Less. is a Saharan medicinal plant of Asteraceae family. A new acyclic sesquiterpene [7,12-dihydroxy-6,7-dihydro-5,(6) E-dehydronerolidol (3)] and sesquiterpene germacranolide lactone derivatives [9ß-hydroxy-11ß,13-dihydroparthenolide-9-O-ß-D-glucopyranoside (7) and 9α-hydroxy-11ß,13-dihydroparthenolide-9-O-ß-D-glucopyranoside (8)] along with eight known compounds were isolated from polar extracts of aerial parts. Their structures were established by the analysis of 1 D- 2 D-NMR and high-resolution mass spectrometry data. A. graveolens extracts and compounds showed a significant (P < 0.05) and concentration dependent inhibitory effect on the growth of Human Colon Carcinoma (HCT116) and Human Colorectal Adenocarcinoma (DLD1) cells with IC50 in a concentration range from 89.4 to 296.0 µg/mL for extracts and from 32.6 to 728.1 µg/mL for compounds. No cytotoxic effects was evidenced in normal Primary Human Dermal Fibroblast (HDFa) up to 0.050 mg/mL for extracts and 1.0 mg/mL for pure compounds.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sesquiterpenes / Asteraceae Limits: Humans Language: En Journal: Nat Prod Res Year: 2021 Document type: Article Affiliation country: Argelia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sesquiterpenes / Asteraceae Limits: Humans Language: En Journal: Nat Prod Res Year: 2021 Document type: Article Affiliation country: Argelia