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Terpenoids from the soft coral Sinularia sp. collected in Yongxing Island
Qin, G.-F.; Tang, X.-L.; Sun, Y.-T.; Luo, X.-C.; Zhang, J.; van Ofwegen, L.P.; Sung, P.-J.; Li, P.-L.; Li, G.-Q. (2018). Terpenoids from the soft coral Sinularia sp. collected in Yongxing Island. Mar. Drugs 16(4): 127 [1-15]. https://dx.doi.org/10.3390/md16040127
In: Marine Drugs. Molecular Diversity Preservation International (MDPI): Basel. ISSN 1660-3397; e-ISSN 1660-3397
Peer reviewed article  

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Trefwoord
    Sinularia May, 1898 [WoRMS]
Author keywords
    soft coral; Sinularia sp.; sesquiterpenoid; cembranoid; antimalarial; cytotoxicities; antiviral; targets inhibitory activities

Auteurs  Top 
  • Qin, G.-F.
  • Tang, X.-L.
  • Sun, Y.-T.
  • Luo, X.-C.
  • Zhang, J.
  • van Ofwegen, L.P.
  • Sung, P.-J.
  • Li, P.-L.
  • Li, G.-Q.

Abstract
    Three new sesquiterpenoids (sinuketal (1), sinulins A and B (2 and 3)) and two new cembranoids (sinulins C and D (4 and 5)), as well as eight known sesquiterpenoids (6–13) and eight known cembranoids (14–21), were isolated from the Xisha soft coral Sinularia sp. Their structures were elucidated by extensive spectroscopic analysis. Compound 1 possesses an unprecedented isopropyl-branched bicyclo [6.3.0] undecane carbon skeleton with unique endoperoxide moiety, and a plausible biosynthetic pathway of it was postulated. According to the reported biological properties of endoperoxide, the antimalarial, cytotoxic, antiviral, and target inhibitory activities of 1 were tested. Compound 1 showed mild in vitro antimalarial activity against Plasmodium falciparum 3D7, weak cytotoxic activities toward Jurkat, MDA-MB-231, and U2OS cell lines, inhibitory effects against influenza A viruses H1N1 and PR8, as well as mild target inhibitory activity against acetylcholinesterase. The other compounds were evaluated for cytotoxicities against HeLa, HCT-116, and A549 tumor cell lines and target inhibitory activities against protein tyrosine phosphatase 1B (PTP1B). Compound 20 exhibited cytotoxicities against HeLa and HCT-116, and compounds 5, 11, and 15 showed mild target inhibitory activities against PTP1B.

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