MS/MS Molecular Networking Unveils the Chemical Diversity of Biscembranoid Derivatives, Neutrophilic Inflammatory Mediators from the Cultured Soft Coral Sarcophyton trocheliophorum

Biscembranoids are the distinctive tetraterpenoids owing a 14/6/14 membered tricyclic scaffold that have been mainly discovered in the soft corals, especially the genera , and . Recent findings have demonstrated the great anti-inflammatory potential of biscembranoid analogues in human neutrophils, m...

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Veröffentlicht in:International journal of molecular sciences 2022-12, Vol.23 (24), p.15464
Hauptverfasser: Nguyen, Ngoc Bao An, Chen, Lo-Yun, Chen, Po-Jen, El-Shazly, Mohamed, Hwang, Tsong-Long, Su, Jui-Hsin, Su, Chun-Han, Yen, Pei-Tzu, Peng, Bo-Rong, Lai, Kuei-Hung
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Sprache:eng
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Zusammenfassung:Biscembranoids are the distinctive tetraterpenoids owing a 14/6/14 membered tricyclic scaffold that have been mainly discovered in the soft corals, especially the genera , and . Recent findings have demonstrated the great anti-inflammatory potential of biscembranoid analogues in human neutrophils, motivating more chemical and biological explorations targeting these marine-derived natural products. In the current study, the chemical diversity of biscembranoids derived from the cultured-type von Marenzeller was illustrated through MS/MS molecular networking (MN) profiling approach. Based on the MN patterns, the prioritization of unknown biscembranoid derivatives was putatively analyzed. As a result, the biscembrane targeting isolation afforded two new metabolites, sarcotrochelides A ( ) and B ( ), along with six known analogues ( - ). Their structures and relative configurations were determined by spectroscopic methods. In vitro neutrophil inflammatory inhibition was further investigated for all isolates based on reduced superoxide anion (O ) generation detections. Compounds - showed significant dose-dependently inhibitory effects, suggesting the cruciality of 6,7-dihydrooxepin-2(5H)-one moiety and saturated γ-lactone ring in their reactive oxygen species (ROS)-dependent anti-inflammatory properties.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms232415464