Seven new lobane diterpenoids, namely, lobocatalens A-G (-), were isolated from the Xisha soft coral . Their structures, including their absolute configurations, were elucidated via spectroscopic analysis, comparison with the literature data, QM-MNR, and TDDFT-ECD calculations. Among them, lobocatalen A () is a new lobane diterpenoid with an unusual ether linkage between C-14 and C-18. In addition, compound showed moderate anti-inflammatory activity in the zebrafish models and cytotoxic activity against the K562 human cancer cell line.
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http://dx.doi.org/10.3390/md21040223 | DOI Listing |
Mar Drugs
March 2023
Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.
Seven new lobane diterpenoids, namely, lobocatalens A-G (-), were isolated from the Xisha soft coral . Their structures, including their absolute configurations, were elucidated via spectroscopic analysis, comparison with the literature data, QM-MNR, and TDDFT-ECD calculations. Among them, lobocatalen A () is a new lobane diterpenoid with an unusual ether linkage between C-14 and C-18.
View Article and Find Full Text PDFChin J Nat Med
November 2020
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China; Open Studio for Druggability Research of Marine Natural Products, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China; University of Chinese Academy of Sciences, Beijing 100049, China. Electronic address:
Lobane-type diterpenoids are not frequently discovered from marine soft corals. In this paper, three new lobane type diterpenes, 13-methoxyloba-8,10,15(16),17(18)-tetraene (1), 8,10,13(15)Z,16E-lobatetraene (2) and 19-hydroxy-lobatetraene (3), and a new natural compound, 17,18-epoxyloba-16-acetoxy-8,10,13(15)-trien (4), co-occurring with a known related diterpenoid, 18-methoxyloba-8,10,13(15),16(17)-tetraene (5), were isolated from the South China Sea soft coral Sinularia polydactyla. The structures of new compounds were determined by extensive spectroscopic analysis and by comparison with those reported in the literature.
View Article and Find Full Text PDFMar Drugs
April 2020
Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 804, Taiwan.
Further chemical investigation of the EtOAc extract of the soft coral resulted in the discovery of eleven new diterpenoids lobovarols F-P (-) of lobane- and prenyleudesmane-types, along with two known metabolites ( and ). The structures of the new metabolites were established by spectroscopic analyses, including 2D NMR experiments. The absolute configuration of was determined using Mosher's method.
View Article and Find Full Text PDFMar Drugs
September 2017
Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 804, Taiwan.
New lobane-based diterpenoids lobovarols A-D (-) and a prenyleudesmane-type diterpenoid lobovarol E () along with seven known related diterpenoids (-) were isolated from the ethyl acetate extract of a Taiwanese soft coral . Their structures were identified on the basis of multiple spectroscopic analyses and spectral comparison. The absolute configuration at C-16 of the known compound is reported herein for the first time.
View Article and Find Full Text PDFTwo new lobane diterpenoids, prenyl-α-elemenone (1) and ent-prenyl-β-elemene (2), along with ,a known compound, α-murrolene (3) were isolated from a population of Bomean soft coral Sinularia sp. The structures of these compounds were elucidated on the basis of spectroscopic, including 2D NMR, and HR-MS data. These compounds were tested for their cytotoxicity and antibacterial activities against antibiotic resistant clinical strains.
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