Anti-Inflammatory Lobane and Prenyleudesmane Diterpenoids from the Soft Coral Lobophytum varium

被引:12
作者
Ahmed, Atallah F. [1 ,2 ,3 ]
Teng, Wan-Ting [1 ]
Huang, Chiung-Yao [1 ]
Dai, Chang-Feng [4 ]
Hwang, Tsong-Long [5 ,6 ,7 ,8 ]
Sheu, Jyh-Horng [1 ,9 ,10 ,11 ,12 ]
机构
[1] Natl Sun Yat Sen Univ, Dept Marine Biotechnol & Resources, Kaohsiung 804, Taiwan
[2] King Saud Univ, Dept Pharmacognosy, Coll Pharm, Riyadh 11451, Saudi Arabia
[3] Mansoura Univ, Dept Pharmacognosy, Fac Pharm, Mansoura 35516, Egypt
[4] Natl Taiwan Univ, Inst Oceanog, Taipei 112, Taiwan
[5] Chang Gung Univ, Grad Inst Nat Prod, Coll Med, Taoyuan 333, Taiwan
[6] Chang Gung Univ Sci & Technol, Res Ctr Chinese Herbal Med, Res Ctr Food & Cosmet Safety, Coll Human Ecol, Taoyuan 333, Taiwan
[7] Chang Gung Univ Sci & Technol, Grad Inst Hlth Ind Technol, Coll Human Ecol, Taoyuan 333, Taiwan
[8] Chang Gung Mem Hosp, Dept Anesthesiol, Taoyuan 333, Taiwan
[9] Kaohsiung Med Univ, Inst Nat Prod, Kaohsiung 807, Taiwan
[10] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung 404, Taiwan
[11] Natl Sun Yat Sen Univ, Frontier Ctr Ocean Sci & Technol, Kaohsiung 804, Taiwan
[12] Natl Sun Yat Sen Univ, Doctoral Degree Program Marine Biotechnol, Kaohsiung 804, Taiwan
关键词
soft coral; Lobophytum varium; lobane; prenyleudesmane; anti-inflammatory activity; MARINE NATURAL-PRODUCTS; INHIBITS SUPEROXIDE-PRODUCTION; HUMAN NEUTROPHILS; ABSOLUTE-CONFIGURATIONS; ELASTASE RELEASE; CEMBRANOIDS; PAUCIFLORUM; DERIVATIVES; FUSCOL; BISCEMBRANOIDS;
D O I
10.3390/md15100300
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
New lobane-based diterpenoids lobovarols A-D (1-4) and a prenyleudesmane-type diterpenoid lobovarol E (5) along with seven known related diterpenoids (6-12) were isolated from the ethyl acetate extract of a Taiwanese soft coral Lobophytum varium. Their structures were identified on the basis of multiple spectroscopic analyses and spectral comparison. The absolute configuration at C-16 of the known compound 11 is reported herein for the first time. The anti-inflammatory activities of compounds 1-12 were assessed by measuring their inhibitory effect on N-formyl-methionyl-leucyl-phenyl-alanine/cytochalasin B (fMLP/CB)-induced superoxide anion generation and elastase release in human neutrophils. Metabolites 2, 5, and 11 were found to show moderate inhibitory activity on the generation of superoxide anion, while compounds 5, 8, 11, and 12 could effectively suppress elastase release in fMLP/CB-stimulated human neutrophil cells at 10 M. All of the isolated diterpenoids did not exhibit cytotoxic activity (IC50 > 50 M) towards a limited panel of cancer cell lines.
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页数:14
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