Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensis

Eight cembrane-type diterpenoids, namely, (+)-(6R)-6-hydroxyisosarcophytoxide (1), (+)-(6R)-6-acetoxyisosarcophytoxide (2), (+)-17-hydroxyisosarcophytoxide (3), sarcomililatins A–D (4–7), and sarcomililatol (8), were isolated from the soft coral Sarcophyton mililatensis collected from Weizhou Island...

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Main Authors: Songwei Li, Fei Ye, Zhengdan Zhu, Hui Huang, Shuichun Mao, Yuewei Guo
Format: Article
Language:English
Published: Elsevier 2018-10-01
Series:Acta Pharmaceutica Sinica B
Online Access:http://www.sciencedirect.com/science/article/pii/S2211383518302119
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spelling doaj-7ed7bdc3acb04aa896d19ae5e4b08d602020-11-24T21:13:40ZengElsevierActa Pharmaceutica Sinica B2211-38352018-10-0186944955Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensisSongwei Li0Fei Ye1Zhengdan Zhu2Hui Huang3Shuichun Mao4Yuewei Guo5State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China; School of Pharmacy, Nanchang University, Nanchang 330006, ChinaState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, ChinaState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, ChinaKey Laboratory of Marine Bio-resources Sustainable Utilization, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, ChinaSchool of Pharmacy, Nanchang University, Nanchang 330006, China; Corresponding authors.State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China; Corresponding authors.Eight cembrane-type diterpenoids, namely, (+)-(6R)-6-hydroxyisosarcophytoxide (1), (+)-(6R)-6-acetoxyisosarcophytoxide (2), (+)-17-hydroxyisosarcophytoxide (3), sarcomililatins A–D (4–7), and sarcomililatol (8), were isolated from the soft coral Sarcophyton mililatensis collected from Weizhou Island, Guangxi Autonomous Region, together with 2 known related analogues, (+)-isosarcophytoxide (9) and (+)-isosarcophine (10). The structures of these compounds were elucidated by a combination of detailed spectroscopic analyses, chemical methods, and comparison with reported data. The absolute configuration of compound 1 was established by the modified Mosher׳s method, while the absolute configurations of compounds 4 and 5 were assigned by electronic circular dichroism (ECD) spectroscopy and that of compound 8 was established by time-dependent density functional theory electronic circular dichroism (TD-DFT ECD) calculation. In in vitro bioassays, compound 9 displayed significant cytotoxicity against the human cancer cell lines human promyelocytic leukemia cells (HL-60) and human lung adenocarcinoma cells (A-549) with IC50 values of 0.78±0.21 and 1.26±0.80 μmol/L, respectively. Compounds 4 and 9 also showed moderate inhibitory effects on the TNFα-induced Nuclear factor kappa B (NF-κB, a therapeutical target in cancer) activation, showing IC50 values of 35.23±12.42 and 22.52±4.44 μmol/L, respectively. Keywords: Soft coral, Sarcophyton, Sarcophyton mililatensis, Cembrane-type diterpe-noids, Modified Mosher׳s method, ECD calculation, Cytotoxicity, NF-κB inhibitory activityhttp://www.sciencedirect.com/science/article/pii/S2211383518302119
collection DOAJ
language English
format Article
sources DOAJ
author Songwei Li
Fei Ye
Zhengdan Zhu
Hui Huang
Shuichun Mao
Yuewei Guo
spellingShingle Songwei Li
Fei Ye
Zhengdan Zhu
Hui Huang
Shuichun Mao
Yuewei Guo
Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensis
Acta Pharmaceutica Sinica B
author_facet Songwei Li
Fei Ye
Zhengdan Zhu
Hui Huang
Shuichun Mao
Yuewei Guo
author_sort Songwei Li
title Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensis
title_short Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensis
title_full Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensis
title_fullStr Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensis
title_full_unstemmed Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensis
title_sort cembrane-type diterpenoids from the south china sea soft coral sarcophyton mililatensis
publisher Elsevier
series Acta Pharmaceutica Sinica B
issn 2211-3835
publishDate 2018-10-01
description Eight cembrane-type diterpenoids, namely, (+)-(6R)-6-hydroxyisosarcophytoxide (1), (+)-(6R)-6-acetoxyisosarcophytoxide (2), (+)-17-hydroxyisosarcophytoxide (3), sarcomililatins A–D (4–7), and sarcomililatol (8), were isolated from the soft coral Sarcophyton mililatensis collected from Weizhou Island, Guangxi Autonomous Region, together with 2 known related analogues, (+)-isosarcophytoxide (9) and (+)-isosarcophine (10). The structures of these compounds were elucidated by a combination of detailed spectroscopic analyses, chemical methods, and comparison with reported data. The absolute configuration of compound 1 was established by the modified Mosher׳s method, while the absolute configurations of compounds 4 and 5 were assigned by electronic circular dichroism (ECD) spectroscopy and that of compound 8 was established by time-dependent density functional theory electronic circular dichroism (TD-DFT ECD) calculation. In in vitro bioassays, compound 9 displayed significant cytotoxicity against the human cancer cell lines human promyelocytic leukemia cells (HL-60) and human lung adenocarcinoma cells (A-549) with IC50 values of 0.78±0.21 and 1.26±0.80 μmol/L, respectively. Compounds 4 and 9 also showed moderate inhibitory effects on the TNFα-induced Nuclear factor kappa B (NF-κB, a therapeutical target in cancer) activation, showing IC50 values of 35.23±12.42 and 22.52±4.44 μmol/L, respectively. Keywords: Soft coral, Sarcophyton, Sarcophyton mililatensis, Cembrane-type diterpe-noids, Modified Mosher׳s method, ECD calculation, Cytotoxicity, NF-κB inhibitory activity
url http://www.sciencedirect.com/science/article/pii/S2211383518302119
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