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Novel Caryophyllane-Related Sesquiterpenoids with Anti-Inflammatory Activity from Rumphella antipathes (Linnaeus, 1758).


ABSTRACT: Two previously undescribed caryophyllane-related sesquiterpenoids, antipacids A (1) and B (2), with a novel bicyclo[5.2.0] core skeleton, and known compound clovane-2?,9?-diol (3), along with rumphellolide L (4), an esterified product of 1 and 3, were isolated from the organic extract of octocoral Rumphella antipathes. Their structures, including the absolute configurations were elucidated by spectroscopic and chemical experiments. In vivo anti-inflammatory activity analysis indicated that antipacid B (2) inhibited the generation of superoxide anions and the release of elastase by human neutrophils, with IC50 values of 11.22 and 23.53 ?M, respectively, while rumphellolide L (4) suppressed the release of elastase with an IC50 value of 7.63 ?M.

SUBMITTER: Chang YC 

PROVIDER: S-EPMC7694975 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

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Novel Caryophyllane-Related Sesquiterpenoids with Anti-Inflammatory Activity from <i>Rumphella antipathes</i> (Linnaeus, 1758).

Chang Yu-Chia YC   Chiang Chih-Chao CC   Chang Yuan-Shiun YS   Chen Jih-Jung JJ   Wang Wei-Hsien WH   Fang Lee-Shing LS   Chung Hsu-Ming HM   Hwang Tsong-Long TL   Sung Ping-Jyun PJ  

Marine drugs 20201106 11


Two previously undescribed caryophyllane-related sesquiterpenoids, antipacids A (<b>1</b>) and B (<b>2</b>), with a novel bicyclo[5.2.0] core skeleton, and known compound clovane-2β,9α-diol (<b>3</b>), along with rumphellolide L (<b>4</b>), an esterified product of <b>1</b> and <b>3</b>, were isolated from the organic extract of octocoral <i>Rumphella antipathes</i>. Their structures, including the absolute configurations were elucidated by spectroscopic and chemical experiments. In vivo anti-in  ...[more]

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