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Probing Anti-Proliferative 24-Homoscalaranes from a Sponge Lendenfeldiasp.


ABSTRACT: In the current study, an NMR spectroscopic pattern-based procedure for probing scalarane derivatives was performed and four new 24-homoscalaranes, lendenfeldaranes A-D (1- 4), along with three known compounds, 12?-acetoxy-22-hydroxy-24-methyl-24-oxoscalar-16-en- 25-al (5), felixin F (6), and 24-methyl-12,24,25-trioxoscalar-16-en-22-oic acid (7) were isolated from the sponge Lendenfeldia sp. The structures of scalaranes 1-7 were elucidated on the basis of spectroscopic analysis. Scalaranes 1-7 were further evaluated for their cytotoxicity toward a series of human cancer cell lines and the results suggested that 5 and 7 dominated in the anti- proliferative activity of the extract. The 18-aldehyde functionality was found to play a key role in their activity.

SUBMITTER: Peng BR 

PROVIDER: S-EPMC7074534 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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Probing Anti-Proliferative 24-Homoscalaranes from a Sponge <i>Lendenfeldia</i>sp.

Peng Bo-Rong BR   Lai Kuei-Hung KH   Chen You-Ying YY   Su Jui-Hsin JH   Huang Yusheng M YM   Chen Yu-Hsin YH   Lu Mei-Chin MC   Yu Steve Sheng-Fa SS   Duh Chang-Yih CY   Sung Ping-Jyun PJ  

Marine drugs 20200124 2


In the current study, an NMR spectroscopic pattern-based procedure for probing scalarane derivatives was performed and four new 24-homoscalaranes, lendenfeldaranes A-D (<b>1</b>- <b>4</b>), along with three known compounds, 12α-acetoxy-22-hydroxy-24-methyl-24-oxoscalar-16-en- 25-al (<b>5</b>), felixin F (<b>6</b>), and 24-methyl-12,24,25-trioxoscalar-16-en-22-oic acid (<b>7</b>) were isolated from the sponge <i>Lendenfeldia</i> sp. The structures of scalaranes <b>1</b>-<b>7</b> were elucidated o  ...[more]

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