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Chemical Investigation of the Indonesian Tunicate Polycarpa aurata and Evaluation of the Effects Against Schistosoma mansoni of the Novel Alkaloids Polyaurines A and B.


ABSTRACT: A deep study of the metabolic content of the tunicate Polycarpa aurata, collected from Indonesian coast, afforded the isolation of two novel alkaloids, polyaurines A (1) and B (2), along with two new p-substituted benzoyl derivatives (3 and 4) and four known compounds (5-8). The structural elucidation of the new secondary metabolites was assigned by 1D, 2D NMR, and HRESIMS techniques. Computational studies resulted a useful tool to unambiguously determine in polyaurine B the presence of rarely found 1,2,4-thiadiazole ring. The effects of polyaurines A and B on mammalian cells growth and on the viability of different blood-dwelling Schistosoma mansoni (phylum: Platyhelminthes) stages, as well as egg production, were evaluated. Both compounds resulted not cytotoxic; interestingly some of the eggs produced by polyaurine A-treated adult pairs in vitro are smaller, deformed, and/or fragmented; therefore, polyaurine A could represent an interesting bioactive natural molecule to be further investigated.

SUBMITTER: Casertano M 

PROVIDER: S-EPMC6562961 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature

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Chemical Investigation of the Indonesian Tunicate <i>Polycarpa aurata</i> and Evaluation of the Effects Against <i>Schistosoma mansoni</i> of the Novel Alkaloids Polyaurines A and B.

Casertano Marcello M   Imperatore Concetta C   Luciano Paolo P   Aiello Anna A   Putra Masteria Yunovilsa MY   Gimmelli Roberto R   Ruberti Giovina G   Menna Marialuisa M  

Marine drugs 20190510 5


A deep study of the metabolic content of the tunicate <i>Polycarpa aurata</i>, collected from Indonesian coast, afforded the isolation of two novel alkaloids, polyaurines A (<b>1</b>) and B (<b>2</b>), along with two new <i>p</i>-substituted benzoyl derivatives (<b>3</b> and <b>4</b>) and four known compounds (<b>5</b>-<b>8</b>). The structural elucidation of the new secondary metabolites was assigned by 1D, 2D NMR, and HRESIMS techniques. Computational studies resulted a useful tool to unambigu  ...[more]

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