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Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala

Three new steroidal carboxylic acids, paraminabic acids A–C (1–3) were isolated from a Formosan soft coral Paraminabea acronocephala. The structures of these compounds were established by extensive spectroscopic analysis and chemical methods. Application of the PGME method allowed the establishment...

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Autores principales: Chao, Chih-Hua, Wu, Yang-Chang, Wen, Zhi-Hong, Sheu, Jyh-Horng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564163/
https://www.ncbi.nlm.nih.gov/pubmed/23344155
http://dx.doi.org/10.3390/md11010136
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author Chao, Chih-Hua
Wu, Yang-Chang
Wen, Zhi-Hong
Sheu, Jyh-Horng
author_facet Chao, Chih-Hua
Wu, Yang-Chang
Wen, Zhi-Hong
Sheu, Jyh-Horng
author_sort Chao, Chih-Hua
collection PubMed
description Three new steroidal carboxylic acids, paraminabic acids A–C (1–3) were isolated from a Formosan soft coral Paraminabea acronocephala. The structures of these compounds were established by extensive spectroscopic analysis and chemical methods. Application of the PGME method allowed the establishment of the absolute configurations at C-25 and C-24 for 1 and 2, respectively. Compound 3 showed potent cytotoxicity toward Hep3B, MDA-MB-231, MCF-7, and A-549 cancer cell lines, with IC(50) values ranging from 2.05 to 2.83 μg/mL. Compounds 2 and 3 were found to inhibit the accumulation of the pro-inflammatory iNOS protein.
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spelling pubmed-35641632013-02-11 Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala Chao, Chih-Hua Wu, Yang-Chang Wen, Zhi-Hong Sheu, Jyh-Horng Mar Drugs Article Three new steroidal carboxylic acids, paraminabic acids A–C (1–3) were isolated from a Formosan soft coral Paraminabea acronocephala. The structures of these compounds were established by extensive spectroscopic analysis and chemical methods. Application of the PGME method allowed the establishment of the absolute configurations at C-25 and C-24 for 1 and 2, respectively. Compound 3 showed potent cytotoxicity toward Hep3B, MDA-MB-231, MCF-7, and A-549 cancer cell lines, with IC(50) values ranging from 2.05 to 2.83 μg/mL. Compounds 2 and 3 were found to inhibit the accumulation of the pro-inflammatory iNOS protein. MDPI 2013-01-11 /pmc/articles/PMC3564163/ /pubmed/23344155 http://dx.doi.org/10.3390/md11010136 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Chao, Chih-Hua
Wu, Yang-Chang
Wen, Zhi-Hong
Sheu, Jyh-Horng
Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala
title Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala
title_full Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala
title_fullStr Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala
title_full_unstemmed Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala
title_short Steroidal Carboxylic Acids from Soft Coral Paraminabea acronocephala
title_sort steroidal carboxylic acids from soft coral paraminabea acronocephala
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564163/
https://www.ncbi.nlm.nih.gov/pubmed/23344155
http://dx.doi.org/10.3390/md11010136
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