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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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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. |
format | Online Article Text |
id | pubmed-3564163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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