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Phenalenones from a Marine-Derived Fungus Penicillium sp.
Six new phenalenone derivatives (1–6), along with five known compounds (7–11) of the herqueinone class, were isolated from a marine-derived fungus Penicillium sp. The absolute configurations of these compounds were assigned based on chemical modifications and their specific rotations. 4-Hydroxyscler...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470642/ https://www.ncbi.nlm.nih.gov/pubmed/30889916 http://dx.doi.org/10.3390/md17030176 |
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author | Park, Sung Chul Julianti, Elin Ahn, Sungjin Kim, Donghwa Lee, Sang Kook Noh, Minsoo Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon |
author_facet | Park, Sung Chul Julianti, Elin Ahn, Sungjin Kim, Donghwa Lee, Sang Kook Noh, Minsoo Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon |
author_sort | Park, Sung Chul |
collection | PubMed |
description | Six new phenalenone derivatives (1–6), along with five known compounds (7–11) of the herqueinone class, were isolated from a marine-derived fungus Penicillium sp. The absolute configurations of these compounds were assigned based on chemical modifications and their specific rotations. 4-Hydroxysclerodin (6) and an acetone adduct of a triketone (7) exhibited moderate anti-angiogenetic and anti-inflammatory activities, respectively, while ent-peniciherqueinone (1) and isoherqueinone (9) exhibited moderate abilities to induce adipogenesis without cytotoxicity. |
format | Online Article Text |
id | pubmed-6470642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64706422019-04-27 Phenalenones from a Marine-Derived Fungus Penicillium sp. Park, Sung Chul Julianti, Elin Ahn, Sungjin Kim, Donghwa Lee, Sang Kook Noh, Minsoo Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon Mar Drugs Article Six new phenalenone derivatives (1–6), along with five known compounds (7–11) of the herqueinone class, were isolated from a marine-derived fungus Penicillium sp. The absolute configurations of these compounds were assigned based on chemical modifications and their specific rotations. 4-Hydroxysclerodin (6) and an acetone adduct of a triketone (7) exhibited moderate anti-angiogenetic and anti-inflammatory activities, respectively, while ent-peniciherqueinone (1) and isoherqueinone (9) exhibited moderate abilities to induce adipogenesis without cytotoxicity. MDPI 2019-03-18 /pmc/articles/PMC6470642/ /pubmed/30889916 http://dx.doi.org/10.3390/md17030176 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Park, Sung Chul Julianti, Elin Ahn, Sungjin Kim, Donghwa Lee, Sang Kook Noh, Minsoo Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon Phenalenones from a Marine-Derived Fungus Penicillium sp. |
title | Phenalenones from a Marine-Derived Fungus Penicillium sp. |
title_full | Phenalenones from a Marine-Derived Fungus Penicillium sp. |
title_fullStr | Phenalenones from a Marine-Derived Fungus Penicillium sp. |
title_full_unstemmed | Phenalenones from a Marine-Derived Fungus Penicillium sp. |
title_short | Phenalenones from a Marine-Derived Fungus Penicillium sp. |
title_sort | phenalenones from a marine-derived fungus penicillium sp. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470642/ https://www.ncbi.nlm.nih.gov/pubmed/30889916 http://dx.doi.org/10.3390/md17030176 |
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