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Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study
Ceramicines are a series of limonoids which were isolated from the bark of Malaysian Chisocheton ceramicus (Meliaceae) and show various biological activities. Ceramicine B, in particular, has been reported to show a strong lipid droplet accumulation (LDA) inhibitory activity on a mouse pre-adipocyte...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Singapore
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459969/ https://www.ncbi.nlm.nih.gov/pubmed/28822030 http://dx.doi.org/10.1007/s11418-017-1109-2 |
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author | Nugroho, Alfarius Eko Hashimoto, Akiyo Wong, Chin-Piow Yokoe, Hiromasa Tsubuki, Masayoshi Kaneda, Toshio Hadi, A. Hamid A. Morita, Hiroshi |
author_facet | Nugroho, Alfarius Eko Hashimoto, Akiyo Wong, Chin-Piow Yokoe, Hiromasa Tsubuki, Masayoshi Kaneda, Toshio Hadi, A. Hamid A. Morita, Hiroshi |
author_sort | Nugroho, Alfarius Eko |
collection | PubMed |
description | Ceramicines are a series of limonoids which were isolated from the bark of Malaysian Chisocheton ceramicus (Meliaceae) and show various biological activities. Ceramicine B, in particular, has been reported to show a strong lipid droplet accumulation (LDA) inhibitory activity on a mouse pre-adipocyte cell line (MC3T3-G2/PA6). With the purpose of discovering compounds with stronger activity than ceramicine B, we further investigated the constituents of C. ceramicus. As a result, from the bark of C. ceramicus four new ceramicines (ceramicines M–P, 1–4) were isolated, and their structures were determined on the basis of NMR and mass spectroscopic analyses in combination with NMR chemical shift calculations. LDA inhibitory activity of 1–4 was evaluated. Compounds 1–3 showed LDA inhibitory activity, and 3 showed better selectivity than ceramicine B while showing activity at the same order of magnitude as ceramicine B. Since 3, which possess a carbonyl group at C-7, showed better selectivity than 5, which possess a 7α-OH group, while showing activity at the same order of magnitude as 5, we also investigated the effect of the substituent at C-7 by synthesizing several derivatives and evaluating their LDA inhibitory activity. Accordingly, we confirmed the importance of the presence of a 7α-OH group to the LDA inhibitory activity. |
format | Online Article Text |
id | pubmed-6459969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-64599692019-05-03 Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study Nugroho, Alfarius Eko Hashimoto, Akiyo Wong, Chin-Piow Yokoe, Hiromasa Tsubuki, Masayoshi Kaneda, Toshio Hadi, A. Hamid A. Morita, Hiroshi J Nat Med Original Paper Ceramicines are a series of limonoids which were isolated from the bark of Malaysian Chisocheton ceramicus (Meliaceae) and show various biological activities. Ceramicine B, in particular, has been reported to show a strong lipid droplet accumulation (LDA) inhibitory activity on a mouse pre-adipocyte cell line (MC3T3-G2/PA6). With the purpose of discovering compounds with stronger activity than ceramicine B, we further investigated the constituents of C. ceramicus. As a result, from the bark of C. ceramicus four new ceramicines (ceramicines M–P, 1–4) were isolated, and their structures were determined on the basis of NMR and mass spectroscopic analyses in combination with NMR chemical shift calculations. LDA inhibitory activity of 1–4 was evaluated. Compounds 1–3 showed LDA inhibitory activity, and 3 showed better selectivity than ceramicine B while showing activity at the same order of magnitude as ceramicine B. Since 3, which possess a carbonyl group at C-7, showed better selectivity than 5, which possess a 7α-OH group, while showing activity at the same order of magnitude as 5, we also investigated the effect of the substituent at C-7 by synthesizing several derivatives and evaluating their LDA inhibitory activity. Accordingly, we confirmed the importance of the presence of a 7α-OH group to the LDA inhibitory activity. Springer Singapore 2017-08-18 2018 /pmc/articles/PMC6459969/ /pubmed/28822030 http://dx.doi.org/10.1007/s11418-017-1109-2 Text en © The Author(s) 2017, corrected publication 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made. |
spellingShingle | Original Paper Nugroho, Alfarius Eko Hashimoto, Akiyo Wong, Chin-Piow Yokoe, Hiromasa Tsubuki, Masayoshi Kaneda, Toshio Hadi, A. Hamid A. Morita, Hiroshi Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study |
title | Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study |
title_full | Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study |
title_fullStr | Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study |
title_full_unstemmed | Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study |
title_short | Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study |
title_sort | ceramicines m–p from chisocheton ceramicus: isolation and structure–activity relationship study |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459969/ https://www.ncbi.nlm.nih.gov/pubmed/28822030 http://dx.doi.org/10.1007/s11418-017-1109-2 |
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