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...

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Main Authors: Nugroho, Alfarius Eko, Hashimoto, Akiyo, Wong, Chin-Piow, Yokoe, Hiromasa, Tsubuki, Masayoshi, Kaneda, Toshio, A. Hadi, A. Hamid, Morita, Hiroshi
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Published: Springer Verlag (Germany) 2018
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Online Access:http://eprints.um.edu.my/21098/
https://doi.org/10.1007/s11418-017-1109-2
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spelling my.um.eprints.210982021-09-02T04:24:35Z http://eprints.um.edu.my/21098/ 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 A. Hadi, A. Hamid Morita, Hiroshi Q Science (General) QD Chemistry 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 Verlag (Germany) 2018 Article PeerReviewed Nugroho, Alfarius Eko and Hashimoto, Akiyo and Wong, Chin-Piow and Yokoe, Hiromasa and Tsubuki, Masayoshi and Kaneda, Toshio and A. Hadi, A. Hamid and Morita, Hiroshi (2018) Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study. Journal of Natural Medicines, 72 (1). pp. 64-72. ISSN 1340-3443 https://doi.org/10.1007/s11418-017-1109-2 doi:10.1007/s11418-017-1109-2
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic Q Science (General)
QD Chemistry
spellingShingle Q Science (General)
QD Chemistry
Nugroho, Alfarius Eko
Hashimoto, Akiyo
Wong, Chin-Piow
Yokoe, Hiromasa
Tsubuki, Masayoshi
Kaneda, Toshio
A. Hadi, A. Hamid
Morita, Hiroshi
Ceramicines M–P from Chisocheton ceramicus: isolation and structure–activity relationship study
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 Article
author Nugroho, Alfarius Eko
Hashimoto, Akiyo
Wong, Chin-Piow
Yokoe, Hiromasa
Tsubuki, Masayoshi
Kaneda, Toshio
A. Hadi, A. Hamid
Morita, Hiroshi
author_facet Nugroho, Alfarius Eko
Hashimoto, Akiyo
Wong, Chin-Piow
Yokoe, Hiromasa
Tsubuki, Masayoshi
Kaneda, Toshio
A. Hadi, A. Hamid
Morita, Hiroshi
author_sort Nugroho, Alfarius Eko
title 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_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_sort ceramicines m–p from chisocheton ceramicus: isolation and structure–activity relationship study
publisher Springer Verlag (Germany)
publishDate 2018
url http://eprints.um.edu.my/21098/
https://doi.org/10.1007/s11418-017-1109-2
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score 13.18916