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Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds
Three new multiflorane-type triterpene esters, i.e. 7α-hydroxymultiflor-8-ene-3α,29-diol 3-acetate-29-benzoate (1), 7α-methoxymultiflor-8-ene-3α,29-diol 3,29-dibenzoate (2), and 7β-methoxymultiflor-8-ene-3α,29-diol 3,29-dibenzoate (3), were isolated from seeds of Cucurbita maxima, along with the kno...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271469/ https://www.ncbi.nlm.nih.gov/pubmed/24743937 http://dx.doi.org/10.3390/molecules19044802 |
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author | Kikuchi, Takashi Ueda, Shinsuke Kanazawa, Jokaku Naoe, Hiroki Yamada, Takeshi Tanaka, Reiko |
author_facet | Kikuchi, Takashi Ueda, Shinsuke Kanazawa, Jokaku Naoe, Hiroki Yamada, Takeshi Tanaka, Reiko |
author_sort | Kikuchi, Takashi |
collection | PubMed |
description | Three new multiflorane-type triterpene esters, i.e. 7α-hydroxymultiflor-8-ene-3α,29-diol 3-acetate-29-benzoate (1), 7α-methoxymultiflor-8-ene-3α,29-diol 3,29-dibenzoate (2), and 7β-methoxymultiflor-8-ene-3α,29-diol 3,29-dibenzoate (3), were isolated from seeds of Cucurbita maxima, along with the known compound, multiflora-7,9(11)-diene-3α,29-diol 3,29-dibenzoate (4). Compound 1 exhibited melanogenesis inhibitory activities comparable with those of arbutin. In cytotoxicity assays, compounds 1 and 3 exhibited weak cytotoxicity, with IC(50) values of 34.5–93.7 μM against HL-60 and P388 cells. |
format | Online Article Text |
id | pubmed-6271469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62714692019-01-02 Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds Kikuchi, Takashi Ueda, Shinsuke Kanazawa, Jokaku Naoe, Hiroki Yamada, Takeshi Tanaka, Reiko Molecules Article Three new multiflorane-type triterpene esters, i.e. 7α-hydroxymultiflor-8-ene-3α,29-diol 3-acetate-29-benzoate (1), 7α-methoxymultiflor-8-ene-3α,29-diol 3,29-dibenzoate (2), and 7β-methoxymultiflor-8-ene-3α,29-diol 3,29-dibenzoate (3), were isolated from seeds of Cucurbita maxima, along with the known compound, multiflora-7,9(11)-diene-3α,29-diol 3,29-dibenzoate (4). Compound 1 exhibited melanogenesis inhibitory activities comparable with those of arbutin. In cytotoxicity assays, compounds 1 and 3 exhibited weak cytotoxicity, with IC(50) values of 34.5–93.7 μM against HL-60 and P388 cells. MDPI 2014-04-16 /pmc/articles/PMC6271469/ /pubmed/24743937 http://dx.doi.org/10.3390/molecules19044802 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Kikuchi, Takashi Ueda, Shinsuke Kanazawa, Jokaku Naoe, Hiroki Yamada, Takeshi Tanaka, Reiko Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds |
title | Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds |
title_full | Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds |
title_fullStr | Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds |
title_full_unstemmed | Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds |
title_short | Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds |
title_sort | three new triterpene esters from pumpkin (cucurbita maxima) seeds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271469/ https://www.ncbi.nlm.nih.gov/pubmed/24743937 http://dx.doi.org/10.3390/molecules19044802 |
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