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Antifungal and Ichthyotoxic Sesquiterpenoids from Santalum album Heartwood
In our continuing study on a survey of biologically active natural products from heartwood of Santalum album (Southwest Indian origin), we newly found potent fish toxic activity of an n-hexane soluble extract upon primary screening using killifish (medaka) and characterized α-santalol and β-santalol...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152050/ https://www.ncbi.nlm.nih.gov/pubmed/28698478 http://dx.doi.org/10.3390/molecules22071139 |
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author | Kim, Tae Hoon Hatano, Tsutomu Okamoto, Keinosuke Yoshida, Takashi Kanzaki, Hiroshi Arita, Michiko Ito, Hideyuki |
author_facet | Kim, Tae Hoon Hatano, Tsutomu Okamoto, Keinosuke Yoshida, Takashi Kanzaki, Hiroshi Arita, Michiko Ito, Hideyuki |
author_sort | Kim, Tae Hoon |
collection | PubMed |
description | In our continuing study on a survey of biologically active natural products from heartwood of Santalum album (Southwest Indian origin), we newly found potent fish toxic activity of an n-hexane soluble extract upon primary screening using killifish (medaka) and characterized α-santalol and β-santalol as the active components. The toxicity (median tolerance limit (TLm) after 24 h at 1.9 ppm) of α-santalol was comparable with that of a positive control, inulavosin (TLm after 24 h at 1.3 ppm). These fish toxic compounds including inulavosin were also found to show a significant antifungal effect against a dermatophytic fungus, Trichophyton rubrum. Based on a similarity of the morphological change of the immobilized Trichophyton hyphae in scanning electron micrographs between treatments with α-santalol and griseofulvin (used as the positive control), inhibitory effect of α-santalol on mitosis (the antifungal mechanism proposed for griseofulvin) was assessed using sea urchin embryos. As a result, α-santalol was revealed to be a potent antimitotic agent induced by interference with microtubule assembly. These data suggested that α-santalol or sandalwood oil would be promising to further practically investigate as therapeutic agent for cancers as well as fungal skin infections. |
format | Online Article Text |
id | pubmed-6152050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61520502018-11-13 Antifungal and Ichthyotoxic Sesquiterpenoids from Santalum album Heartwood Kim, Tae Hoon Hatano, Tsutomu Okamoto, Keinosuke Yoshida, Takashi Kanzaki, Hiroshi Arita, Michiko Ito, Hideyuki Molecules Article In our continuing study on a survey of biologically active natural products from heartwood of Santalum album (Southwest Indian origin), we newly found potent fish toxic activity of an n-hexane soluble extract upon primary screening using killifish (medaka) and characterized α-santalol and β-santalol as the active components. The toxicity (median tolerance limit (TLm) after 24 h at 1.9 ppm) of α-santalol was comparable with that of a positive control, inulavosin (TLm after 24 h at 1.3 ppm). These fish toxic compounds including inulavosin were also found to show a significant antifungal effect against a dermatophytic fungus, Trichophyton rubrum. Based on a similarity of the morphological change of the immobilized Trichophyton hyphae in scanning electron micrographs between treatments with α-santalol and griseofulvin (used as the positive control), inhibitory effect of α-santalol on mitosis (the antifungal mechanism proposed for griseofulvin) was assessed using sea urchin embryos. As a result, α-santalol was revealed to be a potent antimitotic agent induced by interference with microtubule assembly. These data suggested that α-santalol or sandalwood oil would be promising to further practically investigate as therapeutic agent for cancers as well as fungal skin infections. MDPI 2017-07-08 /pmc/articles/PMC6152050/ /pubmed/28698478 http://dx.doi.org/10.3390/molecules22071139 Text en © 2017 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 Kim, Tae Hoon Hatano, Tsutomu Okamoto, Keinosuke Yoshida, Takashi Kanzaki, Hiroshi Arita, Michiko Ito, Hideyuki Antifungal and Ichthyotoxic Sesquiterpenoids from Santalum album Heartwood |
title | Antifungal and Ichthyotoxic Sesquiterpenoids from Santalum album Heartwood |
title_full | Antifungal and Ichthyotoxic Sesquiterpenoids from Santalum album Heartwood |
title_fullStr | Antifungal and Ichthyotoxic Sesquiterpenoids from Santalum album Heartwood |
title_full_unstemmed | Antifungal and Ichthyotoxic Sesquiterpenoids from Santalum album Heartwood |
title_short | Antifungal and Ichthyotoxic Sesquiterpenoids from Santalum album Heartwood |
title_sort | antifungal and ichthyotoxic sesquiterpenoids from santalum album heartwood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152050/ https://www.ncbi.nlm.nih.gov/pubmed/28698478 http://dx.doi.org/10.3390/molecules22071139 |
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