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Erschienen in: Journal of Natural Medicines 2/2018

20.02.2018 | Original Paper

Agarotetrol: a source compound for low molecular weight aromatic compounds from agarwood heating

verfasst von: Sakura Takamatsu, Michiho Ito

Erschienen in: Journal of Natural Medicines | Ausgabe 2/2018

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Abstract

Agarwood is known to generate a distinct fragrance upon heating and is used as both a medicine and a fragrant wood. Low molecular weight aromatic compounds (LACs) such as benzylacetone are emitted from agarwood on heating and have a sedative effect on mice. These are detected exclusively in the headspace vapor of heated agarwood and are absent in the wood itself; hence, some compounds in agarwood are thought to be converted to LACs by the process of heating. In this study, different fractions obtained from agarwood were analyzed to reveal the source compounds of LACs. Some LACs detected in the resinous agarwood were absent from the non-resinous parts and confirmed as characteristic of the resinous parts. The essential oil and hydrosol of agarwood obtained by distillation were analyzed by gas chromatography–mass spectrometry (GC–MS). Sesquiterpenes were detected in the essential oil, and sesquiterpenes and a variety of LACs were detected in the hydrosol. A hot water extract of agarwood remaining in the distillation flask after distillation was analyzed by high-performance liquid chromatography (HPLC), and agarotetrol was found to be the main compound. Purified agarotetrol was heated in a glass vial and its headspace vapor was analyzed by solid-phase microextraction GC–MS. Benzylacetone and other LACs were detected. These results indicate that agarotetrol, a chromone derivative, contributes to the fragrance of agarwood through the generation of LACs upon heating.
Literatur
1.
Zurück zum Zitat ANNUAL REPORT OF THE SECRETARIAT 2004, Convention on International Trade in Endangered Species of Wild Fauna and Flora, Appendices II ANNUAL REPORT OF THE SECRETARIAT 2004, Convention on International Trade in Endangered Species of Wild Fauna and Flora, Appendices II
2.
Zurück zum Zitat Takemoto H, Ito M, Shiraki T, Yagura T, Honda G (2008) Sedative effects of vapor inhalation of agarwood oil and spikenard extract and identification of their active compounds. J Nat Med 62:41–46CrossRef Takemoto H, Ito M, Shiraki T, Yagura T, Honda G (2008) Sedative effects of vapor inhalation of agarwood oil and spikenard extract and identification of their active compounds. J Nat Med 62:41–46CrossRef
3.
Zurück zum Zitat Kishida K, Ito M (2009) Components of agarwood oils and their effects on spontaneous motor activity of mice. Shoyakugaku Zasshi 63(2):39–45 Kishida K, Ito M (2009) Components of agarwood oils and their effects on spontaneous motor activity of mice. Shoyakugaku Zasshi 63(2):39–45
4.
Zurück zum Zitat Neaf R (2011) The volatile and semi-volatile constituents of agarwood, the infected heartwood of Aquilaria species: a review. Flavor Fragr J 26:73–89CrossRef Neaf R (2011) The volatile and semi-volatile constituents of agarwood, the infected heartwood of Aquilaria species: a review. Flavor Fragr J 26:73–89CrossRef
5.
Zurück zum Zitat Ishihara M, Tsuneya T (1993) Compounds of the agarwood smoke on heating. J Essent Oil Res 5:419–423CrossRef Ishihara M, Tsuneya T (1993) Compounds of the agarwood smoke on heating. J Essent Oil Res 5:419–423CrossRef
6.
Zurück zum Zitat Miyoshi T, Ito M, Kitayama T, Isomari S, Yamashita F (2013) Sedative effects of inhaled benzylacetone and structual features contributing to its activity. Biol Pharm Bull 36(9):1474–1481CrossRef Miyoshi T, Ito M, Kitayama T, Isomari S, Yamashita F (2013) Sedative effects of inhaled benzylacetone and structual features contributing to its activity. Biol Pharm Bull 36(9):1474–1481CrossRef
7.
Zurück zum Zitat Takakuwa T, Shimizu M, Kubo K, Takeuchi F, Nishio S (1977) Koseikagakukenkyuhokoku, Showa 52 nendo, 92 Takakuwa T, Shimizu M, Kubo K, Takeuchi F, Nishio S (1977) Koseikagakukenkyuhokoku, Showa 52 nendo, 92
8.
Zurück zum Zitat Hashimoto K, Nakahara S, Inoue T, Shimada Y, Takahashi M (1985) A new chromone from agarwood and pyrolysis products of chromone derivatives. Chem Pharm Bull 33(11):5088–5091CrossRef Hashimoto K, Nakahara S, Inoue T, Shimada Y, Takahashi M (1985) A new chromone from agarwood and pyrolysis products of chromone derivatives. Chem Pharm Bull 33(11):5088–5091CrossRef
9.
Zurück zum Zitat Zambonin CG, Balest L, De Benedetto GE, Palmisano F (2005) Solid-phase microextraction-gas chromatography mass spectrometry and multivariate analysis for the characterization of roasted coffees. Talanta 66:261–265CrossRef Zambonin CG, Balest L, De Benedetto GE, Palmisano F (2005) Solid-phase microextraction-gas chromatography mass spectrometry and multivariate analysis for the characterization of roasted coffees. Talanta 66:261–265CrossRef
10.
Zurück zum Zitat Łucejko JJ, Modugno F, Ribechini E, Del Río JC (2009) Characterisation of archaeological waterlogged wood by pyrolytic and mass spectrometric techniques. Anal Chim Acta 654:26–34CrossRef Łucejko JJ, Modugno F, Ribechini E, Del Río JC (2009) Characterisation of archaeological waterlogged wood by pyrolytic and mass spectrometric techniques. Anal Chim Acta 654:26–34CrossRef
11.
Zurück zum Zitat Shimada Y, Konishi T, Kiyosawa S, Nishi M, Miyahara K, Kawasaki T (1986) Studies on the agarwood (Jinko). IV. Structures of 2-(2-phenylethyl)chromone derivatives, agarotetrol and isoagarotetrol. Chem Pharm Bull 34(7):2766–2773CrossRef Shimada Y, Konishi T, Kiyosawa S, Nishi M, Miyahara K, Kawasaki T (1986) Studies on the agarwood (Jinko). IV. Structures of 2-(2-phenylethyl)chromone derivatives, agarotetrol and isoagarotetrol. Chem Pharm Bull 34(7):2766–2773CrossRef
12.
Zurück zum Zitat Yoshii E, Koizumi T, Oribe T (1978) The structure of agarotetrol, a novel highly oxygenated chromone from agarwood (Jinko). Tetrahedron Lett 41:3921–3924CrossRef Yoshii E, Koizumi T, Oribe T (1978) The structure of agarotetrol, a novel highly oxygenated chromone from agarwood (Jinko). Tetrahedron Lett 41:3921–3924CrossRef
13.
Zurück zum Zitat Konishi T, Okutani Y, Iwagoe K, Kiyosawa S, Shimada Y (1989) Studies of the agarwood “Jinko” (IX)1) quantitative analysis of 2-(2-phenylethyl)chromone derivatives (Supplement). Shoyakugaku Zasshi 43(1):1–6 Konishi T, Okutani Y, Iwagoe K, Kiyosawa S, Shimada Y (1989) Studies of the agarwood “Jinko” (IX)1) quantitative analysis of 2-(2-phenylethyl)chromone derivatives (Supplement). Shoyakugaku Zasshi 43(1):1–6
14.
Zurück zum Zitat Li J, Chen D, Jiang Y, Zhang Q, Zhang L, Tu PF (2013) Identification and quantification of 5,6,7,8-tetrahydro-2-(2-phenylethyl)chromones in Chinese eaglewood by HPLC with diode array detection and MS. J Sep Sci 36:3733–3740CrossRef Li J, Chen D, Jiang Y, Zhang Q, Zhang L, Tu PF (2013) Identification and quantification of 5,6,7,8-tetrahydro-2-(2-phenylethyl)chromones in Chinese eaglewood by HPLC with diode array detection and MS. J Sep Sci 36:3733–3740CrossRef
15.
Zurück zum Zitat Uchino S, Takahashi S, Oguri N, Maoka T, Kozuka M, Shimada Y, Hashimoto K (1998) Compositional analysis of the fragrance gas from agarwood by using curie-point pyrolysis-GC/MS and comnustion-GC/MS. Chromatography 19:3 Uchino S, Takahashi S, Oguri N, Maoka T, Kozuka M, Shimada Y, Hashimoto K (1998) Compositional analysis of the fragrance gas from agarwood by using curie-point pyrolysis-GC/MS and comnustion-GC/MS. Chromatography 19:3
16.
Zurück zum Zitat Yagura T, Shibayama N, Ito M, Kiuchi F, Honda G (2005) Three novel diepoxy tetrahydrochromones from agarwood artificially produced by intentional wounding. Tetrahedron Lett 46:4395–4398CrossRef Yagura T, Shibayama N, Ito M, Kiuchi F, Honda G (2005) Three novel diepoxy tetrahydrochromones from agarwood artificially produced by intentional wounding. Tetrahedron Lett 46:4395–4398CrossRef
17.
Zurück zum Zitat Okudera Y, Ito M (2009) Production of agarwood fragrant constituents in Aquilaria calli and cell suspension cultures. Plant Biotechnol 26:307–315CrossRef Okudera Y, Ito M (2009) Production of agarwood fragrant constituents in Aquilaria calli and cell suspension cultures. Plant Biotechnol 26:307–315CrossRef
Metadaten
Titel
Agarotetrol: a source compound for low molecular weight aromatic compounds from agarwood heating
verfasst von
Sakura Takamatsu
Michiho Ito
Publikationsdatum
20.02.2018
Verlag
Springer Singapore
Erschienen in
Journal of Natural Medicines / Ausgabe 2/2018
Print ISSN: 1340-3443
Elektronische ISSN: 1861-0293
DOI
https://doi.org/10.1007/s11418-018-1185-y

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