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Planta Med 2001; 67(5): 477-479
DOI: 10.1055/s-2001-15813
DOI: 10.1055/s-2001-15813
Letter
© Georg Thieme Verlag Stuttgart · New York
Cardanols from Leaves of Rhus thyrsiflora
Further Information
Publication History
July 28, 2000
October 29, 2000
Publication Date:
31 December 2001 (online)
Abstract
A mixture of 3-substituted alkyl- and alkenylphenols including nine new compounds (cardanols) was isolated from leaves of the Yemenian plant Rhus thyrsiflora (Anacardiaceae) and identified by GC-MS. The position of the double bond in the compounds bearing a monolefinic side chain was determined by their typical MS fragmentation patterns after hydroxylation and trimethylsilylation.
References
-
1 Frohne D, Pfänder H J.
Giftpflanzen . Ein Handbuch für Apotheker, Ärzte, Toxikologen und Biologen. Stuttgart: Wiss. Verlagsgesellschaft; 1997: 40-2 - 2 Itokawa H, Totsuka N, Nakahara K, Takeya K, Lepoittevin J-P, Asakawa Y. Antitumor principles from Ginkgo biloba . Chemical and Pharmaceutical Bulletin. 1987; 35 3016-20
- 3 Lee J S, Cho Y S, Park E J, Kim J, Oh W K, Lee H S, Ahn J S. Phospholipase Cγ1 inhibitory principles from the sarcotestas of Ginkgo biloba . Journal of Natural Products. 1998; 61 867-1
-
4 Hegnauer R.
Chemotaxonomie der Pflanzen . Band 3. Basel: Birkhäuser Verlag; 1964 90-114 Band 8. Basel: Birkhäuser Verlag; 1989 32-9 - 5 Schmidt J, Porzel A, Adam G. 3α,20-Dihydroxy-3β-epoxylupane, a triterpene from Rhus typhina . Phytochemistry. 1998; 7 2049-51
-
6 Mabberley D J.
The Plant-book . A portable dictionary of the higher plants. Cambridge: University Press; 1990: 502 -
7 Miller A G, Cope T A.
Flora of the Arabian Peninsula and Socotra . 1. Edinburgh: University Press; 1996: 22 -
8 Kiong L S, Tyman J HP.
Long-chain phenols . Part 18. Conversion of anacardiac acid into urushiol. Journal of the Chemical Society. Perkin Transactions 1; 1981;: 1942-52 -
9 Karrer W.
Konstitution und Vorkommen der organischen Pflanzenstoffe . Basel: Birkhäuser Verlag; 1958: 76 - 10 Stahl E, Keller K, Blinn C. Cardanol, a skin irritant in pink pepper. Planta Medica. 1983; 48 5-9
- 11 Du Y, Oshima R, Yamauchi Y, Kumanotani J, Miyakoshi T. Long chain phenols from the Burmese lac tree Melanorrhoea usitate . Phytochemistry. 1986; 25 2211-18
- 12 Kazlauskas R, Mulder J, Murphy P T, Wells R J. New metabolites from the brown alga Caulocystis cephalornithos . Australian Journal of Chemistry. 1980; 33 2097-2101
- 13 Jinno S, Okita T. Synthesis and structure-activity relationship of phaffiaol and related antioxidants. Chemical and Pharmaceutical Bulletin. 1998; 46 1688-94
- 14 Lamberton J A. Studies of the optically active compounds of Anacardiaceae exudates. III. The long-chain alicyclic keto alcohols from the exudate of Campnosperma auriculata Hook F. Australian Journal of Chemistry. 1958; 11 73-81
-
15 Goad L J, Akihisa T.
Analysis of sterols . Chapman & Hall, Padstow: T.J. Press; 1997: 367, 378, 412-14 -
16
NIST/EPA/NIH Mass Spectral Database (version 4.0) . 1992: ID-Nr. 53191; - 17 Bilia A R, Ciampa L, Mendez J, Morelli I. Phytochemical investigations of Licania genus. Flavonoids from Licania pyrifolia . Pharmaceutica Acta Helvetiae. 1996; 71 199-204
- 18 Ducrey B, Wolfender J L, Marston A, Hostettmann K. Analysis of flavonoid glycosides of thirteen Epilobium species (Onagraceae) by LC-UV and Thermospray LC-MS. Phytochemistry. 1995; 38 129-38
-
19 Karrer W.
Konstitution und Vorkommen der organischen Pflanzenstoffe, Ergänzungsband 2 . Basel: Birkhäuser Verlag; 1981: 350
Dr. Jürgen Schmidt
Institut für Pflanzenbiochemie
Abteilung Naturstoffchemie
Weinberg 3
06120 Halle/Saale
Germany
Email: jschmidt@ipb-halle.de
Fax: +49-345-5582-1309