Plant Pterocarpus santalinus (Fabaceae) | Dr. Duke's Phytochemical and Ethnobotanical Databases

Dr. Duke's Phytochemical and Ethnobotanical Databases

U.S. Department of Agriculture

Common Names

Red Saunders

How this plant is used

Medicinal

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List of plant chemicals.
Click on column headings to sort table by that column. *Unless otherwise noted all references are to (Duke, 1992)
Chemical Name	Activity Count	Plant Part	Low Parts Per Million	High Parts Per Million	Standard Deviation	Reference
LUPENONE	0	Bark	not available	not available	not available	Duke, 1992 *
LUPEOL	21	Bark	not available	not available	not available	Duke, 1992 *
PTEROCARPDIOLONE	0	Wood	not available	not available	not available	Duke, 1992 *
PTEROCARPIN	0	Wood	not available	2500.0	not available	Duke, 1992 *
PTEROCARPOL	0	Wood	not available	not available	not available	Duke, 1992 *
PTEROCARPTRIOL	0	Wood	not available	not available	not available	Duke, 1992 *
PTEROSTILBENE	19	Wood	not available	not available	not available	Duke, 1992 *
SANTAL	0	Wood	not available	not available	not available	Duke, 1992 *
SANTALIN	0	Wood	not available	160000.0	not available	Duke, 1992 *
SANTALIN-A	0	Wood	not available	not available	not available	Duke, 1992 *
SANTALIN-B	0	Wood	not available	not available	not available	Duke, 1992 *
STIGMASTEROL	12	Plant	not available	not available	not available	Duke, 1992 *

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List of plant activities.
Click on column headings to sort table by that column. *Unless otherwise noted all references are to (Duke, 1992)
Activity	Chemical Count	Reference
Myorelaxant	1	Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Nephrotoxic	1	Martindale's 29th
Neurogenic	1	Duke, 1992 *
NO-Inhibitor	1	Duke, 1992 *
Ovulant	1	Duke, 1992 *
Perfumery	1	Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Pesticide	8	Duke, 1992 *
Phytoalexin	2	Duke, 1992 *
Prostaglandin-Synthesis-Inhibitor	1	Huang, C., Tunon, H., Bohlin, L. 1995. Anti-Inflammatory Compounds Isolated from Menyanthes trifoliata L. Yao Hsueh Hsueh Pao, 30(8): 621-626.
Sedative	2	Duke, 1992 *
Spermicide	1	Malini, T. and Vanithakumari, G. 1989. Rat Toxicity Studies With B-Sitosterol. Journal of Ethnopharmacology, 28: 221-234, 1990.
Styptic	1	Duke, 1992 *
Termiticide	1	Mater Org (Berl), 24:301, 1989.
TOPO-2-Inhibitor	1	Duke, 1992 *
Topoisomerase-I-Inhibitor	1	Hamada, S. I., Kataoka, T., Woo, J. T., Yamada, A., Yoshida, T., Nishimura, T., Otake, N., Nagai, K. 1997. Immunosuppressive Effects by Gallic Acid and Chebulagic Acid on CTL-Mediated Cytotoxicity. Biol Pharm Bull, 20: 1017-1019.
Topoisomerase-II-Inhibitor	1	Duke, 1992 *
Ubiquiot	1	Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Ulcerogenic	1	Duke, 1992 *
Xanthine-Oxidase-Inhibitor	1	Hatano, T., Yasuhara, T., Yoshihara, R., Agata, I., Noro, T., and Okuda, T. 1989. Effects of Interaction of Tannins with Co-existing Substances.VII. Inhibitory Effects of Tannins Related Polyphenols on Xanthine Oxidase. Chem. Pharm. Bull. 38(5): 1224-1229