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Plant Tilia sp. (Tiliaceae)

Common Names
Basswood; Lime; Linden
How this plant is used
Medicinal

Select a Results View:

View the list of ubiquitous chemicals
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
PHLOBAPHENE 0 Leaf not available not available not available Duke, 1992 *
PROTEIN 0 Fruit 36000.0 113000.0 0.05 Duke, 1992 *
PROTEIN 0 Leaf 162000.0 184000.0 -0.28 Duke, 1992 *
QUERCETIN 176 Flower not available not available not available Duke, 1992 *
QUERCETIN-3-GLUCOSIDE-7-RHAMNOSIDE 0 Flower not available not available not available Duke, 1992 *
QUERCETIN-RHAMNOSIDE-XYLOSIDE 0 Flower not available not available not available Duke, 1992 *
QUERCITRIN 44 Flower not available not available not available Duke, 1992 *
SAPONIN 0 Flower not available not available not available Duke, 1992 *
SERINE 1 Flower not available not available not available Duke, 1992 *
SQUALENE 10 Wood not available not available not available Duke, 1992 *
STIGMASTANOL 0 Wood not available not available not available Duke, 1992 *
STIGMASTEROL 12 Wood not available not available not available Duke, 1992 *
SUCROSE 14 Wood not available not available not available Duke, 1992 *
SUGAR 0 Flower not available not available not available Duke, 1992 *
TANNIN 35 Flower not available not available not available Duke, 1992 *
TARAXEROL 2 Bark not available not available not available Duke, 1992 *
TERPINEOL 18 Flower not available not available not available Duke, 1992 *
TETRACOSANE 0 Flower not available not available not available Duke, 1992 *
TILIROSIDE 3 Flower not available not available not available Duke, 1992 *
TOCOPHEROL 93 Flower not available not available not available Duke, 1992 *
View the list of ubiquitous chemicals
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
Lipolytic 1 Duke, 1992 *
Lipoxygenase-Inhibitor 8 Oszmianski, J. and Lee, C.Y. 1990. Inhibitory Effect of Phenolics on Carotene Bleaching in Vegetables. J. Agric. Food Chem. 38: 688-690.
Lithogenic 1 Davies, S., and Stewart, A. 1990. Nutritional Medicine. Avon Books, New York. 509pp.
Lubricant 1 Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Lyase-Inhibitor 1 Duke, 1992 *
MAO-A-Inhibitor 2 Duke, 1992 *
MAO-Inhibitor 2 Duke, 1992 *
Mast-Cell-Stabilizer 1 Duke, 1992 *
Metal-Chelator 2 McEvily, A.J., Iyengar, R., and Gross, A.T. Inhibition of Polyphenol Oxidase by Phenolic Compounds. Phenolic Compounds in Food and Their Effects on Health, Ch.25.
Metal-Chelator (Copper) 1 Seidel, V., Verholle, M., Malard, Y., Tillequin, F., Fruchart, J-C., Duriez, P., Bailleul, F., Teissier, E. 2000. Phenylpropanoids from Ballota nigra L. Inhibit in vitro LDL Peroxidation. Phytotherapy Research, 14(2): 93-98.
Metalloproteinase-Inhibitor 1 Duke, 1992 *
Metastatic 1 Science News, 146: 421.
MMP-9-Inhibitor 1 Duke, 1992 *
Monoamine-Precursor 2 Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf).
Mosquitocide 1 Duke, 1992 *
Motor-Depressant 2 Buchbauer et al, e.g.Buchbauer et al,1993.Therapeutic properties of essential oils and fragrances. Chap.12 in Teranishi,R, Buttery,R.G and Sugisawa,H. Eds. Bioactive Volatile Compounds from Plants. ACS Symposium Series 525. Amer. Chem. Soc., Washington DC
Mucolytic 1 Martindale's 28th
Mutagenic 1 Duke, 1992 *
Mycobactericide 1 Duke, 1992 *
Myorelaxant 1 Duke, 1992 *