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Plant Cichorium endivia (Asteraceae)

Common Names
Endive; Escarole
How this plant is used
Food
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
CYSTINE 2 Leaf 100.0 1610.0 -1.10 Duke, 1992 *
FAT 0 Leaf 2000.0 32200.0 -0.48 Duke, 1992 *
FIBER 15 Leaf 9000.0 144927.0 -0.21 Duke, 1992 *
FOLACIN 15 Leaf 1.2 25.0 1.61 Duke, 1992 *
GLUTAMIC-ACID 8 Leaf 1660.0 26731.0 -0.61 Duke, 1992 *
GLYCINE 12 Leaf 580.0 9340.0 -0.29 Duke, 1992 *
HISTIDINE 7 Leaf 230.0 3704.0 -0.84 Duke, 1992 *
HYDROXYCINNAMIC-ACID 0 Leaf not available not available not available Duke, 1992 *
INULIN 19 Root not available not available not available Duke, 1992 *
IRON 6 Leaf 6.0 360.0 -0.01 Duke, 1992 *
ISOLEUCINE 3 Leaf 720.0 11594.0 -0.12 Duke, 1992 *
KAEMPFEROL-3-0-GLUCOSIDE 0 Leaf not available not available not available Duke, 1992 *
KAEMPFEROL-GLYCOSIDES 0 Plant not available not available not available Duke, 1992 *
KILOCALORIES 0 Leaf 170.0 2737.0 -0.45 Duke, 1992 *
LEAD 0 Leaf 4.0 4.8 -0.55 Duke, 1992 *
LEUCINE 2 Leaf 980.0 15781.0 -0.11 Duke, 1992 *
LINOLEIC-ACID 27 Leaf 750.0 12077.0 0.66 Duke, 1992 *
LITHIUM 11 Leaf 0.8 1.0 -0.51 Duke, 1992 *
LYSINE 4 Leaf 630.0 10145.0 -0.62 Duke, 1992 *
MAGNESIUM 65 Leaf 95.0 2400.0 -0.67 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
Juvabional 1 Lydon, J. & Duke, S., The potential of pesticides from plants, pp. 1-41 in Craker, L. & Simon, J., eds, Herbs, Spices & Medicinal Plants: Recent Advances in Botany, Horticulture, & Pharmacology, v. 4, Oryx Press, Phoenix, 1989, 267pp.
Keratolytic 1 Martindale's 29th
Larvistat 1 Lydon, J. & Duke, S., The potential of pesticides from plants, pp. 1-41 in Craker, L. & Simon, J., eds, Herbs, Spices & Medicinal Plants: Recent Advances in Botany, Horticulture, & Pharmacology, v. 4, Oryx Press, Phoenix, 1989, 267pp.
Laxative 5 Duke, 1992 *
Leptingenic 1 Challem, J., Berkson, Burt, and Smith, Melissa Dianne. 2000.
Syndrome X - The complete nutritional program to prevent and reservse insulin resistance. John Wiley & Sons, New York. 272 pp. $24.95
Leukotriene-Inhibitor 1 Duke, 1992 *
Lipolytic 1 Duke, 1992 *
Lipotropic 1 Merck 11th Edition
Lipoxygenase-Inhibitor 2 Oszmianski, J. and Lee, C.Y. 1990. Inhibitory Effect of Phenolics on Carotene Bleaching in Vegetables. J. Agric. Food Chem. 38: 688-690.
Lithogenic 2 Davies, S., and Stewart, A. 1990. Nutritional Medicine. Avon Books, New York. 509pp.
Litholytic 1 Duke, 1992 *
Lubricant 3 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 *
Lymphocytogenic 1 Cunane, S. and Thompson, L. U., eds. 1995. Flaxseed in Human Nutrition. AOCS Press, Champaign IL. 384 pp.
MAO-A-Inhibitor 1 Duke, 1992 *
Mast-Cell-Stabilizer 1 Duke, 1992 *
Memorigenic 1 Duke, 1992 *
Metal-Chelator 1 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 *