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Plant Glycyrrhiza glabra (Fabaceae)

Common Names
Commom Licorice; Licorice; Smooth Licorice; Licorice-Root
How this plant is used
Generally Recognized as Safe

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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
PHENYL-ETHYL-ALCOHOL 0 Root not available not available not available Duke, 1992 *
PHENYL-PROPIONIC-ACID 1 Root not available not available not available Duke, 1992 *
PHENYL-PROPIONIC-ACID 1 Root Essent. Oil not available not available not available Duke, 1992 *
PHOSPHORUS 4 Root 124.0 790.0 -0.48 Duke, 1992 *
PINOCEMBRIN 9 Plant not available not available not available Duke, 1992 *
PINOCEMBRIN 9 Shoot 9500.0 9700.0 1.41 Duke, 1992 *
POLYSACCHARIDE 0 Shoot not available 8000.0 not available Duke, 1992 *
POTASSIUM 14 Plant not available 11400.0 -0.73 Pedersen, M. 1987. Nutritional Herbology. Pederson Publishing. Bountiful, Utah. 377 pp.
POTASSIUM 14 Root 1790.0 11400.0 -0.32 Duke, 1992 *
PRENYLLICOFLAVONE-A 0 Root not available not available not available Duke, 1992 *
PRIMULA-ACID-A 0 Root not available not available not available Duke, 1992 *
PROPIONIC-ACID 6 Root not available not available not available Duke, 1992 *
PROPIONIC-ACID 6 Root Essent. Oil not available not available not available Duke, 1992 *
PROTEIN 0 Root 17270.0 110000.0 -0.09 Duke, 1992 *
PRUNETIN 2 Leaf not available not available not available Duke, 1992 *
PRUNETIN 2 Plant not available not available not available Duke, 1992 *
PSEUDOIONONE 0 Root not available 1.0 not available Kameoka, H. and Nakai, K. 1987. Components of essential oil from the root of Glycyrrhiza-glabra. Nippon Gogeikagaku Kaishi 61(9): 1119-1122.
PYRAZOLE 0 Root not available not available not available Duke, 1992 *
PYRAZOLE 0 Root Essent. Oil not available not available not available Duke, 1992 *
QUERCETIN 176 Plant not available not available not available Stitt, Paul. Why George should eat broccoli.
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
Plasmodicide 1 Neuwinger, H. D. 1996. African Ethnobotany - Poisons and Drugs. Chapman & Hall, New York. 941 pp.
Polyamine-Synthesis-Inhibitor 2 Duke, 1992 *
Poultice 1 Martindale's 29th
Preservative 2 Merck 11th Edition
Progestational 1 Duke, 1992 *
Proliferant 1 Duke, 1992 *
Prooxidant 4 Duke, 1992 *
Propecic 1 Duke, 1992 *
Prostaglandigenic 2 Duke, 1992 *
Prostaglandin-Inhibitor 1 Duke, 1992 *
Prostaglandin-Sparer 1 Fujita, T., Nakatani, E., Funaishi, N., Sakuma, S., Fujimoto, Y. Potent inhibition of prostaglandin inactivation in rabbit gastric antral mucosal slices by selenium ions in-vitro. J. Pharm. Pharmacol. 42: 655-657, 1990.
Prostaglandin-Synthesis-Inhibitor 6 Dunstan, C. A., Liu, B., Welch, C. J., Perera, P., Bohlin, L. 1998. Alphitol, a Phenolic Substance from Alphitonia zizyphoides which Inhibits Prostaglandin Biosynthesis in vitro. Phytochemistry, 48(3): 495-497.
Protein-Kinase-C-Inhibitor 3 Naim, M., Zehavi, U., Nagy, S., and Rouseff, R.L. Hydroxycinnamic Acids as Off-Flavor Precursors in Citrus Fruits and Their Products. Phenolic Compounds in Food and Their Effects on Health, Ch.14.
Protisticide 2 Martindale's 29th
Pseudoaldosteronistic 1 Duke, 1992 *
PTK-Inhibitor 3 Duke, 1992 *
Quinone-Reductase-Inducer 5 Uda, Y., Price, K. R., Williamson, G., Rhodes, M. J. C. 1997. Induction of the Anticarcinogenic Marker Enzyme, Quinone Reductase, in Murine Hepatoma Cells In Vitro by Flavonoids. Cancer Lett., 120 (2): 213-216.
Quinone-Reductase-Inhibitor 1 Duke, 1992 *
Radioprotective 1 Duke, 1992 *
Renoirritant 1 Newall, C. A., Anderson, L. A. and Phillipson, J. D. 1996. Herbal Medicine - A Guide for Health-care Professionals. The Pharmaceutical Press, London. 296pp.