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Dr. Duke's Phytochemical and Ethnobotanical Databases
U.S. Department of Agriculture
  1. Home
  2. Stevia rebaudiana

Stevia rebaudiana (Asteraceae)

Common Names
Ca-A-E; Sweet Leaf of Paraguay; Stevia
How this plant is used
Medicinal

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View the list of ubiquitous chemicals
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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
ALPHA-CUBEBENE 0 Flower 17.0 -1.00 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ALPHA-CUBEBENE 0 Leaf 1.0 -0.41 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ALPHA-HUMULENE 2 Flower 260.0 -0.04 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ALPHA-HUMULENE 2 Leaf 30.0 -0.42 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ALPHA-PINENE 28 Flower 4.0 -0.81 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ALPHA-PINENE 28 Leaf 5.0 -0.22 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ALPHA-TERPINEOL 23 Flower 54.0 -0.47 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ALPHA-TERPINEOL 23 Leaf 34.0 -0.53 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ALUMINUM 5 Leaf 72.0 -0.70 Pedersen, M. 1987. Nutritional Herbology. Pederson Publishing. Bountiful, Utah. 377 pp.
ANETHOLE 36 Flower Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
ANETHOLE 36 Leaf Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
APIGENIN-4'-O-GLUCOSIDE 0 Leaf 100.0 *
ASCORBIC-ACID 112 Leaf 110.0 -0.43 Pedersen, M. 1987. Nutritional Herbology. Pederson Publishing. Bountiful, Utah. 377 pp.
ASH 0 Leaf 63000.0 130000.0 0.20 *
AUSTROINULIN 0 Flower 2100.0 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
AUSTROINULIN 0 Leaf 600.0 *
AUSTROINULIN 0 Plant *
BENZYL-ALCOHOL 9 Flower 4.0 -0.79 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
BENZYL-ALCOHOL 9 Leaf 12.0 0.08 Kinghorn, A. D. (Ed.) 2002. Medicinal and Aromatic Plants - Industrial Profiles. Stevia. The genus Stevia. Taylor & Francis. New York, NY. 211 pp.
BENZYL-ALCOHOL 9 Plant 10.0 -1.00 Hansel, R., Keller, K., Rimpler, H., and Schneider, G. eds. 1992. Hager's Handbuch der Pharmazeutischen Praxis, Drogen (A-D), 1209 pp., 1993 (E-O), 970 pp., 1994 (P-Z), 1196 pp. Springer-Verlag, Berlin.
View the list of ubiquitous chemicals
Download these results as:
CSV
EXCEL
PDF
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
Preservative 2 Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry
Prooxidant 3 *
Prostaglandin-Inhibitor 1 *
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 1 Chen, S. J., Wang, M. H., Chen, I. J. 1996. Antiplatelet and Calcium Inhibitory Properties of Eugenol and Sodium Eugenol Acetate. Gen Pharmacol, 27(4): 629-633.
Protein-Kinase-C-Inhibitor 1 *
Protisticide 1 *
Radioprotective 1 *
Refrigerant 1 Martindale's 28th
Respirainhibitor 1 Merck 11th Edition
Respirastimulant 1 Huang, K. C. 1993. The Pharmacology of Chinese Herbs. CRC Press, Boca Raton, FL 388 pp.
Rubefacient 2 *
Secretogogue 2 Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp.
Secretolytic 1 Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp.
Sedative 15 Wagner & Wolff, eds. 1977. New Natural Products (RS164. I56. 176)
Sequestrant 1 Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry
Serotoninergic 1 Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf).
Sialogogue 1 Martindale's 29th
Spasmogenic 3 *
Spermicide 1 Malini, T. and Vanithakumari, G. 1989. Rat Toxicity Studies With B-Sitosterol. Journal of Ethnopharmacology, 28: 221-234, 1990.