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Plant Oenothera biennis (Onagraceae)

Common Names
Evening-Primrose
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
PHYTOSTEROL 0 Plant not available not available not available Duke, 1992 *
PHYTOSTEROLS 2 Plant not available not available not available Duke, 1992 *
POTASSIUM 14 Herb 12700.0 35100.0 -1.34 Duke, 1992 *
POTASSIUM 14 Seed 4600.0 7577.0 -0.44 Duke, 1992 *
PROLINE 0 Seed 5900.0 6297.0 -0.99 Duke, 1992 *
PROTEIN 0 Plant 150000.0 176054.0 0.02 Duke, 1992 *
PROTEIN 0 Cf 150000.0 176054.0 not available Duke, 1992 *
PROTOCATECHUIC-ACID 43 Plant not available not available not available Duke, 1992 *
PYROCATECHUIC-ACID 0 Plant not available not available not available Duke, 1992 *
QUERCETIN 176 Herb not available not available not available Duke, 1992 *
QUERCETIN 176 Leaf 91000.0 207000.0 3.00 Duke, 1992 *
RESIN 0 Plant not available not available not available Duke, 1992 *
SALICYLIC-ACID 34 Plant not available not available not available Duke, 1992 *
SERINE 1 Seed 8300.0 8858.0 -0.33 Duke, 1992 *
SODIUM 1 Seed not available 180.0 -0.43 Duke, 1992 *
STARCH 5 Seed not available not available not available Duke, 1992 *
STEARIC-ACID 8 Seed 1875.0 12150.0 -0.30 Duke, 1992 *
STEARIC-ACID 8 Seed Oil 5000.0 19000.0 -0.79 Duke, 1992 *
STIGMASTEROL 12 Fruit not available not available not available Duke, 1992 *
STIGMASTEROL 12 Inflorescence 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
Antihemolytic 1 Ohnishi, M., Morishita, H., Iwahashi, H., Toda, S., Shirataki, Y., Kimura, M., and Kido, R. 1993. Inhibitory Effects of Chlorogenic Acids on Linoleic Acid Peroxidation and Haemolysis. Phytochemistry. 36(3): 579-583. 1994.
Antihepatitic 1 Martindale's 29th
Antihepatoadenomic 1 Duke, 1992 *
Antihepatotic 1 Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Antihepatotoxic 8 Duke, 1992 *
Antiherpetic 7 Duke, 1992 *
Antiherpetic? 1 Duke, 1992 *
Antihistaminic 4 Duke, 1992 *
AntiHIV 7 Tan, G.T., Pezzuto, J.M., Kinghorn,* A.D., Hughes, S.H. Evaluation Of Natural Products As Inhibitors Of Human Immunodeficiency Virus Type 1 (HIV-1) Reverse Transcriptase. Journal of Natural Products, 54(1): 143-154, 1991.
Antihomocystinuric 1 Martindale's 29th
Antihydrophobic 1 Vlietinck, A.J. and Dommisse, R.A. eds. 1985. Advances in Medicinal Plant Research. Wiss. Verlag. Stuttgart.
Antihyperammonemic 1 Martindale's 29th
Antihypercholesterolemic 2 Economic & Medicinal Plant Research, 6: 189.
Antihyperglycemic 1 Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Antihyperkinetic 2 Davies, S., and Stewart, A. 1990. Nutritional Medicine. Avon Books, New York. 509pp.
Antihyperlipoproteinaemic 1 Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
Antihypertensive 9 Duke, 1992 *
Antihyperthyroid 2 Duke, 1992 *
Antihypoglycemic 1 Davies, S., and Stewart, A. 1990. Nutritional Medicine. Avon Books, New York. 509pp.
Antiichthyosic 1 Martindale's 29th