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Plant Hordeum vulgare (Poaceae)

Common Names
Barley; Barleygrass
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
(+)-CATECHIN 30 Seed not available not available not available Duke, 1992 *
(+)-CORYDINE 0 Root not available not available not available Duke, 1992 *
(+)-GLAUCINE 1 Root not available not available not available Duke, 1992 *
(R)-EPI-HETERODENDRIN 0 Sprout Seedling not available not available not available Duke, 1992 *
1,4-BENZOQUINONE 0 Leaf not available not available not available Duke, 1992 *
1,4-BENZOQUINONE 0 Root not available not available not available Duke, 1992 *
1,4-BENZOQUINONE 0 Tissue Culture not available not available not available Duke, 1992 *
1-(3-AMINO-PROPYL)-PYROLLINIUM 0 Sprout Seedling not available not available not available Duke, 1992 *
2'-DEOXYMUGINEIC ACID 0 Root not available not available not available Duke, 1992 *
2-CARBOXYARABINITOL 0 Leaf not available 814.0 1.67 Moore, B. D., Isidoro, E., Seemann, J. R. 1993. Distribution of 2-Carboxyarabinitol Among Plants. Phytochemistry 34 3: 703-707. Dept. Biochem. Univ. Nevada Reno 89557, USA.
28-ISOFUCOSTEROL 0 Embryo not available not available not available Duke, 1992 *
28-ISOFUCOSTEROL 0 Seed not available not available not available Duke, 1992 *
3-HYDROXY-MUGENIC-ACID 0 Root not available not available not available Duke, 1992 *
5,7-DIHYDROXY-3',4',5'-TRIMETHOXY-FLAVONE 0 Shoot not available not available not available Duke, 1992 *
5-HYDROXY-TRANS-FERULIC-ACID 0 Plant not available not available not available Duke, 1992 *
ABSCISIC-ACID 0 Seed not available not available not available Duke, 1992 *
ACONITIC-ACID 1 Root not available not available not available Duke, 1992 *
ACONOTIC-ACID 0 Root not available not available not available Duke, 1992 *
AESCULETIN 32 Plant not available not available not available List, P.H. and Horhammer, L., Hager's Handbuch der Pharmazeutischen Praxis, Vols. 2-6, Springer-Verlag, Berlin, 1969-1979.
AESCULETIN 32 Protoplast 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
Antipodriac 1 Davies, S., and Stewart, A. 1990. Nutritional Medicine. Avon Books, New York. 509pp.
Antipolio 1 Jim Duke's personal files.
Antipoliomyelitic 3 Davies, S., and Stewart, A. 1990. Nutritional Medicine. Avon Books, New York. 509pp.
Antipolyp 1 Duke, 1992 *
Antiporphyric 1 Martindale's 28th
Antiprogestational 1 Malini, T. and Vanithakumari, G. 1989. Rat Toxicity Studies With B-Sitosterol. Journal of Ethnopharmacology, 28: 221-234, 1990.
Antiprolactin 2 Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf).
Antiproliferant 5 Joseph, J., Nadeau, D. and Underwood, A. 2001. The Color Code. Hyperion, NY.
Antiprostaglandin 7 Duke, 1992 *
Antiprostatadenomic 1 Merck 11th Edition
Antiprostatitic 4 Duke, 1992 *
Antiprostatotic 1 Duke, 1992 *
Antipsittacotic 1 Mills, Simon and Bone, Kerry. 2000. Phytotherapy. Churchill
Livinston, Edinburgh.
Antipsoriac 3 Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf).
Antipsychotic 3 Martindale's 29th
Antipyretic 8 Economic & Medicinal Plant Research, 6: 189.
Antiradiation 1 Davies, S., and Stewart, A. 1990. Nutritional Medicine. Avon Books, New York. 509pp.
Antiradicular 17 Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
AntiRaynaud's 4 Duke, 1992 *
Antiretardation 1 Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.