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Dr. Duke's Phytochemical and Ethnobotanical Databases
U.S. Department of Agriculture
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Allelochemic

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List of activity chemicals.
Click on column headings to sort table by that column. *Unless otherwise noted all references are to (Duke, 1992)
Chemical Name Dosage Reference
(-)-EPICATECHIN Hanke, F. J., Natural Products as a Resource for Biologically Active Compounds, Thesis, U. Cal (Santa Cruz), 1986, 252 pp
(20S0-4ALPHA-METHYL-24-METHYLENECHOLEST-7-EN-3BETA-OL *
1,4-NAPTHAQUINONE IC50=0.15 mM 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.
15-HYDROXY-3-DEHYDRODESOXY-FRUITICIN Rizk, A.F.M. and Al-Nowaihi, A.S., The Phytochemistry of the Horticultural Plants of Qatar, Scientific and Applied Research Centre, University of Qatar.
2',6'-DIHYDROXY-4'-METHOXYACETOPHENONE *
2,3-DIHYDROXYBENZOATE IC50=1.7 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.
2-METHOXY-1,4-NAPTHOQUINONE IC90=0.6 mM 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.
2-METHOXY-3-METHYL-NAPTHOQUINONE IC100=4 mM 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.
2-METHYL-5-METHOXY-NAPTHOQUINONE IC100=5 mM 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.
2-NAPTHOL IC50=0.2 mM 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.
4-HYDROXYBENZALDEHYDE IC50=0.38 mM 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.
4-METHOXY-1,2-NAPTHOQUINONE IC95=26 mM 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.
4-METHOXYMEDICARPIN IC83=0.8 mM 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.
5-ACETOXY-1,4-NAPTHOQUINONE IC74=5 mM 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.
5-METHOXY-1,4-NAPTHOQUINONE IC95=6 mM 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.
7-METHYLJUGLONE IC95=8 mM 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.
ALPHA-PINENE *
ALPHA-RESORCYLATE IC50=4.6 mM 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.
ARBUTIN IC51=1.1 mM 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.
BENZOATE IC50=0.51 mM 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.
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List of Activity Plants.
Click on column headings to sort table by that column.
Plant Name Common Name Chemical Count Total Parts Per Million
Angelica sinensis Dang Gui; Dong Quai; Dang Quai; Dang Qui; Dong Gui; Chinese Angelica 3 0
Aniba rosaeodora Bois-De-Rose; Cayenne Rosewood 2 0
Annona squamosa Sugar-Apple; Sweetsop 3 0
Anogeissus latifolia Gum Ghatti 3 0
Apium graveolens Celery 10 3, 850, 240
Arachis hypogaea Groundnut; Peanut 3 24
Aralia cordata Udo 2 478
Araucaria bidwillii Monkey puzzle 3 0
Arbutus unedo Arbutus; Strawberry Tree 3 54, 000
Arctium lappa Gobo; Great Burdock; Burdock 1 0
Arctostaphylos uva-ursi Bearberry; Uva Ursi 8 596, 060
Ardisia japonica Marlberry 1 0
Aristolochia serpentaria Serpentaria; Virginia Snakeroot 1 0
Armoracia rusticana Horseradish 2 0
Arnica montana Leopard's-Bane; Mountain Tobacco 1 0
Artemisia abrotanum Southernwood 4 0
Artemisia absinthium Wormwood 2 0
Artemisia annua Qinghao; Sweet Annie; Annual Mugwort (GRIN); Annual Wormwood (GRIN); Sweet Wormwood (GRIN) 7 70, 125
Artemisia capillaris Capillary Wormwood 6 0
Artemisia dracunculus Tarragon 10 11, 830