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Biological Activity 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
HEXAHYDRO-2H-AZEPIN-2-ONE not available 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.
HYDROQUINONE IC100=2.7 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.
INDOLE-3-ACETIC-ACID not available Korhammer, S.A. and Haslinger, E. 1994. Isolation of a Biologically Active Substance from Rhizomes of Quackgrass [Elymus repens (L.) Gould]. J. Agric. Food Chem. 42: 2048-2050.
IROLONE not available Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
JUGLONE IC99=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.
L-CANALINE not available 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.
LAWSONE IC90=2.4 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.
LIMONENE not available Duke, 1992 *
MENADIONE IC50=0.18 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.
MYRICETIN IC82=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.
NAGILACTONE-E not available Hanke, F. J., Natural Products as a Resource for Biologically Active Compounds, Thesis, U. Cal (Santa Cruz), 1986, 252 pp
NIVEUSIN not available 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.
O-COUMARATE IC95=0.20 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.
O-CRESOL IC50=0.36 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.
P-COUMARATE IC50=1.2 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.
P-CRESOL IC50=1.13 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.
P-HYDROXYBENZOATE IC50=1.34 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.
PARASORBIC-ACID not available Duke, 1992 *
PARASORBIC-ACID-GLUCOSIDE not available Duke, 1992 *
PHITHOCOL IC100=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.
List of Activity Plants.
Click on column headings to sort table by that column.
Plant Name Common Name Chemical Count Total Parts Per Million
Artemisia herba-alba Desert Wormwood 2 319
Artemisia salsoloides not available 3 12, 050
Artemisia vulgaris Mugwort 6 0
Artocarpus altilis Breadfruit 1 0
Asarum canadense Wild Ginger 1 0
Asiasarum heterotropoides Asian Wild Ginger 1 0
Asiasarum sieboldii Siebold's Wild Ginger 1 0
Asimina triloba Pawpaw 3 0.5479999780654907
Aspalathus linearis Rooibos; Kaffree Tea; Red Bush Tea 6 4, 526.399999856949
Asparagus officinalis Asparagus 4 0
Astragalus membranaceus Huang-Chi; Huang Qi 4 0
Atropa bella-donna Belladonna 2 0
Avena sativa Oats 4 320
Averrhoa carambola Carambola; Star Fruit 1 0
Azadirachta indica Neem 4 2, 000
Ballota nigra Black Horehound 2 3
Baptisia tinctoria Wild Indigo 1 0
Barosma betulina Buchu 3 0
Basella alba Vinespinach 1 0
Berberis vulgaris Barberry 3 0