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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
Ruscus aculeatus Butcher's Broom; Box-Holly 1 1, 600
Ruta graveolens Rue 6 20, 000
Salix alba White Willow 5 0
Salvia canariensis Canary Island Sage 3 830.1000000014901
Salvia dorisiana 'Honduran' Sage 3 82
Salvia gilliesii 'Cordoba' Sage 3 300
Salvia officinalis Sage 6 763, 532
Salvia sclarea Clary Sage 3 27
Salvia triloba Greek Sage 2 2, 490
Sambucus canadensis American Elder; Elderberry; American Elderberry; Sweet Elder 2 360, 000
Sambucus nigra European Alder; European Elder; European Elderberry; Elder; Black Elder 4 301, 000
Sambucus simpsonii Simpson's elderberry 1 0
Sanguisorba minor Small Burnet 1 0
Sanguisorba officinalis Greater Burnet 1 0
Santalum album White Sandalwood 3 0
Santolina chamaecyparissus Lavender Cotton 2 0
Sarracenia flava not available 1 0
Sassafras albidum Sassafras 3 2, 037.6000000238419
Satureja cilicica Turkish Savory 2 265
Satureja cuneifolia Cuneate Turkish Savory 4 985