Lippia graveolens | Plant | Dr. Duke's Phytochemical and Ethnobotanical Databases

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Common name(s)

Oregano

How used

Medicinal

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Activities: 115

Chemicals w/Activities: 6

All Chemicals: 8

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# Activity	Chemical Name	Part Filter by plant part	Low PPM	High PPM	StdDev	^*Reference
37	CARVACROL	Leaf	--	--	--	*
Allergenic * Anesthetic * Anthelmintic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antialzheimeran? L. Gracza (1985) as cited by Buchbauer re antiacetylcholinesterase. Antiatherosclerotic IC50=5.53 uM * Antibacterial MIC 170-290 Chalchat, J.C. et Garry, R.P., Bastide, P., Fabre, F. et Malhuret, R. Correlation Composition Chimique/Activite Antimicrobienne: V - Contribution a la Comparaison de 2 Methodes de Determination Des Cmi. Plantes medicinales et phytotherapie, 25: 184-193. Antibacterial MIC=39-625 Russell, G. B., Phytochemical resources for crop protection, N. Z. J. Technol., 2, 1986, 127-134. Anticholinesterase? L. Gracza (1985) as cited by Buchbauer re antiacetylcholinesterase. Antidiuretic Lawrence Review of Natural Products, Mar-92. Antiinflammatory IC50=4 uM Antimelanomic IC50=120 uM/l * Antioxidant Jimenez, J., Navarro, M.C., Montilla, M.P., Martin, A. and Martinez, A. 1993. Thymus zygis Oil: Its Effects on CCl4-Induced Hepatotoxicity and Free Radical Scavenger Activity. JEO5: 153-8. Antioxidant (LDL) IC50=5.53 uM * Antiplaque MIC=39-625 ug/ml Osawa, K., Matsumoto, T., Maruyama, T., Takiguchi, T., Okuda, K., and Takazoe, I., Studies of the antibacterial activity of plant extracts and their constituents against periodontopathic bacteria, Bull Tokyo Dent. Coll., 31 (1), 1990, 17-21 Antiprostaglandin * Antiradicular 600 x thymol Jimenez, J., Navarro, M.C., Montilla, M.P., Martin, A. and Martinez, A. 1993. Thymus zygis Oil: Its Effects on CCl4-Induced Hepatotoxicity and Free Radical Scavenger Activity. JEO5: 153-8. Antiseptic 1.5 x phenol * Antispasmodic * Antistaphylococcic * Antistreptococcic * Antitussive Newall, C. A., Anderson, L. A. and Phillipson, J. D. 1996. Herbal Medicine - A Guide for Health-care Professionals. The Pharmaceutical Press, London. 296pp. Candidicide MIC<0.1 ug/ml * Candidicide 100-150 ug/ml * Carminative Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp. Cyclooxygenase-Inhibitor #NAME? * Enterorelaxant J. Aromatherapy 4: 22. Expectorant Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp. FLavor FEMA 10-125 Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry Fungicide Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Insectifuge * Irritant Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp. Nematicide MLC=1 mg/ml * Pesticide * Prostaglandin-Inhibitor * Tracheorelaxant * Trichomonicide LD100=150 ug/ml * Vermifuge *
0	LAPACHENOLE	Root	--	210.0	--	*
0	LAPACHENOLE	Shoot	--	40.0	--	*
56	NARINGENIN	Root	--	85.0	--	*
11B-HSD-Inhibitor * Aldose-Reductase-Inhibitor 100 uM Oliveira, T. T., Nagem, T. J., Miranda, L. C. G., Paula, V. F., Teixeira, M. A. 1997. Inhibitory Action on Aldose Reductase by Soybean Flavonoids. J Braz Chem Soc, 8(3): 211-213. Aldose-Reductase-Inhibitor 1 ug/mL Aida, K., Tawata, M., Shindo, H., Onaya, T., Sasaki, H., Yamaguchi, T., Chin, M.(Chen, Z.), and Mitsuhashi, H. 1989. Isoliquiritigenin: A New Aldose Reductase Inhibitor from Glycyrrhizae Radix. Planta Medica 56(3): 254-258. Aldose-Reductase-Inhibitor IC25=1 uM Shimizu, M., Ito, T., Terashima, S., Hayashi, T., Arisawa, M., Morita, N., Kurokawa, S., Ito, K., and Hashimoto, Y. 1984. Inhibition of Lens Aldose Reductase by Flavonoids. Phytochemistry, 23: 1885-1888. Aldose-Reductase-Inhibitor IC78=10 uM Shimizu, M., Ito, T., Terashima, S., Hayashi, T., Arisawa, M., Morita, N., Kurokawa, S., Ito, K., and Hashimoto, Y. 1984. Inhibition of Lens Aldose Reductase by Flavonoids. Phytochemistry, 23: 1885-1888. Antiacetylcholinesterase * Antiaflatoxin IC50=12 uM * Antiaflatoxin IC50=3.37 ppm * Antiaggregant Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antialzheimeran * Antiamnesic * Antiamyloid-Beta * Antibacterial MIC=250-500 ug/ml Planta Medica, 57: A43, 1991. Anticancer * Antiescherichic * Antiestrogenic * Antifibrotic * Antihepatotoxic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antiherpetic Economic & Medicinal Plant Research, 5: 197. AntiHIV IC35=200 ug/ml * Antiinflammatory 20 ppm * Antileukemic IC50=>10 ug/ml Life Sciences 55: 1061. Antimutagenic ID50=50-100 nM Maga, J.A. Contribution of Phenolic Compounds to Smoke Flavor. Phenolic Compounds in Food and Their Effects on Health, Ch.13. Antioxidant 7 x quercetin * Antiperistaltic * Antiperoxidative Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antiradicular 7 x quercetin * Antisindhis IC50=15 ug/ml * Antispasmodic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antistaphylococcic * Antitumor * Antitumor-Promoter * Antiulcer Fitoterapia No.5-1990. Antiviral IC50=15 ug/ml * Aphidifuge * Aromatase-Inhibitor IC45=1 uM/l Journal of Medicinal Food 2: 235.1999. cAMP-Phosphodiesterase-Inhibitor Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf). Cancer-Preventive Stitt, P. A. Why George Should Eat Broccoli. Dougherty Co, Milwaukee, WI, 1990, 399 pp. Candidicide * Choleretic * Cytochrome-P450-Inhibitor Pizzorno, J. 1998. Total Wellness. Prima Health, a division of Prima. Decarboxylase-Inhibitor Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Embryotoxic * Estrogenic EC50=0.1-25 uM/l * Fungicide 2.5 mM * Fungistat Weidenborner, M., Hindorf, H., Jha, H.C., and Tsotsonos, P. 1989. Antifungal Activity of Flavonoids Against Storage Fungi of the Genus Aspergillus. Phytochemistry. 29(4): 1103-1105. Hepatoprotective IC50=3.37 ppm * Hepatoprotective IC50=12 uM * Neuroprotective * P450-Inhibitor * Pesticide * Serotonin-Inhibitor Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Teratogenic * TNF-alpha-Inhibitor IC50=14.41 uM * Topoisomerase-I-Inhibitor Santti, R., Makela, S., Strauss, L., Korman, J., Kostian, M. L. 1998. Phytoestrogens: Potential Endocrine Disruptors in Males. Toxicol Ind Health, 14: 223-237. Uterotrophic EC50=0.1-25 uM/l Journal of Medicinal Food 2: 227.1999.
56	NARINGENIN	Shoot	--	70.0	-1.00	*
11B-HSD-Inhibitor * Aldose-Reductase-Inhibitor 100 uM Oliveira, T. T., Nagem, T. J., Miranda, L. C. G., Paula, V. F., Teixeira, M. A. 1997. Inhibitory Action on Aldose Reductase by Soybean Flavonoids. J Braz Chem Soc, 8(3): 211-213. Aldose-Reductase-Inhibitor 1 ug/mL Aida, K., Tawata, M., Shindo, H., Onaya, T., Sasaki, H., Yamaguchi, T., Chin, M.(Chen, Z.), and Mitsuhashi, H. 1989. Isoliquiritigenin: A New Aldose Reductase Inhibitor from Glycyrrhizae Radix. Planta Medica 56(3): 254-258. Aldose-Reductase-Inhibitor IC25=1 uM Shimizu, M., Ito, T., Terashima, S., Hayashi, T., Arisawa, M., Morita, N., Kurokawa, S., Ito, K., and Hashimoto, Y. 1984. Inhibition of Lens Aldose Reductase by Flavonoids. Phytochemistry, 23: 1885-1888. Aldose-Reductase-Inhibitor IC78=10 uM Shimizu, M., Ito, T., Terashima, S., Hayashi, T., Arisawa, M., Morita, N., Kurokawa, S., Ito, K., and Hashimoto, Y. 1984. Inhibition of Lens Aldose Reductase by Flavonoids. Phytochemistry, 23: 1885-1888. Antiacetylcholinesterase * Antiaflatoxin IC50=12 uM * Antiaflatoxin IC50=3.37 ppm * Antiaggregant Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antialzheimeran * Antiamnesic * Antiamyloid-Beta * Antibacterial MIC=250-500 ug/ml Planta Medica, 57: A43, 1991. Anticancer * Antiescherichic * Antiestrogenic * Antifibrotic * Antihepatotoxic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antiherpetic Economic & Medicinal Plant Research, 5: 197. AntiHIV IC35=200 ug/ml * Antiinflammatory 20 ppm * Antileukemic IC50=>10 ug/ml Life Sciences 55: 1061. Antimutagenic ID50=50-100 nM Maga, J.A. Contribution of Phenolic Compounds to Smoke Flavor. Phenolic Compounds in Food and Their Effects on Health, Ch.13. Antioxidant 7 x quercetin * Antiperistaltic * Antiperoxidative Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antiradicular 7 x quercetin * Antisindhis IC50=15 ug/ml * Antispasmodic Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antistaphylococcic * Antitumor * Antitumor-Promoter * Antiulcer Fitoterapia No.5-1990. Antiviral IC50=15 ug/ml * Aphidifuge * Aromatase-Inhibitor IC45=1 uM/l Journal of Medicinal Food 2: 235.1999. cAMP-Phosphodiesterase-Inhibitor Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf). Cancer-Preventive Stitt, P. A. Why George Should Eat Broccoli. Dougherty Co, Milwaukee, WI, 1990, 399 pp. Candidicide * Choleretic * Cytochrome-P450-Inhibitor Pizzorno, J. 1998. Total Wellness. Prima Health, a division of Prima. Decarboxylase-Inhibitor Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Embryotoxic * Estrogenic EC50=0.1-25 uM/l * Fungicide 2.5 mM * Fungistat Weidenborner, M., Hindorf, H., Jha, H.C., and Tsotsonos, P. 1989. Antifungal Activity of Flavonoids Against Storage Fungi of the Genus Aspergillus. Phytochemistry. 29(4): 1103-1105. Hepatoprotective IC50=3.37 ppm * Hepatoprotective IC50=12 uM * Neuroprotective * P450-Inhibitor * Pesticide * Serotonin-Inhibitor Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Teratogenic * TNF-alpha-Inhibitor IC50=14.41 uM * Topoisomerase-I-Inhibitor Santti, R., Makela, S., Strauss, L., Korman, J., Kostian, M. L. 1998. Phytoestrogens: Potential Endocrine Disruptors in Males. Toxicol Ind Health, 14: 223-237. Uterotrophic EC50=0.1-25 uM/l Journal of Medicinal Food 2: 227.1999.
9	PINOCEMBRIN	Shoot	--	105.0	-0.70	*
Anesthetic Jung, J.H., Pummangura, S., Chaichantipyuth, c., Patarapanich, C., and McLaughlin, J.L. 1989. Bioactive Constituents of Melodorum fruticosum. Phytochemistry. 29(5): 1667-1670. 1990. Antibacterial IC 3 ug/ml Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antileukemic * Antiseptic * Artemicide LC50=12 ppm Jung, J.H., Pummangura, S., Chaichantipyuth, c., Patarapanich, C., and McLaughlin, J.L. 1989. Bioactive Constituents of Melodorum fruticosum. Phytochemistry. 29(5): 1667-1670. 1990. Candidicide IC 0.1-3 mg/ml Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Cytotoxic ED50=21 * Fungicide * Pesticide *
9	PINOCEMBRIN	Root	--	95.0	--	*
Anesthetic Jung, J.H., Pummangura, S., Chaichantipyuth, c., Patarapanich, C., and McLaughlin, J.L. 1989. Bioactive Constituents of Melodorum fruticosum. Phytochemistry. 29(5): 1667-1670. 1990. Antibacterial IC 3 ug/ml Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Antileukemic * Antiseptic * Artemicide LC50=12 ppm Jung, J.H., Pummangura, S., Chaichantipyuth, c., Patarapanich, C., and McLaughlin, J.L. 1989. Bioactive Constituents of Melodorum fruticosum. Phytochemistry. 29(5): 1667-1670. 1990. Candidicide IC 0.1-3 mg/ml Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. Cytotoxic ED50=21 * Fungicide * Pesticide *
71	THYMOL	Leaf	--	--	--	*
Acaricide * Allergenic * Analgesic Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus. Ancylostomicide Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus. Anesthetic Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus. Ankylostomacide Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus. Anthelmintic Williamson, E. M. and Evans, F. J., Potter's New Cyclopaedia of Botanical Drugs and Preparations, Revised Ed., Saffron Walden, the C. W. Daniel Co., Ltd., Essex UK, 362 pp, 1988, reprint 1989. Antiacne Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp. Antiaggregant IC50=0.75 Tramil, 42: 511. Antialzheimeran? L. Gracza (1985) as cited by Buchbauer re antiacetylcholinesterase. Antiarthritic Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus. Antiatherosclerotic IC50=4 uM * Antibacterial MIC=50-400 ug/ml * Antibronchitic Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus. Anticariogenic MIC=200-400 ug/ml * Anticholinesterase L. Gracza (1985) as cited by Buchbauer re antiacetylcholinesterase. Antihalitosic American Health, 12(4): 17, 1993. Antiherpetic Martindale's 28th Antiinflammatory (=indomethacin) * Antilepric Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus. Antimelanomic IC50=120 uM/l * Antineuritic * Antioxidant 100 ppm Martindale's 28th Antioxidant (LDL) IC50=4 uM * Antiperiodontic MIC=50-200 ug/ml * Antiplaque MIC=39-625 ug/ml Osawa, K., Matsumoto, T., Maruyama, T., Takiguchi, T., Okuda, K., and Takazoe, I., Studies of the antibacterial activity of plant extracts and their constituents against periodontopathic bacteria, Bull Tokyo Dent. Coll., 31 (1), 1990, 17-21 Antiradicular EC=60 Jimenez, J., Navarro, M.C., Montilla, M.P., Martin, A. and Martinez, A. 1993. Thymus zygis Oil: Its Effects on CCl4-Induced Hepatotoxicity and Free Radical Scavenger Activity. JEO5: 153-8. Antirheumatic Williamson, E. M. and Evans, F. J., Potter's New Cyclopaedia of Botanical Drugs and Preparations, Revised Ed., Saffron Walden, the C. W. Daniel Co., Ltd., Essex UK, 362 pp, 1988, reprint 1989. Antisalmonella * Antiseptic 20 x phenol Wagner & Wolff, eds. 1977. New Natural Products (RS164. I56. 176) Antispasmodic * Antistaphylococcic * Antistreptococcic MIC=200-400 ug/ml * Antitrichinosic 5% Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus. Antitussive Iwu, M.M. 1993. Handbook of African Medicinal Plants. CRC Press, Boca Raton, FL 435 pp. Ataxigenic Zebovitz, T. C. Ed. 1989. Part VII. Flavor and Fragrance Substances, in Keith L. H. and Walters, D.B., eds. Compendium of Safety Data Sheets for Research and Industrial Chemicals. VCH Publishers, New York. 3560-4253. Candidicide 100 ug/ml (>Nystatin) * Carminative Yamamoto, A., Umemori, S., and Muranishi, S. 1993. Absorption Enhancement of Intrapulmonary Administered Insulin by Various Absorption Enhancers and Protease Inhibitors in Rats. J. Pharm. Pharmacol. 46: 14-18, 1994. Counterirritant Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp. Culicide LC50=36-49 mg/l * Cyclooxygenase-Inhibitor (=indomethacin) * Dentifrice Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry Deodorant Martindale's 28th Dermatitigenic * Enterorelaxant J. Aromatherapy 4: 22. Enterotoxic Wichtl, M. 1984. Teedrogen. Ein Handbuch fur Apotheker und Arzte. Wissenschaftliche Verlagsgesellscharft. mbH Stuttgart. 393 pp. Expectorant Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp. FLavor FEMA 2-100 Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry Fungicide Merck 11th Edition Gastroirritant Martindale's 29th Gram(+)icide MIC=200-400 ug/ml * Gram(-)icide MIC=50-200 ug/ml * Insecticide LC50=36-49 mg/l * Insecticide 0.22 uM/fly * Insectifuge * Irritant Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp. Larvicide 10 ppm Berenbaum, M. R., The natives knew, Chemtech, (May), 1990, 275-279. Larvicide 58 ppm * Larvicide LC50=36-49 mg/l * Molluscicide * Myorelaxant J. Aromatherapy 4: 22. Nematicide MLC=0.1 mg/ml Shoyakugaku Zasshi, 44: 183. Perfumery Aloe Research Council - Duke writeup of non-peer reviewd book by Coats and draft by Henry Pesticide * Sedative Zebovitz, T. C. Ed. 1989. Part VII. Flavor and Fragrance Substances, in Keith L. H. and Walters, D.B., eds. Compendium of Safety Data Sheets for Research and Industrial Chemicals. VCH Publishers, New York. 3560-4253. Sprout-Inhibitor Duke, J.A.. Personal Communication. Tracheorelaxant * Trichomonicide LD100=25 ug/ml * Urinary-Antiseptic Williamson, E. M. and Evans, F. J., Potter's New Cyclopaedia of Botanical Drugs and Preparations, Revised Ed., Saffron Walden, the C. W. Daniel Co., Ltd., Essex UK, 362 pp, 1988, reprint 1989. Varroacide * Vermicide Madaus, G. 1976. Lehrbuch der Biologischen Hilfmittel. Vol,. 1-3. 2862 pp. (+ 144 p. index). Georg Olms Verlag, Hildescheim. Reprint of 1938 Madaus.

^*Unless otherwise noted all references are to Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.

Plant Lippia graveolens (Verbenaceae)

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