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Plant Myrrhis odorata (Apiaceae)

Common Names
Garden Myrrh; Myrrh; Sweet Chervil; Sweet Cicely; Cicely
How this plant is used
Medicinal

Select a Results View:

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
CYNAROSIDE 3 Leaf not available not available not available Duke, 1992 *
CYNAROSIDE 3 Seed not available not available not available Duke, 1992 *
CYNAROSIDE 3 Shoot not available not available not available Duke, 1992 *
ELEMOL 2 Leaf Essent. Oil not available 22000.0 1.00 Duke, 1992 *
ESTRGOLE 0 Essential Oil not available 17100.0 not available Duke, 1992 *
EUGENOL-METHYL-ETHER 5 Essential Oil not available 90800.0 1.92 Hussain, R.A., et. al. 1990. Sweetening Agents of Plant Origin: Phenylpropanoid Constituents of Seven Sweet-Tasting Plants. Econ. Bot. 44 2: 174-182. Program Collab. Res. Pharm. Sci. Coll. Pharmacy Univ. Illinois at Chicago IL 60680, USA.
FUMARIC-ACID 7 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.
GAMMA-MUUROLENE 0 Leaf Essent. Oil not available 9500.0 1.00 Duke, 1992 *
GAMMA-TERPINENE 11 Leaf Essent. Oil not available 8000.0 -0.62 Duke, 1992 *
GAMMA-TERPINEOL 0 Leaf Essent. Oil not available 17500.0 not available Duke, 1992 *
GERMACRENE-D 2 Leaf Essent. Oil not available 15000.0 -0.59 Duke, 1992 *
LIMONENE 60 Essential Oil not available 2600.0 -0.72 Hussain, R.A., et. al. 1990. Sweetening Agents of Plant Origin: Phenylpropanoid Constituents of Seven Sweet-Tasting Plants. Econ. Bot. 44 2: 174-182. Program Collab. Res. Pharm. Sci. Coll. Pharmacy Univ. Illinois at Chicago IL 60680, USA.
LIMONENE 60 Plant not available not available not available Gruenwald, J. et al. 1998. PDR for Herbal Medicine. 1st ed. Medical Economics Co., Montvale, NJ. 1244 pp. (abbreviated as PHR or Physicians Herbal Reference in my mind)
LONGIFOLENE 0 Leaf Essent. Oil not available 21000.0 1.00 Duke, 1992 *
LUTEOLIN-7-O-GLUCOSIDE 2 Plant not available not available not available Gruenwald, J. et al. 1998. PDR for Herbal Medicine. 1st ed. Medical Economics Co., Montvale, NJ. 1244 pp. (abbreviated as PHR or Physicians Herbal Reference in my mind)
MYRCENE 22 Leaf Essent. Oil not available 19000.0 -0.29 Duke, 1992 *
OLEIC-ACID 18 Seed not available 53000.0 -0.54 Duke, 1992 *
OSMORHIZOLE 0 Essential Oil not available not available not available Duke, 1992 *
PETROSELINIC-ACID 0 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.
PETROSELINIC-ACID 0 Seed not available 732000.0 0.82 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
5-Alpha-Reductase-Inhibitor 1 Duke, 1992 *
Abortifacient 1 Duke, 1992 *
Acaricide 3 Duke, 1992 *
ACE-Inhibitor 4 Duke, 1992 *
AChE-Inhibitor 1 Grundy, D. L. and Still, C. C., Inhibition of acetylcholinesterases by pulegone-1,2-epoxide, Oest. Biochem. & Physiol., 23, 1985, 383-8.
Acidulant 1 Martindale's 28th
Aldose-Reductase-Inhibitor 6 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.
Allelochemic 3 Duke, 1992 *
Allelopathic 2 Wright,C.W.(Ed)2002.Medicinal&Aromatic Plants-Industrial Profiles.Artemisia.344pp.Maffei,M.(Ed)2002.Vetiveria.The Genus Vetiveria.Taylor&Francis.NY,NY.191pp.Southwell,I.,Lowe,R.(Eds)1999.Tea Tree.The Genus Melaleuca.Harwood Acad.Pub.Amsterdam,Netherlands.
Allergenic 6 Duke, 1992 *
Alpha-Reductase-Inhibitor 1 Duke, 1992 *
Analgesic 2 Kauderer, B., Zamith, H., Paumgartten, F.J.R., and Speit, G. Evaluation of the Mutagenicity of B-Myrcene in Mammalian Cells In Vitro. Environmental and Molecular Mutagenesis 18: 28-34, 1991.
Anemiagenic 1 Duke, 1992 *
Anesthetic 1 Duke, 1992 *
Antiacetylcholinesterase 5 Duke, 1992 *
Antiacne 3 Duke, 1992 *
Antiadenomic 1 Duke, 1992 *
Antiallergic 1 Duke, 1992 *
Antialopecic 1 Duke, 1992 *
Antialzheimeran? 1 Grundy, D. L. and Still, C. C., Inhibition of acetylcholinesterases by pulegone-1,2-epoxide, Oest. Biochem. & Physiol., 23, 1985, 383-8.