Common Names
Hyssop
How this plant is used
Generally Recognized as Safe
Chemical Name | Activity Count | Plant Part | Low Parts Per Million | High Parts Per Million | Standard Deviation | Reference |
---|---|---|---|---|---|---|
METHYL-EUGENOL | 20 | Plant | 7.0 | 100.0 | -0.56 | Duke, 1992 * |
METHYL-EUGENOL | 20 | Shoot | 7.0 | 100.0 | -0.56 | Duke, 1992 * |
METHYL-MYRTENATE | 0 | Flower | 5.0 | 54.0 | not available | Duke, 1992 * |
METHYL-MYRTENATE | 0 | Leaf | 4.0 | 480.0 | not available | Duke, 1992 * |
METHYL-MYRTENATE | 0 | Shoot | not available | 20.0 | -0.71 | Kerrola, K., Galambosi, B. and Kallio, H. 1994. Volatile Components and Odor Intensity of Four Phenotypes of Hyssop (Hyssopus officinalis L.) J. Agric. Food Chem. 42: 776-781. |
METHYL-MYRTENATE | 0 | Shoot | not available | 30.0 | 1.41 | Kerrola, K., Galambosi, B. and Kallio, H. 1994. Volatile Components and Odor Intensity of Four Phenotypes of Hyssop (Hyssopus officinalis L.) J. Agric. Food Chem. 42: 776-781. |
MYRCENE | 22 | Shoot | 27.0 | 400.0 | 0.11 | Duke, 1992 * |
MYRTENAL | 5 | Shoot | 24.0 | 30.0 | -0.29 | Indian Perfumer, 35: 52. |
MYRTENIC-ACID | 0 | Plant | not available | not available | not available | Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp. |
MYRTENIC-ACID-METHYL-ESTER | 0 | Shoot | 8.0 | 11.0 | not available | Indian Perfumer, 35: 52. |
MYRTENIC-CIS-PINIC-ACID | 0 | Plant | not available | not available | not available | Duke, 1992 * |
MYRTENIC-CIS-PINOIC-ACID | 0 | Plant | not available | not available | not available | Duke, 1992 * |
MYRTENOIC-ACID-METHYL-ESTER | 0 | Essential Oil | not available | not available | not available | Duke, 1992 * |
MYRTENOL | 2 | Essential Oil | not available | not available | not available | Duke, 1992 * |
MYRTENOL | 2 | Flower | 16.0 | 160.0 | not available | Duke, 1992 * |
MYRTENOL | 2 | Leaf | 0.5 | 520.0 | 4.05 | Duke, 1992 * |
MYRTENOL | 2 | Shoot | not available | 170.0 | 0.03 | Kerrola, K., Galambosi, B. and Kallio, H. 1994. Volatile Components and Odor Intensity of Four Phenotypes of Hyssop (Hyssopus officinalis L.) J. Agric. Food Chem. 42: 776-781. |
MYRTENOL | 2 | Shoot | not available | 190.0 | 0.07 | Kerrola, K., Galambosi, B. and Kallio, H. 1994. Volatile Components and Odor Intensity of Four Phenotypes of Hyssop (Hyssopus officinalis L.) J. Agric. Food Chem. 42: 776-781. |
MYRTENOL | 2 | Shoot | not available | 200.0 | 0.08 | Kerrola, K., Galambosi, B. and Kallio, H. 1994. Volatile Components and Odor Intensity of Four Phenotypes of Hyssop (Hyssopus officinalis L.) J. Agric. Food Chem. 42: 776-781. |
MYRTENOL | 2 | Shoot | not available | 210.0 | 0.10 | Kerrola, K., Galambosi, B. and Kallio, H. 1994. Volatile Components and Odor Intensity of Four Phenotypes of Hyssop (Hyssopus officinalis L.) J. Agric. Food Chem. 42: 776-781. |
Activity | Chemical Count | Reference |
---|---|---|
Anthelmintic | 5 | Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. |
Anti-LDL | 1 | Duke, 1992 * |
Antiacetylcholine | 1 | Newall, C. A., Anderson, L. A. and Phillipson, J. D. 1996. Herbal Medicine - A Guide for Health-care Professionals. The Pharmaceutical Press, London. 296pp. |
Antiacetylcholinesterase | 9 | Duke, 1992 * |
Antiacne | 6 | Nigg, H.N. and Seigler, D.S., eds. 1992. Phytochemical Resources for Medicine and Agriculture. Plenum Press, New York. 445 pp. |
Antiadenomic | 2 | Merck 11th Edition |
Antiadenoviral | 1 | Economic & Medicinal Plant Research, 5: 207. |
Antiaggregant | 6 | Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. |
Antiaging | 1 | Duke, 1992 * |
Antiallergenic | 2 | Yakugaku Zasshi, 111: 193, 1991. |
Antiallergic | 6 | J. Food Hyg. Soc. Jap. 33(6): 569. |
Antialopecic | 1 | Duke, 1992 * |
Antialzheimeran | 4 | Duke, 1992 * |
Antialzheimeran? | 3 | Grundy, D. L. and Still, C. C., Inhibition of acetylcholinesterases by pulegone-1,2-epoxide, Oest. Biochem. & Physiol., 23, 1985, 383-8. |
Antianaphylactic | 2 | Int. J. Immunopharmacology. Vol 10: 729, 1988. |
Antiandrogenic | 1 | Malini, T. and Vanithakumari, G. 1989. Rat Toxicity Studies With B-Sitosterol. Journal of Ethnopharmacology, 28: 221-234, 1990. |
Antiarachidonate | 1 | Duke, 1992 * |
Antiarrhythmic | 4 | 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. |
Antiarthritic | 2 | Planta Medica, 57: A56, 1991. |
Antiasthmatic | 3 | Chin. J. Tuber. Respir. Dis., 4:203, 1982. |