Common Names
Common Yew
How this plant is used
Medicinal
Select a Results View:
Chemical Name | Activity Count | Plant Part | Low Parts Per Million | High Parts Per Million | Standard Deviation | Reference |
---|---|---|---|---|---|---|
CEPHALOMANINE | 0 | Stem Bark | not available | not available | not available | Duke, 1992 * |
CEPHALOMANNINE | 3 | Stem Bark | not available | not available | not available | Duke, 1992 * |
CHINIC-ACID | 0 | Leaf | 0.0 | 0.2 | not available | Duke, 1992 * |
CINNAMIC-ACID | 18 | Leaf | 4.0 | 595.0 | 1.00 | Duke, 1992 * |
ECDYSTERONE | 4 | Leaf | not available | not available | not available | Duke, 1992 * |
EPHEDRINE | 49 | Leaf | not available | not available | not available | Duke, 1992 * |
ESCHESCHOLTZXANTHONE | 0 | Fruit | not available | not available | not available | Duke, 1992 * |
FERREDOXIN | 0 | Leaf | not available | not available | not available | Duke, 1992 * |
FERULIC-ACID | 61 | Leaf | 0.1 | 3.5 | -0.80 | Duke, 1992 * |
FORMIC-ACID | 13 | Leaf | not available | not available | not available | Duke, 1992 * |
GALLIC-ACID | 62 | Leaf | 0.0 | 0.3 | -0.87 | Duke, 1992 * |
GAMMA-RESORCYLIC-ACID | 0 | Leaf | 0.0 | 28.0 | not available | Duke, 1992 * |
GENTISIC-ACID | 8 | Leaf | 0.0 | 11.0 | -1.00 | Duke, 1992 * |
GINKGETIN | 11 | Leaf | not available | not available | not available | Duke, 1992 * |
GINKGETIN | 11 | Twig | not available | not available | not available | Duke, 1992 * |
HCN | 9 | Leaf | 12.0 | 39.0 | -1.14 | Duke, 1992 * |
HOMOPROTOCATECHUIC-ACID | 0 | Leaf | 0.0 | 4.0 | not available | Duke, 1992 * |
ISOLARICIRESINOL | 0 | Wood | not available | not available | not available | Duke, 1992 * |
ISOTAXIRESINOL | 0 | Wood | not available | not available | not available | Duke, 1992 * |
ISOTAXIRESINOL-6-METHYL-ETHER | 0 | Wood | not available | not available | not available | Duke, 1992 * |
Activity | Chemical Count | Reference |
---|---|---|
Antihemolytic | 1 | Ohnishi, M., Morishita, H., Iwahashi, H., Toda, S., Shirataki, Y., Kimura, M., and Kido, R. 1993. Inhibitory Effects of Chlorogenic Acids on Linoleic Acid Peroxidation and Haemolysis. Phytochemistry. 36(3): 579-583. 1994. |
Antihemorrhoidal | 1 | Martindale's 29th |
Antihepatoadenomic | 1 | Duke, 1992 * |
Antihepatotoxic | 5 | Duke, 1992 * |
Antiherpetic | 6 | Duke, 1992 * |
Antihiccup | 1 | Martindale's 29th |
Antihistaminic | 3 | Duke, 1992 * |
AntiHIV | 3 | Duke, 1992 * |
AntiHSV-1 | 1 | Duke, 1992 * |
Antihypercholesterolemic | 1 | Economic & Medicinal Plant Research, 6: 189. |
Antihyperkeratotic | 1 | Duke, 1992 * |
Antihyperlipoproteinaemic | 1 | Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. |
Antihyperthyroid | 1 | Duke, 1992 * |
Antiichthyosic | 1 | Martindale's 29th |
Antiichythyotic | 1 | Pizzorno, J.E. and Murray, M.T. 1985. A Textbook of Natural Medicine. John Bastyr College Publications, Seattle, Washington (Looseleaf). |
Antiinflammatory | 12 | Duke, 1992 * |
Antiischemic | 1 | Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. |
AntiLegionella | 2 | Duke, 1992 * |
Antileishmanic | 1 | Duke, 1992 * |
Antileukemic | 7 | Duke, 1992 * |