Activity | Reference |
5-HETE-Inhibitor IC50=3-9 uM | * |
5-HT-Inhibitor IC50=3-9 uM | * |
5-Lipoxygenase-Inhibitor IC50=1-9 uM | * |
5-Lipoxygenase-Inhibitor IC50=48 uM | * |
Akt-Inhibitor | * |
Antiaggregant IC50=0.016-232 uM/L | * |
Antiaggregant IC50=100 uM | * |
Antiangiogenic | * |
Antibacterial | * |
Anticancer | * |
Anticarcinogenic | * |
Antiedemic ED50 | * |
Antieicosanoid | * |
Antiinflammatory IC50=2.6 uM | * |
Antileukemic 15-30 uM | * |
Antileukotriene IC50=1.37 uM | * |
Antilipoperoxidant IC50=2 mg/L | * |
Antimutagenic ED50=4 uM | * |
Antioxidant IC50=2 mg/L | * |
Antioxidant 2 x Vit. E | * |
Antiperoxidant | Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. |
Antiproliferant | * |
Antiprostaglandin IC50=2.6 uM | * |
Antiradicular ED50=27 uM | * |
Antiseptic | * |
Antithrombic IC50=100 uM | * |
Antitumor | * |
Antitumor (Mammary) ED50=3.1 uM | * |
Antitumor (Prostate) 25 uM | * |
Antitumor (Skin) 5+ uM | * |
Antitumor (Skin) ID68=1 uM | * |
Apoptotic IC50=15-30 uM | * |
Artemicide | * |
Beta-Glucuronidase-Inhibitor IC50=~25 uM | * |
Cardioprotective | * |
Casein-Kinase-II-Inhibitor | * |
Chemopreventive | * |
COX-1-Inhibitor 50 uM/ | Jang, M. S., Pezzuto, J. M. 1998. Resveratrol Blocks Eicosanoid Production and Chemically-Induced Cellular Transformation: Implication for Cancer Chemoprevention. Pharm Biol Suppl, 36: 28-34. |
COX-1-Inhibitor ED50=15 uM | * |
COX-2-Inhibitor 30 uM/ | Subbaramaiah, K., Michaluart, P., Chung, W. J., Dannenberg, A. J. 1998. Resveratrol Inhibits the Expression of Cyclooxygenase-2 in Human Mammary and Oral Epithelial Cells. Pharm. Biol. Suppl., 36: 35-43. |
COX-2-Inhibitor >2.5->22.5 uM | * |
COX-2-Inhibitor 50 uM/ | * |
Cyclooxygenase-Inhibitor IC50=15 uM | * |
CYP1A1-Inhibitor | * |
Differentiator IC50=18 uM | * |
Elastase-Inhibitor IC50=37 uM | * |
Estrogenic 22% of genistein | * |
Fungicide | Chemical Constituents of Oriental Herbs (3 diff. books) |
Hepatoprotective | * |
HIF-1alpha-Inhibitor | * |
Hydroperoxidase-Inhibitor | * |
Hypocholesterolemic | * |
Hypotriglyceridemic | Leung, A. Y. and Foster, S. 1995. Encyclopedia of Common Natural Ingredients 2nd Ed. John Wiley & Sons, New York. 649 pp. |
IKB-kinase-Inhibitor | * |
JNK-Inhibitor | * |
Lipolytic | Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. |
MAPK-Inhibitor | * |
NADH-Ubiquinone-Oxidoreductase-Inhibitor | * |
NF-kB-Inhibitor | * |
Ornithine-Decarboxylase-Inhibitor | * |
Pesticide | * |
Phytoalexin | * |
PKC-Inhibitor | * |
PKD-Inhibitor | * |
PTK-Inhibitor 110-263 uM | * |
Quinone-Reductase-Inducer ED100=21 uM | * |
Topoisomerase-II-Inhibitor IC50=49 uM | Sun, N. J., Woo, S. H., Cassady, J. M., Snapka, R. M. 1998. DNA Polymerase and Topoisomerase II Inhibitors From Psoralea corylifolia. J Natural Products, 61: 362-366. |
VEGF-Inhibitor | * |