| 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 2 x Vit. E | * |
| Antioxidant IC50=2 mg/L | * |
| 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 ED50=15 uM | * |
| 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-2-Inhibitor >2.5->22.5 uM | * |
| COX-2-Inhibitor 50 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. |
| 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 | * |