RUTAECARPINE |
2.5 ug/ml (strong activity) | Kang, S. S., Kim, J. S., Son, K. H., Kim, H. P., Chang, H. W. 1999. Cyclooxygenase-2 Inhibitor from Evodia rutaecarpa. Nat. Prod. Sci., 5(2): 65-69. |
TRANS-RESVERATROL |
20 uM/ | Jang, M., Pezzuto, J. M. 1999. Cancer Chemorpreventive Activity of Resveratrol. Drugs Exp. Clin. Res., 25(2/3): 65-77. |
RESVERATROL |
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. |
RESVERATROL |
50 uM/ | * |
APIGENIN |
<40 uM | * |
QUERCETIN |
<40 uM | * |
RESVERATROL |
>2.5->22.5 uM | * |
FLAVOKAWAIN-B |
IC16=100 ug/ml | * |
3,4-METHYLENE-DIOXYCINNAMIC-ACID-BORNYL-ESTER |
IC18=100 ug/ml | * |
CINNAMIC-ACID-BORNYL-ESTER |
IC19=100 ug/ml | * |
LAURIC-ACID |
IC20=100 | * |
CAFFEIC-ACID |
IC32=100 uM | * |
ANTHOCYANINS |
IC47=125 ug/ml | * |
BETA-TURMERONE |
IC50=1.6 ug/ml | * |
EUGENOL |
IC50=129 uM | * |
URSOLIC-ACID |
IC50=130 uM/ | * |
CINNAMALDEHYDE |
IC50=245 uM | * |
OLEANOLIC-ACID |
IC50=295 uM/ | * |
AR-TURMERONE |
IC50=5.6 ug/ml | * |
(+)-CATECHIN |
IC50=546-5,910 uM (cf indomethacin IC50=1 uM) | * |