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Natural Products
Catalog No. Information
CFN93130 3'-Demethylnobiletin

3'-Demethylnobiletin has chemopreventive effects on colon carcinogenesis, it can significantly inhibit the growth of human colon cancer cells, cause cell-cycle arrest, induce apoptosis, and profoundly modulate signaling proteins related with cell proliferation and cell death. It significantly suppresses CD36 expression.
CFN90660 3-Deoxyaconitine

3-Deoxyaconitine has toxicity.
CFN92833 3-Deoxysappanchalcone

3-Deoxysappanchalcone is an effective HO-1 inducer at the translational level. 3-Deoxysappanchalcone has anti-inflammatory, and anti-influenza virus activities, the mechanism involved anti-apoptosis and anti-inflammation activities in vitro. It has inhibitory activity on MMP-9 expression and production in TNF-α-treated cells, is mediated by the suppression of AP-1 and NF-κB activation.
CFN99229 3-Deoxysappanone B

3-Deoxysappanone B has vasorelaxation effects, it can mediate endothelium- independent vasodilator action in rat thoracic aortic rings.
CFN98851 3-Epicorosolic acid

3-Epicorosolic acid has a potent inhibitory effect on Epstein-Barr virus early antigen (EBV-EA) induction, it has potential anti-inflammatory activities as well as cancer chemopreventive activity.3-Epicorosolic acid shows both potent α-glucosidase and protein tyrosine phosphatase 1B (PTP1B) inhibitory activities with IC50 values of 30.18 and 4.08 μg/ml respectively.
CFN92738 3-Epidehydropachymic acid

Reference standards.
CFN92743 3-Epidehydrotumulosic acid

3-Epidehydrotumulosic acid has inhibitory activity against AAPH-induced lysis of red blood cells.
CFN97238 3-Epikatonic acid

Epikatonic acid shows less active against T. (S.) cruzi trypanosome.
CFN92068 3-Epioleanolic acid

3-Epioleanolic acid and oleanonic acid possess varying degrees of agonist activity on uterine smooth muscle with minor changes in the molecular structure affecting its intrinsic activity on uterine muscle.
CFN92196 3-Epiursolic acid

3-Epiursolic acid may have antiinflammatory activity, it shows inhibition on Cathepsins L (catL), the IC50 value of 6.5 uM, cathepsins L (catL) and B play an important role in tumor progression and have been considered promising therapeutic targets in the development of novel anticancer agents.