Stereochemistry | ABSOLUTE |
Molecular Formula | C21H24O6 |
Molecular Weight | 372.4117 |
Optical Activity | ( - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C[C@H]2COC(=O)[C@@H]2CC3=CC(OC)=C(O)C=C3)C=C1OC
InChI
InChIKey=NQWVSMVXKMHKTF-JKSUJKDBSA-N
InChI=1S/C21H24O6/c1-24-18-7-5-13(11-20(18)26-3)8-15-12-27-21(23)16(15)9-14-4-6-17(22)19(10-14)25-2/h4-7,10-11,15-16,22H,8-9,12H2,1-3H3/t15-,16+/m0/s1
Arctigenin is a plant lignan extracted from Arctium lappa that has been shown to have estrogenic properties. In ER-positive MCF-7 cells, arctigenin efficiently inhibited 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced cell migration and invasion. Arctigenin confers anti-metastatic effects by inhibiting MMP-9 and uPA via the Akt, NF-κB and MAPK signaling pathways on breast cancer, regardless of ER expression. Intake of arctigenin could be an effective supplement for breast cancer patients. Arctigenin is a phenylpropanoid dibenzylbutyrolactone lignan compound possessing antitumor, anti-inflammatory, anti-influenza, antioxidant, antibacterial, and hypoglycaemic activities. Arctigenin exhibited significant antiproliferative activity against CCRF-CEM cells after 72 h treatment with IC50 values of 1.21 ± 0.15 um. It arrested CCRF-CEM cells in the S phase. It induced apoptosis in CCRF-CEM cells in a concentration- and time-dependent manner. Arctigenin is a good candidate for the development of novel agents against T-cell lymphoma. Arctigenin has been found to act as an agonist of adiponectin receptor 1 (AdipoR1). Arctigenin is an antagonist of MR and effectively decreases the Na/K-ATPase 1 gene expression, thus highlighting its potential as an anti-hypertensive drug lead compound.
CNS Activity
Approval Year
Sourcing
PubMed
Patents
Sample Use Guides
GBS-01, an extract from the fruit of Arctium lappa L., an orally administered drug rich in Arctigenin, was given orally at escalating doses from 3.0 g (containing 1.0 g burdock fruit extract) to 12.0 g q.d.
Route of Administration:
Oral
Arctigenin decreased human rheumatoid arthritis fibroblast-like synoviocytes cell viability by 23, 30, and 38% at the dose of 10, 20, and 30 uM, respectively. The half maximal inhibitory concentration (IC50) of Arctigenin on RAFLSs was about 38 uM. Moreover, 9, 15, and 21% of RAFLSs are induced apoptosis by 10, 20, and 30 uM of Arctigenin.