Details
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
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/28035371 | https://www.ncbi.nlm.nih.gov/pubmed/25922263Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/26446917
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28035371 | https://www.ncbi.nlm.nih.gov/pubmed/25922263
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/26446917
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26972612 | https://www.ncbi.nlm.nih.gov/pubmed/23926267
Curator's Comment: Arctigenin can cross the blood-brain barrier and in the brain it interacts with kainate sensitive ionotropic glutamate receptors.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL382 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25922263 |
1.21 µM [IC50] | ||
Target ID: CHEMBL1075388 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22965548 |
17.34 µM [IC50] | ||
Target ID: GO:0042533 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10632084 |
3.9 µM [IC50] | ||
Target ID: CHEMBL3392946 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23691032 |
2.2 µM [IC50] | ||
Target ID: CHEMBL1994 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26446917 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Differential in vitro anti-HIV activity of natural lignans. | 1990 Nov-Dec |
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(-)-Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase. | 1996 Jan 5 |
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Antiviral activity of berberine and related compounds against human cytomegalovirus. | 2007 Mar 15 |
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Arctigenin inhibits lipopolysaccharide-induced iNOS expression in RAW264.7 cells through suppressing JAK-STAT signal pathway. | 2011 Aug |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27685612
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
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25609147
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.
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NCI_THESAURUS |
C1145
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C93251
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DTXSID60998919
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U76MR9VS6M
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ARCTIGENIN
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7770-78-7
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64981
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ACTIVE MOIETY