Procyanidin C2
Procyanidin C2 (Procyanidine C2) is a lipid metabolism regulator and antioxidant with free radical scavenging activity. Procyanidin C2 down-regulates ACC, SREBP-1c, FAS, SCD-1 and PPARγ. Procyanidin C2 increases the level of phosphorylated AMPKα and inhibits the level of phosphorylated mTOR. Procyanidin C2 reduces lipid accumulation, alleviates oxidative stress, enhances fatty acid oxidation and improves mitochondrial function. Procyanidin C2 can be used in the research of non-alcoholic fatty liver disease.
Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.
- CAS No.: 37064-31-6
- Formule: C45H38O18
- Masse moléculaire:866.77
-
Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Activité biologique
-
Chemical Information
- Protocole
- Pureté et documentation
- Références
-
Help & FAQs
Voir tous les produits spécifiques à Isoform AMPK
More
Activité biologique
Description
In Vitro
Procyanidin C2 (10 μM) reduces lipid accumulation, TG levels, and TC levels in Oleic acid (HY-N1446)-induced HepG2 cells[1].
Procyanidin C2 (10 μM) improves redox balance in oleic acid-induced HepG2 cells by increasing SOD activity, decreasing MDA levels, and reducing intracellular and mitochondrial-derived ROS[1].
Procyanidin C2 (10 μM) improves mitochondrial function in oleic acid-induced HepG2 cells by increasing mitochondrial membrane potential and mass, and restoring mitochondrial ultrastructure[1].
Procyanidin C2 (10 μM) regulates lipid metabolism in oleic acid-induced HepG2 cells by reducing lipogenic protein expression, increasing fatty acid oxidation-related protein expression, enhancing oxidative stress response proteins, and modulating the AMPK/mTOR signaling pathway via increased p-AMPKα, increased p-JNK, and decreased p-mTOR[1].
Procyanidin C2 (fractions derived from 200 μg/mL GSPE stock; 5 min) displays obvious antioxidant activity in a cell-free ABTS radical cation scavenging assay[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 37064-31-6
-
Masse moléculaire 866.77
-
Formule C45H38O18
-
SMILES
OC1=C([C@@H](C2=C(O[C@H](C3=CC(O)=C(O)C=C3)[C@@H](O)C4)C4=C(O)C=C2O)[C@H](O)[C@@H](C5=CC(O)=C(O)C=C5)O6)C6=C([C@@H]([C@@H]([C@@H](C7=CC(O)=C(O)C=C7)O8)O)C(C8=CC(O)=C9)=C9O)C(O)=C1
-
Synonyms
Procyanidine C2
-
Structure Classification
-
Initial Source
-
Livraison
Room temperature in continental US; may vary elsewhere.
-
Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
[1]. Tie F, et al. B-Type Trimeric Procyanidins Attenuate Nonalcoholic Hepatic Steatosis Through AMPK/mTOR Signaling Pathway in Oleic Acid-Induced HepG2 Cells and High-Fat Diet- Fed Zebrafish. Plant Foods Hum Nutr. 2025;80(1):44. Published 2025 Jan 23. [Content Brief]
[2]. Gao J, et al. Bioactivity-based antioxidative components screening and evaluation in grape seed proanthocyanidin extract. J Food Sci Technol. 2017;54(9):2645-2652. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Procyanidin C2 Related Classifications
HY-N7521 Related Classifications
Powered by Bioz
Keywords