PeptideDB

Dihydrocurcumin

CAS No.: 76474-56-1

Dihydrocurcumin is the main metabolite of curcumin, which can reduce fat accumulation and oxidative stress response. Dih
Sales Email:peptidedb@qq.com

This product is for research use only, not for human use. We do not sell to patients.

Description Dihydrocurcumin is the main metabolite of curcumin, which can reduce fat accumulation and oxidative stress response. Dihydrocurcumin can regulate the mRNA and protein expression levels of SREBP-1C, PNPLA3 and PPARα, increase the protein expression levels of pAKT and PI3K, and reduce the intracellular NO and ROS contents through Nrf2 signaling pathway.
In vitro Colon bacteria may mediate the transformation of curcumin, but this metabolism has not been well studied. Methods AND RESULTS: The metabolism of curcumin to Escherichia Ferguson (ATCC 35469) and two strains of Escherichia coli (ATCC 8739 and DH10B) was studied in modified colonic bacteria (mMCB) medium of porcine cecal fluid with or without medication. LC-MS analysis showed that after fermentation for 36 h, the conversion rate of curcumin was 16-37%, the conversion rate of demethoxycurcumin (DMC) was 6-16%, the conversion rate of dimethoxycurcumin (bi-DMC) was 7-15%, and the conversion rate of dimethoxycurcumin (bi-DMC) was 7-15%. The amount of curcumin degradation varies with different strains and medium. Three metabolites (dihydrocurcumin (DHC), tetrahydrocurcumin (THC) and ferulic acid (FA)) were identified in the fermentation culture of all strains. In addition, a compound of m/z [M-H](-) 470 was found and identified as curcumin-adduct (curcumin-L-cysteine) by precise mass FT-ICR-MS. Conclusion: This study provides a new scheme for the bacterial metabolism of curcumin[1].
molecular weight 370.4
Molecular formula C21H22O6
CAS 76474-56-1
Storage store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility DMSO: 22.5 mg/mL (60.7 mM), Sonication and heating to 60℃ are recommended.
References 1. Qingqing Yu, et al.Dihydrocurcumin ameliorates the lipid accumulation, oxidative stress and insulin resistance in oleic acid-induced L02 and HepG2 cells.Biomedicine & Pharmacotherapy Volume 103, July 2018, Pages 1327-1336 2. Azam Hassaninasab, et al.Discovery of the curcumin metabolic pathway involving a unique enzyme in an intestinal microorganism. Proc Natl Acad Sci U S A. 2011 Apr 19;108(16):6615-20. 3. Suryani Tan, et al. Degradation of curcuminoids by in vitro pure culture fermentation. J Agric Food Chem. 2014 Nov 12;62(45):11005-15. 4. Pierre Kamnaing.et al.Trypanocidal diarylheptanoids from Aframomum letestuianum.J Nat Prod. 2003 Mar;66(3):364-7.