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Chemical structure of CAS 27200-12-0

(+)-Dihydromyricetin

In Stock•Starting at $8 for 5 mg•Purity ≥ 97%
CAS No.27200-12-0
MDL No.MFCD00189451
MFC15H12O8
MW320.25
InChI KeyKJXSIXMJHKAJOD-LSDHHAIUSA-N

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
5 mg98%$8In Stock
1 g98%$8In Stock
5 g98%$22In Stock
10 g98%$37In Stock
25 g98%$72In Stock
1 kg97%$199In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

(+)-Dihydromyricetin is an optically active form of dihydromyricetin with (2R,3R) configuration. It functions as a metabolite, antioxidant, and antineoplastic agent. It is a secondary alpha-hydroxy ketone and an enantiomer of (-)-dihydromyricetin.

CAS No.27200-12-0
Product Name(+)-Dihydromyricetin

Associated Conditions

type 2 diabetes mellitus·alcohol-related disorders
* The information provided here is compiled from public sources and is for reference only.

Related Articles

Studies related to this compound and its mechanism of action

Dihydromyricetin inhibits cancer cell migration and matrix metalloproteinases-2 expression in human nasopharyngeal carcinoma through extracellular signal-regulated kinase signaling pathway.

Environmental toxicology • Vol. 37, Issue 5 • 2022
PMID: 35112788DOI: 10.1002/tox.23480

Structure-activity relationship and mechanism of flavonoids on the inhibitory activity of P-glycoprotein (P-gp)-mediated transport of rhodamine123 and daunorubicin in P-gp overexpressed human mouth epidermal carcinoma (KB/MDR) cells.

Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association • Vol. 155 • 2021
PMID: 34217736DOI: 10.1016/j.fct.2021.112381

Effects of dihydromyricetin on ARPE-19 cell migration through regulating matrix metalloproteinase-2 expression.

Environmental toxicology • Vol. 33, Issue 12 • 2018
PMID: 30259634DOI: 10.1002/tox.22637

Dihydromyricetin modulates p62 and autophagy crosstalk with the Keap-1/Nrf2 pathway to alleviate ethanol-induced hepatic injury.

Toxicology letters • Vol. 274 • 2017
PMID: 28419832DOI: 10.1016/j.toxlet.2017.04.009

Documentation

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