SML3047
Urolithin C
≥97% (HPLC)
Synonym(s):
3,8,9-Trihydroxy-6H-benzo[c]chromen-6-one, 3,8,9-Trihydroxy-6H-dibenzo[b,d]pyran-6-one, 3,8,9-Trihydroxyurolithin
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About This Item
Empirical Formula (Hill Notation):
C13H8O5
CAS Number:
Molecular Weight:
244.20
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77
Recommended Products
Quality Level
Assay
≥97% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
−20°C
SMILES string
O=C1C2=CC(O)=C(O)C=C2C3=C(C=C(O)C=C3)O1
Biochem/physiol Actions
Urolithin C is chebulic ellagitannins metabolite that exerts antiproliferative and antioxidant activity. Urolithin C exhibit glucose dependent enhancement of insulin secretion in islet cells under normal or dysfunctional conditions. Apparently, it facilitates L-type Ca2+ channel opening and Ca2+ influx into pancreatic β-cells.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Inhae Kang et al.
Molecular nutrition & food research, 60(5), 1129-1138 (2016-02-14)
Urolithins (Uro) are ellagic acid (EA)-derived metabolites produced by gut microbes. There is a growing interest in the biological activities of Uro. Our aim was to evaluate the impacts of Uro on regulating triglyceride (TG) accumulation using cultures of primary
Morgane Bayle et al.
British journal of pharmacology, 176(20), 4065-4078 (2019-08-06)
The pharmacology of polyphenol metabolites on beta-cell function is largely undetermined. We sought to identify polyphenol metabolites that enhance the insulin-secreting function of beta-cells and to explore the underlying mechanisms. INS-1 beta-cells and rat isolated islets of Langerhans or perfused
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