Urolithin B Chemical Properties

Melting point:

247 °C

Boiling point:

432.6±24.0 °C(Predicted)

Density 

1.395±0.06 g/cm3(Predicted)

storage temp. 

2-8°C

solubility 

DMSO: soluble5mg/mL, clear (warmed)

pka

9.03±0.20(Predicted)

form 

powder

color 

white to beige

Stability:

Hygroscopic

InChI

InChI=1S/C13H8O3/c14-8-5-6-10-9-3-1-2-4-11(9)13(15)16-12(10)7-8/h1-7,14H

InChIKey

WXUQMTRHPNOXBV-UHFFFAOYSA-N

SMILES

C12=CC(O)=CC=C1C1=CC=CC=C1C(=O)O2

LogP

2.947 (est)

Safety Information

Hazard Codes 

Xn

Risk Statements 

22

WGK Germany 

3

HazardClass 

IRRITANT

HS Code 

2932209090

Urolithin B Usage And Synthesis

Uses

Urolithin B is an intestinal microbial metabolite of ellagitannis and exhibits potent anti-oxidant and pro-oxidant activies depending on the assay system and conditions. Urolithin B can also display estrogenic and/or anti-estrogenic activity.

Definition

ChEBI: Urolithin B is a member of coumarins.

Biochem/physiol Actions

Urolithin B is a natural product with antiproliferative and antioxidant activity. Urolithin B is formed by metabolism from polyphenols found in some nuts and fruits, particularly pomegranates. Urolithin B has been shown to cross the blood brain barrier, and may have neuroprotective effects against Alzheimer′s Disease.

Synthesis

GENERAL METHODS: Urolithin A-C (30a-c, 1.0 eq.) was dissolved in methyl ether and cooled to 0 °C under argon protection. Boron tribromide (BBr3) was slowly added and the reaction progress was monitored by thin layer chromatography (TLC) until the starting material was completely consumed. Subsequently, the reaction mixture was acidified by the addition of 2N hydrochloric acid solution and extracted with ethyl acetate (EtOAc) to obtain the crude product. Finally, the crude product was purified by size exclusion chromatography to obtain the target compound 3-hydroxy-6H-benzo[c]benzopyran-6-one.

in vivo

IC 50

Human Endogenous Metabolite

References

[1] Tetrahedron, 2013, vol. 69, # 44, p. 9277 - 9283
[2] European Journal of Medicinal Chemistry, 2019, vol. 161, p. 433 - 444
[3] Journal of Organic Chemistry, 2017, vol. 82, # 10, p. 5080 - 5095
[4] ChemMedChem, 2010, vol. 5, # 9, p. 1616 - 1630

Urolithin B(1139-83-9)Related Product Information

• Urolithin C
• 3-methoxy-6H-benzo[c]chromen-6-one
• Urolithin D
• 3,8,9,10-tetrahydroxy urolithin
• Urolithin A
• 3,8,10-trihydroxy urolithin
• 3,4,8,9,10-Pentahydroxy Urolithin
• Dibenzofuran
• 1-Hydroxybenzotriazole
• 2-Benzoxazolinone