
CAS 1139-83-9: Urolithin B
Formula:C13H8O3
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
InChI key:InChIKey=WXUQMTRHPNOXBV-UHFFFAOYSA-N
SMILES:O=C1C=2C(C=3C(O1)=CC(O)=CC3)=CC=CC2
Synonyms:- 2-Biphenylcarboxylic acid, 2′,4′-dihydroxy-, δ-lactone
- 3-Hydroxy-6H-benzo[c]chromene-6-one
- 3-Hydroxy-6H-dibenzo[b,d]pyran-6-one
- 3-Hydroxy-benzo[c]chromen-6-one
- 3-Hydroxybenzo[c]chromen-6-one
- 3-Hydroxydibenzo-α-pyrone
- 3-Hydroxyurolithin
- 6H-Dibenzo(b,d)pyran-6-one, 3-hydroxy-
- 7-Hydroxy-3,4-benzocoumarin
- NSC 94726
- Urolithin B
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Found 9 products.
Urolithin B
CAS:Urolithin B is one of the gut microbial metabolites of ellagitannins and is found in diverse plant foods, including pomegranates, berries, walnuts, tropicalFormula:C13H8O3Purity:99.45%Color and Shape:SolidMolecular weight:212.2Urolithin B
CAS:Urolithin BFormula:C13H8O3Purity:95%Color and Shape: off-white solidMolecular weight:212.20g/molUrolithin B-13C6
CAS:Controlled ProductApplications Urolithin B-13C6 is the isotope labelled analog of Urolithin B (U847005); an intestinal microbial metabolite of ellagitannis that 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. References Kallio, T., et al.: J. Agr. Food Chem., 61, 10720 (2013); Nealmongkol, P., et al.: Tetrahedron, 69, 9277 (2013); Larrosa, M., et al.: J. Agr. Food Chem., 54, 1611 (2006); Bialonska, D., et al.: J. Agr. Food Chem., 57, 10181 (2009)Formula:C7C6H8O3Color and Shape:NeatMolecular weight:218.163-hydroxy-6H-benzo[c]chromen-6-one
CAS:Purity:95.0%Color and Shape:Solid, Light rose powderMolecular weight:212.203994750976563-Hydroxy-6H-benzo[c]chromen-6-one
CAS:3-Hydroxy-6H-benzo[c]chromen-6-one is a coumarin derivative that has been shown to have anti-inflammatory properties. It was found to inhibit the production of IL-10, an anti-inflammatory cytokine, and increase autophagy in human serum cells. This compound also inhibits the polymerase chain reaction and 3t3-l1 preadipocytes. The mechanism of action may be due to its ability to inhibit LPS induced inflammatory response by decreasing mitochondrial membrane potential and cytosolic calcium levels. 3HBCO also inhibits the synthesis of proteins involved in glucose uptake and lipid metabolism in adipocytes, which may lead to weight loss.Formula:C13H8O3Purity:Min. 95%Molecular weight:212.2 g/molRef: 3D-FH124569
Discontinued product6H-Dibenzo[b,d]pyran-6-one, 3-hydroxy-
CAS:Formula:C13H8O3Purity:97%Color and Shape:SolidMolecular weight:212.2008Urolithin B
CAS:Stability Hygroscopic Applications 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. References Kallio, T., et al.: J. Agr. Food Chem., 61, 10720 (2013); Nealmongkol, P., et al.: Tetrahedron, 69, 9277 (2013); Larrosa, M., et al.: J. Agr. Food Chem., 54, 1611 (2006); Bialonska, D., et al.: J. Agr. Food Chem., 57, 10181 (2009)Formula:C13H8O3Color and Shape:NeatMolecular weight:212.20