CAS 131086-98-1

3,4,8,9-tetrahydroxy-6H-benzo[c]chromen-6-one

Description:

3,4,8,9-tetrahydroxy-6H-benzo[c]chromen-6-one, with the CAS number 131086-98-1, is a polyphenolic compound that belongs to the class of flavonoids. This substance is characterized by its complex structure, which includes multiple hydroxyl (-OH) groups that contribute to its potential antioxidant properties. The presence of these hydroxyl groups enhances its ability to scavenge free radicals, making it of interest in various biological and pharmacological studies. Additionally, the compound's chromenone core is indicative of its potential roles in medicinal chemistry, particularly in the development of therapeutic agents. Its solubility and stability can vary depending on the solvent and environmental conditions, which is crucial for its application in research and industry. Furthermore, studies have suggested that compounds with similar structures may exhibit anti-inflammatory, anti-cancer, and neuroprotective effects, although specific biological activities of this particular compound would require further investigation to fully elucidate its potential benefits and mechanisms of action.

Formula: C₁₃H₈O₆

InChI: InChI=1/C13H8O6/c14-8-2-1-5-6-3-9(15)10(16)4-7(6)13(18)19-12(5)11(8)17/h1-4,14-17H

SMILES: c1cc(c(c2c1c1cc(c(cc1c(=O)o2)O)O)O)O

Synonyms:

• 3,4,8,9-Tetrahydroxybenzo[c]chromen-6-one
• 6H-Dibenzo(b,d)pyran-6-one, 3,4,8,9-tetrahydroxy-
• 3,4,8,9-Tetrahydroxy-6H-dibenzo[b,d]pyran-6-one
• Urolithin D

Urolithin D

CAS: 131086-98-1

Urolithin D

Purity: ≥98%

Molecular weight: 260.2g/mol

Ref: 54-BUP07164

Urolithin D

CAS: 131086-98-1

Urolithin D, an EphA receptor antagonist, is an ellagitannin colonic metabolite that inhibits EphA2 phosphorylation in prostate cancer cells.

Formula: C₁₃H₈O₆

Purity: 99.87%

Color and Shape: Solid

Molecular weight: 260.2

Ref: TM-T74005

Urolithin D

CAS: 131086-98-1

Formula: C₁₃H₈O₆

Molecular weight: 260.20

Ref: 4Z-U-100005

Urolithin D

Controlled Product

CAS: 131086-98-1

Stability Hygroscopic
Applications Urolithin D is used in biological studies to evaluate DNA gyrase inhibitory activity of ellagic acid derivatives.
References Weidner-Weels, M. A., et al: Bioorg. Med. Chem. Lett., 8, 97 (1998)

Formula: C₁₃H₈O₆

Color and Shape: Neat

Molecular weight: 260.2

Ref: TR-U847020

Urolithin D

CAS: 131086-98-1

Urolithin D is a naturally occurring compound found in foods such as pomegranates, apples, and grapes. Urolithin D has been shown to stimulate autophagy, which may be due to its ability to induce mitochondrial functions. This compound also has been shown to inhibit cancer cell proliferation in vitro assays and prostate cancer cells by binding to the glucocorticoid receptor. Urolithin D has been shown to inhibit the activity of ellagitannins, hydroxide solution, and glycosidic bonds.

Formula: C₁₃H₈O₆

Purity: Min. 95%

Molecular weight: 260.2 g/mol

Ref: 3D-GFA08698

Urolithin D

CAS: 131086-98-1

Formula: C₁₃H₈O₆

Molecular weight: 260.2

Ref: ST-EA-CP-U15003