SMB01060

Phellamurin

≥90% (LC/MS-ELSD)

• Synonyme(s) : 8-Prenyldihydrokaempferol 7-glucoside, Fellavin, Flacoside
• Formule empirique (notation de Hill): C₂₆H₃₀O₁₁
• Numéro CAS: 52589-11-4
• Poids moléculaire : 518.51
• Numéro MDL: MFCD00869630
• Code UNSPSC : 12352205
• Nomenclature NACRES : NA.25

Propriétés

• Source biologique: plant
• Pureté: ≥90% (LC/MS-ELSD)
• Forme: solid
• Poids mol.: 518.51
• Solubilité: water: slightly soluble
• Application(s): metabolomics; vitamins, nutraceuticals, and natural products
• Température de stockage: −20°C
• InChI: 1S/C26H30O11/c1-11(2)3-8-14-16(35-26-23(34)21(32)19(30)17(10-27)36-26)9-15(29)18-20(31)22(33)24(37-25(14)18)12-4-6-13(28)7-5-12/h3-7,9,17,19,21-24,26-30,32-34H,8,10H2,1-2H3/t17-,19-,21+,22+,23-,24-,26-/m1/s1
• Clé InChI: GRDZTDZJQRPNCN-YIANMRPHSA-N

Description

Description générale

Phellamurin, a trihydroxyflavanone, is a bioactive natural compound commonly sourced from Phellodendron amurense, Phellodendron chinense, and Commiphora africana plants. Current research indicates that this plant-derived metabolite acts as an inhibitor and may possess a range of biological activities, including antioxidant, anti-tumor, anti-inflammatory, and antimicrobial properties.

Application

Phellamurin is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Actions biochimiques/physiologiques

Phellamurin induces cells apoptosis, has anti-tumor activity, exhibits inhibition of intestinal P-glycoprotein and it has a role as a metabolite.

Caractéristiques et avantages

• Suitable for Biochemical and Biomedical research
• Versatile and adaptable for wide variety of laboratory and research applications

Autres remarques

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Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable