SMB01060

Phellamurin

≥90% (LC/MS-ELSD)

• Synonym(s): 8-Prenyldihydrokaempferol 7-glucoside, Fellavin, Flacoside
• Empirical Formula (Hill Notation): C₂₆H₃₀O₁₁
• CAS Number: 52589-11-4
• Molecular Weight: 518.51
• MDL number: MFCD00869630
• UNSPSC Code: 12352205
• NACRES: NA.25

Properties

• biological source: plant
• Assay: ≥90% (LC/MS-ELSD)
• form: solid
• mol wt: 518.51
• solubility: water: slightly soluble
• application(s): metabolomics; vitamins, nutraceuticals, and natural products
• storage temp.: −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
• InChI key: GRDZTDZJQRPNCN-YIANMRPHSA-N

Description

General description

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.

Biochem/physiol Actions

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

Features and Benefits

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

Other Notes

For additional information on our range of Biochemicals, please complete this form.

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable