SMB01075

Myrtucommulone B

≥90% (LC/MS-ELSD)

• Synonyme(s) : 6,8-dihydroxy-2,2,4,4-tetramethyl-5-(2-methylpropanoyl)-9-propan-2-yl-9H-xanthene-1,3-dione
• Formule empirique (notation de Hill): C₂₄H₃₀O₆
• Numéro CAS: 54247-23-3
• Poids moléculaire : 414.49
• Code UNSPSC : 12352205
• Nomenclature NACRES : NA.25

Propriétés

• Source biologique: plant
• Pureté: ≥90% (LC/MS-ELSD)
• Forme: solid
• Poids mol.: 414.49
• Application(s): metabolomics; vitamins, nutraceuticals, and natural products
• Température de stockage: −20°C
• InChI: 1S/C24H30O6/c1-10(2)14-15-12(25)9-13(26)16(18(27)11(3)4)19(15)30-21-17(14)20(28)23(5,6)22(29)24(21,7)8/h9-11,14,25-26H,1-8H3
• Clé InChI: AYAUOXWJIWVPSO-UHFFFAOYSA-N

Description

Description générale

Myrtucommulone B, a polyprenylated acylphloroglucinol, is a naturally occurring substance typically extracted from Myrtus communis (Myrtaceae). Previous studies have indicated that this natural compound derived from plants possesses a range of biological activities, including antibacterial, anti-inflammatory, and antioxidant properties

Application

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

Actions biochimiques/physiologiques

According to the existing research, Myrtucommulone B exhibited strong inhibition of sEH (soluble epoxide hydrolase) activity, suggesting its potential role in regulating lipid metabolism and inflammation. Further, it also showed significant inhibition of α-glucosidase activity suggesting its potential as antidiabetic and antibacterial agents.

Caractéristiques et avantages

• High quality compound suitable for multiple research applications
• Compatible with HPLC and mass spectrometry techniques

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