CAS 133393-81-4: brandioside
Formula:C37H48O20
InChI:InChI=1/C37H48O20/c1-15-26(44)28(46)30(48)35(52-15)51-14-24-32(56-25(43)9-6-18-4-7-20(39)22(41)12-18)33(57-36-31(49)29(47)27(45)16(2)53-36)34(54-17(3)38)37(55-24)50-11-10-19-5-8-21(40)23(42)13-19/h4-9,12-13,15-16,24,26-37,39-42,44-49H,10-11,14H2,1-3H3/b9-6+
Synonyms:- (beta-(3',4'-Dihydroxyphenyl)ethyl)-(2-O-acetyl)-(3,6-O-di-alpha-L-rhamnopyransoyl)-(4-O-caffeoyl)-beta-D-glucopyranoside
- 2'-O-Acetylpoliumoside
- beta-D-Glucopyranoside, 2-(3,4-dihydroxyphenyl)ethyl O-6-deoxy-alpha-L-mannopyranosyl-(1-3)-O-(6-deoxy-alpha-L-mannopyranosyl-(1-6))-, 2-acetate 4-(3-(3,4-dihydroxyphenyl)-2-propenoate), (E)-
- 2-(3,4-dihydroxyphenyl)ethyl 6-deoxyhexopyranosyl-(1->3)-[6-deoxyhexopyranosyl-(1->6)]-2-O-acetyl-4-O-[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]hexopyranoside
- Brandioside
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Found 4 products.
Brandioside
CAS:Brandioside is a glycoside compound, which is derived from natural plant sources. It acts by modulating cellular signaling pathways, specifically targeting pathways involved in inflammation and oxidative stress. Through this mechanism, Brandioside exhibits potential therapeutic properties by reducing inflammatory responses and protecting against cellular damage. Its applications extend across various fields, including biomedical research focusing on inflammatory diseases and neurodegenerative disorders. Given its mechanism of action, Brandioside is particularly interesting for scientists exploring novel anti-inflammatory agents and antioxidants. Studies have demonstrated its efficacy in preclinical models, making it a promising candidate for further investigation in the development of therapeutic interventions. Researchers may leverage its properties to innovate treatments aiming to restore homeostasis in pathological conditions characterized by excessive inflammation and oxidative damage.Formula:C37H48O20Purity:Min. 95%Color and Shape:PowderMolecular weight:812.77 g/molBrandioside
CAS:Brandioside (2'-Acetilpoliumoside), estratto da Callicarpa dichotoma Raeuschel, ha attività antiossidante e può essere utilizzato nello studio del diabete.Formula:C37H48O20Purity:98.08%Color and Shape:SolidMolecular weight:812.77
