CAS 11013-97-1: Metilhesperidina
Descripción:
Metilhesperidina, con el número CAS 11013-97-1, es un glucósido flavonoide derivado de la hesperidina, que se encuentra comúnmente en frutas cítricas. Se caracteriza por su estructura, que incluye un grupo metilo unido a la molécula de hesperidina, lo que mejora su solubilidad y biodisponibilidad. Metilhesperidina exhibe propiedades antioxidantes, contribuyendo a sus posibles beneficios para la salud, como efectos antiinflamatorios y apoyo para la salud cardiovascular. A menudo se utiliza en suplementos dietéticos y alimentos funcionales debido a su capacidad para modular diversas vías biológicas. Además, Metilhesperidina puede desempeñar un papel en la mejora de la circulación sanguínea y la reducción de la permeabilidad capilar. Su perfil de seguridad se considera generalmente favorable, aunque se necesita más investigación para comprender completamente su farmacocinética y efectos a largo plazo. Como un compuesto que ocurre de forma natural, también es de interés en los campos de la química de productos naturales y el desarrollo de nutracéuticos. En general, Metilhesperidina representa un compuesto valioso con aplicaciones prometedoras en salud y bienestar.
Fórmula:C29H36O15
InChI:InChI=1/C9H10N2O2/c1-3-11-8(12)4-6(2)7(5-10)9(11)13/h4,12H,3H2,1-2H3
SMILES:CCn1c(cc(C)c(C#N)c1=O)O
Sinónimos:- (2S)-2-(3,4-dimethoxyphenyl)-5-hydroxy-4-oxo-3,4-dihydro-2H-chromen-7-yl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside
- (2S)-2-(3,4-dimethoxyphenyl)-5-hydroxy-4-oxo-3,4-dihydro-2H-chromen-7-yl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-mannopyranoside
- 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl)-β-<smallcap>D</span>-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, monomethyl ether, (2S)-
- 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl)-β-<smallcap>D</span>-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, monomethyl ether, (S)-
- Hesperidin, methyl-
- Methyl HES
- Methyl Hesperidin
- Methylhesperidin
- 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, monomethyl ether, (S)-
- 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, monomethyl ether, (2S)-
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Encontrado 9 productos.
Methyl Hesperidine
CAS:Fórmula:C29H36O15Pureza:>90.0%(E)Forma y color:Light yellow to Brown powder to crystalPeso molecular:624.59Methyl Hesperidin
CAS:Methyl hesperidin has potentiating effect on coronary vasodilation induced by adenosine or related compounds, It caused inhibition of nitrendipine transport in the ileum and jejunum, but not in the duodenum. Methyl hesperidin exerts no obvious toxic effects in mice of either sex when administered at a level as high as 5.0% in the diet.Fórmula:C29H36O15Pureza:95%~99%Peso molecular:624.592Methyl-Hesperidin
CAS:Methyl Hesperidin, a flavanone glycoside (flavonoid) (C28H34O15), is abundant in citrus fruits. Its aglycone form is called hesperetin.Fórmula:C29H36O15Pureza:98.19% - 98.72%Forma y color:Light Yellow Crystalline Powder Slightly Bitter TastePeso molecular:624.5871Methylated Hesperidin (mixture of isomers)
CAS:Producto controladoApplications Methylated Hesperidin inhibits the phosphorylation of Akt and PKC pathway thus reducing TNF-alpha-induced VCAM-1 expression. Methylhesperidin inhibits nitrendipine transport in the ileum and jejunum, but not in the duodenum. References Nizamutdinova, I.T., et. al.: Int. Immunopharmacol., 8, 670 (2008); Rajnarayana, K., et. al.: Drug Metab. Drug Interactions, 23, 299 (2008)Fórmula:C29H36O15Forma y color:NeatPeso molecular:624.59Methyl hesperidine
CAS:Methyl hesperidine is a flavonoid derivative, which is a chemical compound sourced from citrus fruits, particularly from the peels. It is a modified form of hesperidin, a natural flavonoid found predominantly in oranges and other citrus species. The mode of action for methyl hesperidine involves its antioxidant and anti-inflammatory properties. It works by scavenging free radicals and reducing oxidative stress, which can help protect cells and tissues from damage. In terms of uses and applications, methyl hesperidine is primarily utilized in the pharmaceutical field due to its potential health benefits. It is studied for its role in improving vascular health, enhancing capillary resistance, and possibly improving circulation. Additionally, its antioxidant capacity makes it a candidate for cosmetic formulations aimed at skin protection and anti-aging treatments. Overall, methyl hesperidine's integration into products seeks to harness its bioactive properties for health and cosmetic benefits.Fórmula:C29H36O15Pureza:Min. 95%Forma y color:PowderPeso molecular:624.59 g/mol
