CAS 14265-53-3
:7-[[6-O-(6-desoxi-α-L-manopiranosil)-β-D-glucopiranosil]oxi]-3,5-dihidroxi-2-(3-hidroxi-4-metoxifenil)-4H-1-benzopiran-4-ona
Descripción:
La sustancia química conocida como "7-[[6-O-(6-desoxi-α-L-manopiranosil)-β-D-glucopiranosil]oxi]-3,5-dihidroxi-2-(3-hidroxi-4-metoxifenil)-4H-1-benzopiran-4-ona," con el número CAS 14265-53-3, es un glucósido flavonoide. Este compuesto presenta una estructura compleja caracterizada por un esqueleto de benzopirano, que es típico de los flavonoides, y está sustituido con múltiples grupos hidroxilo que contribuyen a sus posibles propiedades antioxidantes. La presencia de unidades de azúcares, específicamente un 6-deoxi-α-L-mannopiranosilo y una unidad de β-D-glucopiranosilo, indica que es un glucósido, lo que puede mejorar su solubilidad y biodisponibilidad. Los grupos metoxi e hidroxilo en el anillo fenílico sugieren que puede exhibir diversas actividades biológicas, incluyendo efectos antiinflamatorios y antimicrobianos. Tales compuestos son a menudo estudiados por sus posibles beneficios para la salud y aplicaciones en farmacéuticos y nutracéuticos. En general, esta sustancia ejemplifica la diversidad estructural y el potencial funcional de los derivados flavonoides en la química de productos naturales.
Fórmula:C28H32O16
InChI:InChI=1/C28H32O16/c1-9-18(31)21(34)24(37)27(41-9)40-8-16-19(32)22(35)25(38)28(44-16)42-11-6-13(30)17-15(7-11)43-26(23(36)20(17)33)10-3-4-14(39-2)12(29)5-10/h3-7,9,16,18-19,21-22,24-25,27-32,34-38H,8H2,1-2H3
Clave InChI:InChIKey=FMZXFFXOKZSIMV-NNFRCGBISA-N
SMILES:O=C1C=2C(OC(=C1O)C3=CC(O)=C(OC)C=C3)=CC(O[C@@H]4O[C@H](CO[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)[C@@H](O)[C@H](O)[C@H]4O)=CC2O
Sinónimos:- 3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-4H-chromen-7-yl 6-O-(6-deoxyhexopyranosyl)hexopyranoside
- 4H-1-Benzopyran-4-one, 7-((6-O-(6-deoxy-.alpha.-L-mannopyranosyl)-.beta.-D-glucopyranosyl)oxy)-3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-
- 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl)-β-<smallcap>D</span>-glucopyranosyl]oxy]-3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-
- 7-((6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-benzopyran-4-one
- 7-[[6-O-(6-Deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl)-β-<smallcap>D</span>-glucopyranosyl]oxy]-3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one
- Flavone, 3,3′,5,7-tetrahydroxy-4′-methoxy-, 7-[6-O-(6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl)-β-<smallcap>D</span>-glucopyranoside]
- Glucopyranoside, 3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-, beta-D-
- Glucopyranoside, 3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 6-O-(6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl)-, β-<smallcap>D</span>-
- Glucopyranoside, tamarixetin-7 6-O-(6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl)-, β-<smallcap>D</span>-
- Tamarixetin 7-beta-rutinoside
- Tamarixetin 7-rutinoside
- Tamarixetin 7-β-rutinoside
- 7-[[6-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one
- Flavone, 3,3′,5,7-tetrahydroxy-4′-methoxy-, 7-[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside]
- Glucopyranoside, 3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 6-O-(6-deoxy-α-L-mannopyranosyl)-, β-D-
- Glucopyranoside, tamarixetin-7 6-O-(6-deoxy-α-L-mannopyranosyl)-, β-D-
- 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-
- 3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one
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Tamarixetin-7-O-rutinoside
CAS:<p>Tamarixetin-7-O-rutinoside is a flavonoid glycoside, which is a natural compound derived from the Tamarix plant. In nature, it is typically isolated from species within this genus, known for its phytoactive compounds. Tamarixetin-7-O-rutinoside acts primarily through its antioxidant mechanism, which involves scavenging free radicals and reducing oxidative stress within biological systems. This activity is crucial in minimizing cellular damage and maintaining homeostasis.</p>Fórmula:C28H32O16Pureza:Min. 95%Forma y color:PowderPeso molecular:624.54 g/mol
