
CAS 130603-71-3: GLUCOSYLRUTIN
Formula:C33H40O21
InChI:InChI=1S/C33H40O21/c1-9-19(39)22(42)25(45)31(49-9)48-8-17-29(53-32-26(46)23(43)20(40)16(7-34)51-32)24(44)27(47)33(52-17)54-30-21(41)18-14(38)5-11(35)6-15(18)50-28(30)10-2-3-12(36)13(37)4-10/h2-6,9,16-17,19-20,22-27,29,31-40,42-47H,7-8H2,1H3/t9-,16+,17+,19-,20+,22+,23-,24+,25+,26+,27+,29+,31+,32+,33-/m0/s1
InChI key:InChIKey=PFPQMWRASYNLMZ-LGIMBNBCSA-N
SMILES:O(C1=C(OC=2C(C1=O)=C(O)C=C(O)C2)C3=CC(O)=C(O)C=C3)[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]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@H](O)[C@H]4O
Synonyms:- 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 6-deoxy-alpha-L-mannopyranosyl-(1->6)-[alpha-D-glucopyranosyl-(1->4)]-beta-D-glucopyranoside
- 3-(6-O-(6-Deoxy-alpha.-L-mannopyranosyl-O-(alpha.-D-glucopyranosyl)-(beta.-D-glucopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)5,7-dihydroxy-4H-1-benzopyran-4-on
- 3-[(O-6-Deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl-(1→6)-O-[α-<smallcap>D</smallcap>-glucopyranosyl-(1→4)]-β-<smallcap>D</span>-glucopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
- 4(G)-alpha-glucopyranosyl-rutin
- 4G-α-<span class="text-smallcaps">D</span>-glucopyranosylrutin
- 4H-1-Benzopyran-4-one, 3-[(O-6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl-(1→6)-O-[α-<smallcap>D</smallcap>-glucopyranosyl-(1→4)]-β-<smallcap>D</span>-glucopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-
- G-rutin
- Rutin G
- α G-Rutin
- α-Glucopyranosylrutin
- α-Glucosylrutin
- See more synonyms
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Found 2 products.
a-Glucosylrutin
CAS:a-Glucosylrutin is a flavonoid glycoside derivative, which is synthesized from rutin, a natural flavonoid extracted from plants such as buckwheat and citrus fruits, using an enzymatic glucosylation process. The incorporation of glucose enhances its stability and solubility compared to its parent compound, rutin. The mode of action of a-Glucosylrutin involves its antioxidant activity, where it scavenges free radicals and reduces oxidative stress at the cellular level. This activity mitigates damage to cells and tissues, which is crucial in various oxidative stress-related conditions. In terms of applications, a-Glucosylrutin is extensively utilized in cosmetic formulations due to its ability to protect skin cells, reduce inflammation, and enhance skin health. Its protective properties are also researched for potential roles in preventing chronic diseases related to oxidative damage. Researchers are exploring its applications in pharmaceuticals and nutraceuticals as well, given its enhanced bioavailability and efficacy as an antioxidant agent. Its multifunctional nature makes it a subject of interest for further scientific exploration in various biomedical fields.Formula:C33H40O21Purity:70%MinColor and Shape:PowderMolecular weight:772.66 g/molα-Glucosylrutin
CAS:α-Glucosylrutin is an effective antioxidant known for its activity in scavenging free radicals. Due to its high epidermal bioavailability, it is commonly utilized in studies related to skin aging.Formula:C33H40O21Color and Shape:SolidMolecular weight:772.66