Myricitrin

CAS: 17912-87-7

Ref. 3D-MM08117

Produktinformation

• Name: Myricitrin
• Synonyme: 3-[(6-Deoxy-a-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-benzopyran-4-one, 17912-87-7, 3,3′,4′,5,5′,7-Hexahydroxyflavone, 3-rhamnoside, 3-O-Rhamnosylmyricetin, 3-[(6-Deoxy-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one, 4H-1-Benzopyran-4-one, 3-[(6-deoxy-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-, 4H-1-benzopyran-4-one, 3-[(6-deoxy-alpha-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-, 5,7-Dihydroxy-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-on, 5,7-Dihydroxy-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one, 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl 6-deoxy-a-L-mannopyranoside, 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl 6-deoxy-alpha-L-mannopyranoside, 5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl 6-deoxyhexopyranoside, 6-Désoxy-alpha-L-mannopyranoside de 5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphényl)-4H-chromén-3-yle, Myricetin 3-O-rhamnopyranoside, Myricetin 3-O-rhamnoside, Myricetin 3-O-α-<span class="text-smallcaps">L</span>-rhamnopyranoside, Myricetin 3-O-α-<span class="text-smallcaps">L</span>-rhamnoside, Myricetin 3-O-α-<span class="text-smallcaps">L</span>-rhamnpyronoside, Myricetin 3-O-α-rhamnopyranoside, Myricetin 3-rhamnoside, Myricetin-3-O-α-rhamnoside, Myricetin-3-O-β-rhamnopyranoside, Myricitrine, Myricitroside, NSC 19803

Beschreibung

Myricitrin is a natural compound that is found in the bark of the Myrica tree. It has been shown to have antioxidant effects and pro-apoptotic activities. Myricitrin has been shown to induce apoptosis in HL-60 cells through activation of the caspase-3 pathway, which includes cleavage of poly (ADP-ribose) polymerase and activation of caspases. In addition, myricitrin induces apoptosis by binding to DNA and inhibiting transcription. The physiological effects of myricetin are similar to those of myricitrin due to their structural similarity. However, there is no data available on the anti-inflammatory properties or hypoglycemic effect of myricetin.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 464.38 g/mol
• Formel: C₂₁H₂₀O₁₂
• Reinheit: Min. 95%
• Farbe/Form: White Powder
• InChl: InChI=1S/C21H20O12/c1-6-14(26)17(29)18(30)21(31-6)33-20-16(28)13-9(23)4-8(22)5-12(13)32-19(20)7-2-10(24)15(27)11(25)3-7/h2-6,14,17-18,21-27,29-30H,1H3/t6-,14-,17+,18+,21-/m0/s1
• InChI Key: InChIKey=DCYOADKBABEMIQ-OWMUPTOHSA-N
• SMILES: C[C@@H]1O[C@@H](Oc2c(-c3cc(O)c(O)c(O)c3)oc3cc(O)cc(O)c3c2=O)[C@H](O)[C@H](O)[C@H]1O