CAS 17912-87-7
:Miricitrina
Descrição:
Miricitrina, com o número CAS 17912-87-7, é um glicosídeo flavonoide encontrado principalmente em várias plantas, particularmente nas espécies de Myrica. É caracterizado por sua estrutura, que consiste em um aglicona de miricetina ligada a uma porção de açúcar rhamnose. Miricitrina exibe várias atividades biológicas, incluindo propriedades antioxidantes, anti-inflamatórias e potencialmente antimicrobianas, tornando-o de interesse na pesquisa farmacológica. O composto é tipicamente solúvel em solventes polares, refletindo sua natureza glicosídica, e é frequentemente estudado por seus benefícios à saúde, particularmente na medicina tradicional. Além disso, Miricitrina tem sido investigado por seu papel na proteção das células contra o estresse oxidativo e seu potencial para modular várias vias bioquímicas. Sua presença em fontes dietéticas sugere que pode contribuir para os benefícios à saúde associados a dietas baseadas em plantas. No geral, Miricitrina representa um composto significativo no campo dos produtos naturais e da fitoquímica, com pesquisas em andamento sobre suas aplicações terapêuticas.
Fórmula:C21H20O12
InChI:InChI=1/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
Chave InChI:InChIKey=DCYOADKBABEMIQ-OWMUPTOHSA-N
SMILES:O(C1=C(OC=2C(C1=O)=C(O)C=C(O)C2)C3=CC(O)=C(O)C(O)=C3)[C@H]4[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O4
Sinónimos:- 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
- Myricitrin
- Myricitrine
- Myricitroside
- NSC 19803
- 4H-1-Benzopyran-4-one, 3-[(6-deoxy-α-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-
- 3-[(6-Deoxy-α-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one
- MYRICITRIN WITH HPLC
- MIRICITRIN
- 3-[(6-Deoxy-alpha-L-Mannopyranosyloxy)]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chroMen-4-one
- CANNABISCITRIN
- 3,3′,4′,5,5′,7-Hexahydroxyflavone 3-O-rhamnoside
- Myricetin 3-O-α-L-rhamnopyranoside
- mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-
- MYRICITRIN HPLC 98+%
- YRICITRIN
- Myricitrin(Myricitrine)
- MYRICITRIN(MYRICETIN-3-O-RHAMNOSIDE)(SH)
- 5,7-dihydroxy-3-((2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-2-(3,4,5-trihydroxy-phenyl)-1-benzopyran-4-one
- 3-[(6-deoxy-alpha-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-benzopyran-4-one
- Myricitrin, froM Myrica rubra
- Myricetin 3-α-L-rhamnopyranoside
- MYRICETIN-3-O-RHAVINOSIDE
- 5,7-Dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-2-(3,4,5-trihydroxy-phenyl)-1-benzopyran-4-one
- 3',4',5,5',7-Pentahydroxy-3-(α-L-rhamnopyranosyloxy)flavone
- 4H-1-Benzopyran-4-one,3-[(6-deoxy-α-L-
- 3-[(6-deoxy-α-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-benzopyran-4-one
- Myricetrin
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10 produtos.
Myricitrin
CAS:Fórmula:C21H20O12Pureza:>98.0%(HPLC)Cor e Forma:Light yellow to Yellow to Orange powder to crystalPeso molecular:464.38Myricitrin
CAS:Myricitrin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Fórmula:C21H20O12Pureza:(HPLC) ≥99%Cor e Forma:PowderPeso molecular:464.38Myricitrin
CAS:Fórmula:C21H20O12Pureza:(HPLC) ≥ 98.0%Cor e Forma:White to light yellow powderPeso molecular:464.38Myricetrin
CAS:Myricitrin exhibits hepatoprotective, anti-inflammatory,antioxidant, anti-allergic, antinociception, anxiolytic-like, and antipsychotic-like effects. Myricitrin can be used as a drug candidate for the treatment of cardiovascular diseases, by effectively protecting cells from ox-LDL-induced endothelial cell apoptosis and reducing atherosclerotic plaque formation. Myricitrin is also a nitric oxide (NO) and protein kinase C (PKC) inhibitor that has central nervous system activity.Fórmula:C21H20O12Pureza:95%~99%Peso molecular:464.379Myricitrin
CAS:<p>Myricitrin (Myricitrine), a flavonoid compound isolated from the root bark of Myrica cerifera, exerts antinociceptive effects.</p>Fórmula:C21H20O12Pureza:99.72%Cor e Forma:Light Yellow To Off-White Crystalline PowderPeso molecular:464.38Myricitrin
CAS:Natural glycosideFórmula:C21H20O12Pureza:≥ 95.0 % (HPLC)Cor e Forma:PowderPeso molecular:464.38Myricitrin
CAS:<p>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.</p>Fórmula:C21H20O12Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:464.38 g/mol









