CAS 51938-32-0
:Schaftoside
Descrição:
Schaftoside, com o número CAS 51938-32-0, é um glicosídeo flavonoide derivado principalmente de várias fontes vegetais, particularmente aquelas do gênero *Spatholobus*. É caracterizado por sua estrutura, que tipicamente consiste em uma aglicona flavonoide ligada a um moiety de açúcar. Schaftoside exibe várias atividades biológicas, incluindo propriedades antioxidantes, anti-inflamatórias e potenciais anticancerígenas, tornando-o de interesse na pesquisa farmacológica. Sua solubilidade é geralmente influenciada pela glicosilação, que pode afetar sua biodisponibilidade e interação com sistemas biológicos. Além disso, pode contribuir para o sabor e a cor das plantas de onde é extraído. Assim como muitos flavonoides, seus benefícios à saúde são atribuídos à sua capacidade de eliminar radicais livres e modular várias vias de sinalização nas células. A pesquisa continua a explorar seu potencial completo e mecanismos de ação em vários contextos terapêuticos.
Fórmula:C26H28O14
InChI:InChI=1/C26H28O14/c27-6-13-18(32)21(35)23(37)26(40-13)15-19(33)14-10(29)5-12(8-1-3-9(28)4-2-8)39-24(14)16(20(15)34)25-22(36)17(31)11(30)7-38-25/h1-5,11,13,17-18,21-23,25-28,30-37H,6-7H2/t11-,13+,17-,18+,21-,22+,23+,25-,26-/m0/s1
Chave InChI:InChIKey=MMDUKUSNQNWVET-VYUBKLCTSA-N
SMILES:OC=1C(=C2C(=C(O)C1[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)C=C(O2)C4=CC=C(O)C=C4)[C@H]5[C@H](O)[C@@H](O)[C@@H](O)CO5
Sinónimos:- 4H-1-Benzopyran-4-one, 8-α-<span class="text-smallcaps">L</smallcap>-arabinopyranosyl-6-β-<smallcap>D</span>-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
- 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl]-4H-chromen-4-one (non-preferred name)
- 6-C-β-<span class="text-smallcaps">D</smallcap>-Glucosyl-8-C-α-<smallcap>L</span>-arabinosylapigenin
- 8-α-<span class="text-smallcaps">L</smallcap>-Arabinopyranosyl-6-β-<smallcap>D</span>-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- Apigenin (8-C-α-<span class="text-smallcaps">L</smallcap>-arabinosyl) 6-C-β-<smallcap>D</span>-glucopyranoside
- Apigenin 6-C-glucoside-8-C-arabinoside
- Apigenin 6-C-β-<span class="text-smallcaps">D</smallcap>-glucoside 8-C-α-<smallcap>L</span>-arabinoside
- Apigenin 8-C-α-<span class="text-smallcaps">L</smallcap>-arabinoside 6-C-β-<smallcap>D</span>-glucoside
- Apigenin-6-Glucoside-8-Arabinoside
- Schaftoside
- Shaftoside
- 8-α-L-Arabinopyranosyl-6-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- 4H-1-Benzopyran-4-one, 8-α-L-arabinopyranosyl-6-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
- Apigenin 8-C-α-L-arabinoside 6-C-β-D-glucoside
- 6-C-β-D-Glucosyl-8-C-α-L-arabinosylapigenin
- 6-C-beta-D-Glucosyl-8-C-alpha-L-arabinosylapigenin
- Schaftoside, 98%, from Desmodium styracifolium (Osbeck) Merr.
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9 produtos.
Schaftoside
CAS:Schaftoside analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Fórmula:C26H28O14Pureza:(HPLC) ≥90%Cor e Forma:PowderPeso molecular:564.5APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE
CAS:Fórmula:C26H28O14Pureza:98%Cor e Forma:SolidPeso molecular:564.4921Schaftoside
CAS:Schaftoside has antioxidant activity, it also can inhibit phospholipase, lipoxygenase and cyclooxygenase, three pro-inflammatory enzymes.Fórmula:C26H28O14Pureza:95%~99%Peso molecular:564.496Schaftoside
CAS:Schaftoside (APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE) has antioxidant and anticancer activity.Fórmula:C26H28O14Pureza:98% - >99.99%Cor e Forma:SolidPeso molecular:564.49Schaftoside
CAS:Natural glycosideFórmula:C26H28O14Pureza:≥ 95.0 % (HPLC)Cor e Forma:PowderPeso molecular:564.5Schaftoside
CAS:<p>Schaftoside is a naturally occurring flavonoid glycoside, which is derived from a variety of plant sources, particularly within the Leguminosae and Poaceae families. As a compound, it features a structural integration of apigenin linked to two units of glucose, establishing its classification within the group of C-glycosyl flavonoids. Its mode of action involves interactions with various molecular pathways, implying antioxidant and anti-inflammatory effects. This is attributed to its capacity to scavenge free radicals and modulate signal transduction processes involving cytokines and transcription factors.</p>Fórmula:C26H28O14Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:564.49 g/mol








