CAS 51938-32-0
:Schaftoside
Descripción:
Schaftoside, con el número CAS 51938-32-0, es un glucósido flavonoide derivado principalmente de diversas fuentes vegetales, particularmente de aquellas del género *Spatholobus*. Se caracteriza por su estructura, que típicamente consiste en un aglicona flavonoide unida a un moiety de azúcar. Schaftoside exhibe varias actividades biológicas, incluyendo propiedades antioxidantes, antiinflamatorias y potenciales anticancerígenas, lo que lo hace de interés en la investigación farmacológica. Su solubilidad generalmente está influenciada por la glicosilación, que puede afectar su biodisponibilidad e interacción con sistemas biológicos. Además, puede contribuir al sabor y color de las plantas de las que se extrae. Al igual que muchos flavonoides, sus beneficios para la salud se atribuyen a su capacidad para eliminar radicales libres y modular diversas vías de señalización en las células. La investigación continúa explorando su potencial completo y mecanismos de acción en varios contextos terapéuticos.
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
Clave 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.
- Ver más sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Encontrado 9 productos.
Schaftoside
CAS:Schaftoside analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Fórmula:C26H28O14Pureza:(HPLC) ≥90%Forma y color:PowderPeso molecular:564.5APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE
CAS:Fórmula:C26H28O14Pureza:98%Forma y color: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%Forma y color:SolidPeso molecular:564.49Schaftoside
CAS:Natural glycosideFórmula:C26H28O14Pureza:≥ 95.0 % (HPLC)Forma y color: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-%Forma y color:PowderPeso molecular:564.49 g/mol








