CAS 51938-32-0
:Schaftoside
Description:
Schaftoside, with the CAS number 51938-32-0, is a flavonoid glycoside primarily derived from various plant sources, particularly those in the genus *Spatholobus*. It is characterized by its structure, which typically consists of a flavonoid aglycone linked to a sugar moiety. Schaftoside exhibits several biological activities, including antioxidant, anti-inflammatory, and potential anticancer properties, making it of interest in pharmacological research. Its solubility is generally influenced by the glycosylation, which can affect its bioavailability and interaction with biological systems. Additionally, it may contribute to the flavor and color of the plants from which it is extracted. As with many flavonoids, its health benefits are attributed to its ability to scavenge free radicals and modulate various signaling pathways in cells. Research continues to explore its full potential and mechanisms of action in various therapeutic contexts.
Formula: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
InChI key: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
Synonyms:- 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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Found 9 products.
Schaftoside
CAS:Schaftoside analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C26H28O14Purity:(HPLC) ≥90%Color and Shape:PowderMolecular weight:564.5APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE
CAS:Formula:C26H28O14Purity:98%Color and Shape:SolidMolecular weight:564.4921Schaftoside
CAS:Schaftoside has antioxidant activity, it also can inhibit phospholipase, lipoxygenase and cyclooxygenase, three pro-inflammatory enzymes.Formula:C26H28O14Purity:95%~99%Molecular weight:564.496Schaftoside
CAS:<p>Schaftoside (APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE) has antioxidant and anticancer activity.</p>Formula:C26H28O14Purity:98% - >99.99%Color and Shape:SolidMolecular weight:564.49Schaftoside
CAS:Natural glycosideFormula:C26H28O14Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight: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>Formula:C26H28O14Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:564.49 g/mol








