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.

5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-((2S,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

CAS: 51938-32-0

Formula: C₂₆H₂₈O₁₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 564.4921

Ref: IN-DA00DGR7

Schaftoside

CAS: 51938-32-0

Schaftoside

Formula: C₂₆H₂₈O₁₄

Purity: ≥95%

Molecular weight: 564.49

Ref: 54-BUP07502

Schaftoside

CAS: 51938-32-0

Formula: C₂₆H₂₈O₁₄

Purity: ≥ 97.0%

Color and Shape: Yellow powder

Molecular weight: 564.50

Ref: 7W-GY1956

Schaftoside

CAS: 51938-32-0

Schaftoside has antioxidant activity, it also can inhibit phospholipase, lipoxygenase and cyclooxygenase, three pro-inflammatory enzymes.

Formula: C₂₆H₂₈O₁₄

Purity: 95%~99%

Molecular weight: 564.496

Ref: BP-BP1260

Schaftoside

CAS: 51938-32-0

Schaftoside analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.

Formula: C₂₆H₂₈O₁₄

Purity: (HPLC) ≥90%

Color and Shape: Powder

Molecular weight: 564.5

Ref: 11-1369

Schaftoside

CAS: 51938-32-0

Formula: C₂₆H₂₈O₁₄

Molecular weight: 564.50

Ref: 4Z-S-085001

Schaftoside

CAS: 51938-32-0

Schaftoside (APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE) has antioxidant and anticancer activity.

Formula: C₂₆H₂₈O₁₄

Purity: 98% - >99.99%

Color and Shape: Solid

Molecular weight: 564.49

Ref: TM-T3898

Schaftoside

CAS: 51938-32-0

Natural glycoside

Formula: C₂₆H₂₈O₁₄

Purity: ≥ 95.0 % (HPLC)

Color and Shape: Powder

Molecular weight: 564.5

Ref: 5G-83325

Schaftoside

CAS: 51938-32-0

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.

Formula: C₂₆H₂₈O₁₄

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 564.49 g/mol

Ref: 3D-FS73932

Schaftoside

CAS: 51938-32-0

Formula: C₂₆H₂₈O₁₄

Molecular weight: 564.5

Ref: BE-RMT19830

Schaftoside

CAS: 51938-32-0

Formula: C₂₆H₂₈O₁₄

Molecular weight: 564.5

Ref: BE-RMCS043000

Schaftoside

CAS: 51938-32-0

5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-((2S,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

Formula: C₂₆H₂₈O₁₄

Purity: 98%

Molecular weight: 564.49

Ref: IN-DG689624