CAS 52012-29-0: Isoschaftoside
Formula:C26H28O14
InChI:InChI=1S/C26H28O14/c27-6-13-18(32)21(35)23(37)26(40-13)16-20(34)15(25-22(36)17(31)11(30)7-38-25)19(33)14-10(29)5-12(39-24(14)16)8-1-3-9(28)4-2-8/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=OVMFOVNOXASTPA-VYUBKLCTSA-N
SMILES:OC=1C(=C2C(=C(O)C1[C@H]3[C@H](O)[C@@H](O)[C@@H](O)CO3)C(=O)C=C(O2)C4=CC=C(O)C=C4)[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O
Synonyms:- 4H-1-Benzopyran-4-one, 6-α-<span class="text-smallcaps">L</smallcap>-arabinopyranosyl-8-β-<smallcap>D</span>-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
- 6-C-α-<span class="text-smallcaps">L</smallcap>-Arabinosyl-8-C-β-<smallcap>D</span>-glucosylapigenin
- 6-α-<span class="text-smallcaps">L</smallcap>-Arabinopyranosyl-8-β-<smallcap>D</span>-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- Apigenin 6-C-α-<span class="text-smallcaps">L</smallcap>-arabinopyranoside-8-C-β-<smallcap>D</span>-glucopyranoside
- Apigenin 6-C-α-<span class="text-smallcaps">L</smallcap>-arabinoside 8-C-β-<smallcap>D</span>-glucoside
- Apigenin-6-arabinoside-8-glucoside
- Isoschaftoside
- Isoshaftoside
- iso-Schaftoside
- 4H-1-Benzopyran-4-one, 6-α-L-arabinopyranosyl-8-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
- 6-C-α-L-Arabinosyl-8-C-β-D-glucosylapigenin
- See more synonyms
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Found 9 products.
Isoschaftoside
CAS:Isoschaftoside is a bioactive flavonoid glycoside, which is derived from various plant sources, particularly those within the Fabaceae and Poaceae families. This compound is a result of the glycosylation of apigenin, a well-known flavonoid. The mode of action of isoschaftoside involves its role as a potent antioxidant and anti-inflammatory agent. It achieves this by scavenging free radicals and modulating inflammatory pathways, thus contributing to cellular protection and immune response regulation. The uses and applications of isoschaftoside are significant in the realm of biochemistry and pharmacology. Due to its antioxidant properties, it is extensively studied for its potential in mitigating oxidative stress-related conditions. Additionally, its anti-inflammatory effects are of interest in developing treatments for inflammatory diseases. Research also explores its antitumor and antimicrobial activities, as its presence in traditional medicine hints at a broader therapeutic potential. Scientists continue to investigate its efficacy and underlying mechanisms to unlock its full spectrum of applications in drug development and nutritional science.Formula:C26H28O14Purity:Min. 97 Area-%Color and Shape:PowderMolecular weight:564.49 g/molIsoschaftoside
CAS:Isoschaftoside is used as an intercrop due to its allelopathic inhibition of parasitism by Striga hermonthica, an obligate parasitic weed that can devastate theFormula:C26H28O14Purity:99.57% - 99.96%Color and Shape:SolidMolecular weight:564.49Isoschaftoside
CAS:Isoschaftoside analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C26H28O14Purity:(HPLC) ≥95%Color and Shape:PowderMolecular weight:564.5Isoschaftoside
CAS:Natural glycosideFormula:C26H28O14Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:564.5
