CAS 29838-67-3: Astilbin
Formula:C21H22O11
InChI:InChI=1S/C21H22O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-26,28-29H,1H3/t7-,15-,17+,18+,19+,20-,21-/m0/s1
InChI key:InChIKey=ZROGCCBNZBKLEL-MPRHSVQHSA-N
SMILES:O([C@@H]1[C@H](OC=2C(C1=O)=C(O)C=C(O)C2)C3=CC(O)=C(O)C=C3)[C@H]4[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O4
Synonyms:- (-)-(2R,3R)-Dihydroquercetin 3-O-α-<span class="text-smallcaps">L</span>-rhamnoside
- (2R,3R)-3-[(6-Deoxy-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one
- (2R,3R)-Astilbin
- (2R,3R)-Dihydroquercetin 3-O-α-<span class="text-smallcaps">L</span>-rhamnopyranoside
- (2R-trans)-3-((6-Deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one
- 4H-1-Benzopyran-4-one, 3-((6-deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2R,3R)-
- 4H-1-Benzopyran-4-one, 3-((6-deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2R-trans)-
- 4H-1-Benzopyran-4-one, 3-[(6-deoxy-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2R,3R)-
- 4H-1-Benzopyran-4-one, 3-[(6-deoxy-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2R-trans)-
- Astilbin
- Dihydroquercetin 3-O-α-<span class="text-smallcaps">L</span>-rhamnopyranoside
- See more synonyms
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Found 9 products.
Astilbin
CAS:Formula:C21H22O11Purity:≥ 98.0%Color and Shape:White to off-white powderMolecular weight:450.39Astilbin
CAS:Natural glycosideFormula:C21H22O11Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:450.44H-1-Benzopyran-4-one,3-[(6-deoxy-a-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2R,3R)-
CAS:Formula:C21H22O11Purity:97%Color and Shape:SolidMolecular weight:450.39277999999996Taxifolin 3-O-rhamnoside
CAS:Taxifolin 3-O-rhamnoside is a natural flavonoid glycoside, which is primarily sourced from certain plant species, including members of the Pinaceae family. This compound is recognized for its unique chemical structure, comprising taxifolin attached to a rhamnose sugar moiety. Its mode of action predominantly involves the scavenging of free radicals, thanks to its potent antioxidant properties. Taxifolin 3-O-rhamnoside exhibits the ability to neutralize reactive oxygen species, thereby contributing to the protection of cellular components from oxidative stress. In research settings, Taxifolin 3-O-rhamnoside finds applications in studies investigating cellular antioxidative defenses and signaling pathways related to oxidative stress. It serves as a valuable tool for exploring the modulation of oxidative stress responses and offers insights into potential therapeutic strategies for conditions linked to oxidative damage. Furthermore, its role in anti-inflammatory and cardioprotective research underscores its importance in various areas of biochemical and pharmacological studies, paving the way for potential future applications in drug development and phytochemistry.Formula:C21H22O11Purity:Min. 95%Color and Shape:PowderMolecular weight:450.39 g/molAstilbin
CAS:Astilbin (Neoastilbin) is actions Flavonoid phytochemical found in St. John′s wort and Traditional Chinese Medicine herbal preparations.Formula:C21H22O11Purity:97% - 99.76%Color and Shape:White PowderMolecular weight:450.39Ref: TM-T2794
5mg52.00€10mg77.00€25mg140.00€50mg224.00€100mg334.00€200mg477.00€500mg778.00€1mL*10mM (DMSO)51.00€Astilbin
CAS:Astilbin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C21H22O11Purity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:450.4Astilbin
CAS:Astilbin has insecticidal, antioxidant, antibacterial, and anti-inflammatory activities, it may act as an efficient therapeutic agent for arthritis like cyclosporine A but with less toxicity, its mechanism includes a selective suppression on lymphocyte functions via reducing MMP and NO production. Astilbin can exert an early renal protective role to diabetic nephropathy (DN), inhibit production of transforming growth factor-beta1 (TGF-beta1) and connective tissue growth factor (CTGF).Astilbin also alleviates contact hypersensitivity through a unique mechanism involving a negative cytokine regulation through stimulating IL-10, which is distinct from the immunosuppressant cyclosporin A.Formula:C21H22O11Purity:95%~99%Molecular weight:450.396
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