CAS 72063-39-9
:Spinosin
Description:
Spinosin, with the CAS number 72063-39-9, is a natural compound primarily derived from the plant species *Ziziphus jujuba*, commonly known as jujube. It belongs to the class of flavonoids and is recognized for its potential pharmacological properties. Spinosin is characterized by its unique chemical structure, which includes a flavone backbone, contributing to its bioactivity. This compound has garnered interest in the field of herbal medicine due to its reported anxiolytic, sedative, and neuroprotective effects. Additionally, spinosin exhibits antioxidant properties, which may help in mitigating oxidative stress in biological systems. Its solubility profile suggests it is more soluble in organic solvents than in water, which can influence its bioavailability and therapeutic applications. Research into spinosin continues to explore its mechanisms of action and potential benefits in treating various health conditions, particularly those related to anxiety and sleep disorders. Overall, spinosin represents a significant area of interest in natural product chemistry and pharmacology.
Formula:C28H32O15
InChI:InChI=1S/C28H32O15/c1-39-14-7-15-18(12(32)6-13(40-15)10-2-4-11(31)5-3-10)22(35)19(14)26-27(24(37)21(34)16(8-29)41-26)43-28-25(38)23(36)20(33)17(9-30)42-28/h2-7,16-17,20-21,23-31,33-38H,8-9H2,1H3/t16-,17-,20-,21-,23+,24+,25-,26+,27-,28+/m1/s1
InChI key:InChIKey=VGGSULWDCMWZPO-ODEMIOGVSA-N
SMILES:O(C)C1=C(C(O)=C2C(=C1)OC(=CC2=O)C3=CC=C(O)C=C3)[C@H]4[C@H](O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@@H](CO)O4
Synonyms:- (1S)-1,5-Anhydro-2-O-beta-D-glucopyranosyl-1-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxo-4H-chromen-6-yl]-D-glucitol
- 4H-1-Benzopyran-4-one, 6-(2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-
- 4H-1-Benzopyran-4-one, 6-(2-O-β-<span class="text-smallcaps">D</smallcap>-glucopyranosyl-β-<smallcap>D</span>-glucopyranosyl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-
- 6-(2-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
- 6-(2-O-β-<span class="text-smallcaps">D</smallcap>-Glucopyranosyl-β-<smallcap>D</span>-glucopyranosyl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
- D-glucitol, 1,5-anhydro-2-O-beta-D-glucopyranosyl-1-C-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxo-4H-1-benzopyran-6-yl]-, (1S)-
- Flavoayamenin
- Spinosin
- Swertisin 2′′-O-glucoside
- 6-(2-O-β-D-Glucopyranosyl-β-D-glucopyranosyl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
- 4H-1-Benzopyran-4-one, 6-(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 11 products.
Spinosin
CAS:Other glycosides, natural or reproduced by synthesis, and their salts, ethers, esters and other derivativesFormula:C28H32O15Color and Shape:Yellow PowderMolecular weight:608.55Spinosin
CAS:Spinosin has neuroprotective, anxiolytic-like and anti-inflammatory effects, it ameliorated memory impairment induced through AβO, the serotonergic neurotransmitter system, it also potentiated pentobarbital-induced sleep via the serotonergic system.Formula:C28H32O15Purity:95%~99%Molecular weight:608.549Spinosin
CAS:Formula:C28H32O15Purity:>95.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:608.55Spinosin
CAS:<p>1.</p>Formula:C28H32O15Purity:98.16% - 99.75%Color and Shape:SolidMolecular weight:608.54Spinosin
CAS:Natural glycosideFormula:C28H32O15Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:608.55Spinosin
CAS:Controlled Product<p>Applications Spinosin is a C-glycoside flavonoid extracted from Zizhiphi Spinozae, improved pentobarbital-induced sleep.<br>References Wang, Li. et al.: Pharm. Biochem. Behav., 90, 399 (2008);<br></p>Formula:C28H32O15Color and Shape:NeatMolecular weight:608.54Spinosin
CAS:<p>Spinosin is a natural product that belongs to the group of pyrrolizidine alkaloids. It has been shown to have physiological function as it can inhibit the 5-HT1A receptor and thereby regulate neurotransmitter release. Spinosin also has anti-inflammatory effects and can be used in the treatment of skin disorders, such as psoriasis. In vitro studies have shown that spinosin is a substrate for P-gp and interacts with other drugs by inhibiting their absorption in the gut and liver. Spinosin has been found to bind to monoclonal antibodies, which may be due to its structural similarity to chinese herb, a known antigenic protein. This leads to increased uptake of spinosin into cells and thus makes it an analytical method for measuring spinosin in biological samples. Spinosin activates p38mapk which then causes the phosphorylation of ERK1/2, leading to receptor binding and activation of downstream signaling pathways.</p>Formula:C28H32O15Purity:Min. 95%Color and Shape:PowderMolecular weight:608.54 g/mol










