CAS 72063-39-9
:Espinosina
Descripción:
Espinosina, con el número CAS 72063-39-9, es un compuesto natural derivado principalmente de la especie vegetal *Ziziphus jujuba*, comúnmente conocida como jujube. Pertenece a la clase de los flavonoides y se reconoce por sus potenciales propiedades farmacológicas. Espinosina se caracteriza por su estructura química única, que incluye un esqueleto de flavona, contribuyendo a su bioactividad. Este compuesto ha despertado interés en el campo de la medicina herbal debido a sus efectos ansiolíticos, sedantes y neuroprotectores reportados. Además, Espinosina exhibe propiedades antioxidantes, que pueden ayudar a mitigar el estrés oxidativo en sistemas biológicos. Su perfil de solubilidad sugiere que es más soluble en disolventes orgánicos que en agua, lo que puede influir en su biodisponibilidad y aplicaciones terapéuticas. La investigación sobre Espinosina continúa explorando sus mecanismos de acción y beneficios potenciales en el tratamiento de diversas condiciones de salud, particularmente aquellas relacionadas con la ansiedad y los trastornos del sueño. En general, Espinosina representa un área significativa de interés en la química de productos naturales y la farmacología.
Fórmula: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
Clave InChI: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
Sinónimos:- (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-
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Encontrado 11 productos.
Spinosin
CAS:Other glycosides, natural or reproduced by synthesis, and their salts, ethers, esters and other derivativesFórmula:C28H32O15Forma y color:Yellow PowderPeso molecular:608.17412Spinosin
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.Fórmula:C28H32O15Pureza:95%~99%Peso molecular:608.549Spinosin
CAS:Fórmula:C28H32O15Pureza:>95.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:608.55Spinosin
CAS:Natural glycosideFórmula:C28H32O15Pureza:≥ 90.0 % (HPLC)Forma y color:PowderPeso molecular:608.55Spinosin
CAS:Producto controlado<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>Fórmula:C28H32O15Forma y color:NeatPeso molecular: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>Fórmula:C28H32O15Pureza:Min. 95%Forma y color:PowderPeso molecular:608.54 g/mol










