CAS 23313-21-5
:Emodina 8-O-β-D-glucopiranósido
Descripción:
Emodina 8-O-β-D-glucopiranósido es un derivado glicosilado de la emodina, un compuesto de antraquinona que se encuentra de forma natural. Esta sustancia se caracteriza por su estructura molecular, que incluye un moiety de glucopiranósido unido al núcleo de emodina, mejorando su solubilidad y biodisponibilidad. Típicamente exhibe un color amarillo a naranja en su forma pura y es soluble en solventes polares como agua y metanol. Emodina 8-O-β-D-glucopiranósido es conocido por sus potenciales propiedades farmacológicas, incluyendo actividades antiinflamatorias, antioxidantes y anticancerígenas, lo que lo hace de interés en la química medicinal y la investigación de productos naturales. Su presencia en varias plantas, particularmente aquellas utilizadas en la medicina tradicional, resalta su importancia en los remedios herbales. Las actividades biológicas del compuesto se atribuyen a su capacidad para modular diversas vías de señalización, aunque se necesitan más estudios para elucidar completamente sus mecanismos de acción y potencial terapéutico. Al igual que con muchos compuestos naturales, los efectos específicos pueden variar según la concentración, formulación y el contexto biológico en el que se estudia.
Fórmula:C21H20O10
InChI:InChI=1S/C21H20O10/c1-7-2-9-14(11(24)3-7)18(27)15-10(16(9)25)4-8(23)5-12(15)30-21-20(29)19(28)17(26)13(6-22)31-21/h2-5,13,17,19-24,26,28-29H,6H2,1H3/t13-,17-,19+,20-,21-/m1/s1
Clave InChI:InChIKey=HSWIRQIYASIOBE-JNHRPPPUSA-N
SMILES:O(C1=C2C(C(=O)C=3C(C2=O)=C(O)C=C(C)C3)=CC(O)=C1)[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O
Sinónimos:- 1,6-Dihydroxy-3-Methyl-8-(Β-D-Glucopyranosyloxy)-9,10-Anthraquinone
- 1-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-3,8-dihydroxy-6-methyl-9,10-anthracenedione
- 8-O-β-<span class="text-smallcaps">D</span>-Glucopyranosylemodin
- 9,10-Anthracenedione, 1-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-3,8-dihydroxy-6-methyl-
- Anthraglycoside B
- Emodin 8-O-glucoside
- Emodin 8-O-β-<span class="text-smallcaps">D</span>-glucopyranoside
- Emodin 8-O-β-<span class="text-smallcaps">D</span>-glucoside
- Emodin 8-O-β-glucoside
- Emodin 8-β-<span class="text-smallcaps">D</span>-glucopyranoside
- Emodin 8-β-<span class="text-smallcaps">D</span>-glucoside
- Emodin glucoside B
- Glucopyranoside, 3,8-dihydroxy-6-methyl-1-anthraquinonyl, β-<span class="text-smallcaps">D</span>-
- NSC 257449
- Glucopyranoside, 3,8-dihydroxy-6-methyl-1-anthraquinonyl, β-D-
- Emodin 8-β-D-glucoside
- 1-(β-D-Glucopyranosyloxy)-3,8-dihydroxy-6-methyl-9,10-anthracenedione
- Ver más sinónimos
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Encontrado 10 productos.
9,10-Anthracenedione, 1-(β-D-glucopyranosyloxy)-3,8-dihydroxy-6-methyl-
CAS:Fórmula:C21H20O10Pureza:98%Forma y color:SolidPeso molecular:432.3775Emodin-8-glucoside
CAS:Fórmula:C21H20O10Pureza:(HPLC) ≥ 97.0%Forma y color:Orange powderPeso molecular:432.38Emodin-8-glucoside
CAS:Emodin-8-O-beta-D-glucoside extracted from the traditional Chinese medicinal herb Polygonum cuspidatum Sieb. et Zucc is widely used to treat acute hepatitis possibly by antioxidative mechanisms; it is able to provide neuroprotection against cerebral ischemia-reperfused injury and glutamate induced neuronal damage through exerting antioxidative effects and inhibiting glutamate neurotoxicity.Fórmula:C21H20O10Pureza:95%~99%Forma y color:Yellow powderPeso molecular:432.381Emodin-8-glucoside
CAS:Emodin-8-glucoside shields against ischemic brain injury and boosts osteoblast growth.Fórmula:C21H20O10Pureza:97.81%Forma y color:SolidPeso molecular:432.38Emodin 8-β-D-Glucoside
CAS:Producto controlado<p>Applications A glucoside metabolite of Emodin (E523000).<br>References Pan, X., et al.: Biochem. Eng. J., 5, 173 (2000), Srinivas, G., et al.: Eur. J. Pharmacol., 473, 117 (2003), Xiang, H., et al.: Chin. Pharm. J., 40, 96 (2005), Mokhtarani, B., et al.: Biochem. Eng. J., 38, 241 (2008),<br></p>Fórmula:C21H20O10Forma y color:NeatPeso molecular:432.38Emodin 8-O-b-D-glucopyranoside
CAS:<p>Emodin is a natural product that can be extracted from the rhizome of Curcuma aromatica, a chinese herb. It has been shown to have neuroprotective effects in animal studies and has been used as an adjuvant in the treatment of cervical cancer. Emodin also inhibits the replication of human immunodeficiency virus type 1 (HIV-1) and herpes simplex virus type 1 (HSV-1). Emodin is also active against microbial infection, including bacterial infections, such as those caused by Staphylococcus aureus, and viral infections, such as influenza A virus. The main mechanism of action of emodin is its inhibition of DNA synthesis by binding to viral dna or bacterial rna polymerase. Emodin has also been found to inhibit protein synthesis by binding to ribosomes. This drug binds to urea nitrogen molecules in bacteria and disrupts their growth by inhibiting protein synthesis.</p>Fórmula:C21H20O10Pureza:Min. 95%Forma y color:PowderPeso molecular:432.38 g/mol








