CAS 52286-59-6: Ginsenósido Re
Descripción:
Ginsenósido Re es un compuesto natural clasificado como una saponina triterpenoide, que se encuentra principalmente en especies de ginseng, particularmente en Panax ginseng. Se conoce por su estructura compleja, que incluye un esqueleto similar a un esteroide con múltiples moieties de azúcar adjuntas, lo que contribuye a su bioactividad. Ginsenósido Re exhibe diversas propiedades farmacológicas, incluyendo efectos antiinflamatorios, antioxidantes y neuroprotectores, lo que lo convierte en un tema de interés en química medicinal y farmacología. Su mecanismo de acción a menudo implica la modulación de vías de señalización, influyendo en procesos celulares como la apoptosis y la proliferación. Además, se ha estudiado Ginsenósido Re por sus posibles beneficios en la mejora de la función cognitiva y el apoyo a la salud cardiovascular. El compuesto se extrae típicamente de las raíces de ginseng y se puede analizar utilizando técnicas como la cromatografía líquida de alta resolución (HPLC). Debido a su potencial terapéutico, Ginsenósido Re a menudo se incluye en suplementos dietéticos y formulaciones herbales destinadas a promover la salud y el bienestar en general. Sin embargo, se necesita más investigación para elucidar completamente sus mecanismos y aplicaciones terapéuticas.
Fórmula:C48H82O18
InChI:InChI=1S/C48H82O18/c1-21(2)11-10-14-48(9,66-42-38(60)35(57)32(54)26(19-49)63-42)23-12-16-46(7)30(23)24(51)17-28-45(6)15-13-29(52)44(4,5)40(45)25(18-47(28,46)8)62-43-39(36(58)33(55)27(20-50)64-43)65-41-37(59)34(56)31(53)22(3)61-41/h11,22-43,49-60H,10,12-20H2,1-9H3/t22-,23-,24+,25-,26+,27+,28+,29-,30-,31-,32+,33+,34+,35-,36-,37+,38+,39+,40-,41-,42-,43+,45+,46+,47+,48-/m0/s1
Clave InChI:InChIKey=PWAOOJDMFUQOKB-WCZZMFLVSA-N
SMILES:C[C@]12[C@@]([C@]3(C)[C@@]([C@@H](O[C@H]4[C@H](O[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)[C@@H](O)[C@H](O)[C@@H](CO)O4)C1)(C(C)(C)[C@@H](O)CC3)[H])(C[C@@H](O)[C@]6([C@@]2(C)CC[C@@]6([C@@](O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)(CCC=C(C)C)C)[H])[H])[H]
Sinónimos:- (3β,6α,12β)-20-(β-<span class="text-smallcaps">D</smallcap>-Glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl)-β-<smallcap>D</span>-glucopyranoside
- 2-O-(6-Desoxy-α-L-mannopyranosyl)-(3β,6α,12β)-20-(β-D-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl-β-D-glucopyranosid
- 2-O-(6-deoxy-α-L-mannopyranosyl)-(3β,6α,12β)-20-(β-D-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl-β-D-glucopyranoside
- 2-O-(6-desoxi-α-L-manopiranosil)-(3β,6α,12β)-20-(β-D-glucopiranosiloxi)-3,12-dihidroxidamar-24-en-6-il-β-D-glucopiranosido
- 2-O-(6-desoxy-α-L-mannopyrannosyl)-(3β,6α,12β)-20-(β-D-glucopyrannosyloxy)-3,12-dihydroxydammar-24-ene-6-yl-β-D-glucopyrannoside
- Chikusetsusaponin IVc
- Ginsenoside B2
- Ginsenoside B<sub>2</sub>
- Ginsenoside Re
- Notoginsenoside Re
- Nsc 308877
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Encontrado 11 productos.
Ginsenoside Re
CAS:Fórmula:C48H82O18Pureza:>95.0%(HPLC)(qNMR)Forma y color:White to Light yellow powder to crystalPeso molecular:947.17Ginsenoside Re
CAS:Ginsenoside Re, a main phytosterol of Panax ginseng, inhibits Ca(2+) accumulation in mitochondria during cardiac ischemia/reperfusion, which is attributable to nitric oxide (NO)-induced Ca(2+) channel inhibition and K(+) channel activation in cardiac myocytes, acts as a specific agonist for the nongenomic pathway of sex steroid receptors, and NO released from activated eNOS underlies cardiac K(+) channel activation and protection against ischemia-reperfusion injury, G-Re also exerts antiischemic effect and induces angiogenic regeneration.[1,2]Fórmula:C48H82O18Pureza:95%~99%Forma y color:White powderPeso molecular:947.166Ginsenoside Re
CAS:Ginsenoside Re is a naturally occurring saponin, which is a bioactive compound sourced primarily from the root of Panax ginseng. It operates through multiple biochemical pathways, including the modulation of immune responses, anti-inflammatory effects, and protective antioxidant activities. Ginsenoside Re exerts its actions by interacting with cellular receptors, influencing signaling pathways such as the PI3K/Akt and MAPK pathways, ultimately impacting gene expression and cellular responses. The compound is extensively utilized in pharmacological research for its potential therapeutic benefits. It is investigated for roles in enhancing cognitive function, promoting cardiovascular health, and mitigating oxidative stress-related damage. Ginsenoside Re is also studied for its possible antidiabetic properties and as a supportive agent in cancer therapy. Its diverse biological activities make it a significant subject of interest in the development of novel therapeutic agents targeting a range of health conditions.Fórmula:C48H82O18Pureza:Min. 98 Area-%Forma y color:White PowderPeso molecular:947.18 g/molGinsenoside Re
CAS:Applications Ginsenoside Re is an extract from ginger, responsible for some of the pharmacological functions. It displays cardiac contractility, anti-ischemic and anti-arrythmic activities. References Peng, D. et al.: Chinese Med., 7, 2 (2012); Endale, M. et al.: Med. Inflamm., 748964/1 (2014);Fórmula:C48H82O18Forma y color:NeatPeso molecular:947.15Ginsenoside Re
CAS:Fórmula:C48H82O18Pureza:≥ 98.0%Forma y color:White to off-white powderPeso molecular:947.15Ginsenoside Re
CAS:Ginsenoside Re analytical standard provided with w/w absolute assay, to be used for quantitative titration.Fórmula:C48H82O18Pureza:(HPLC) ≥98%Forma y color:PowderPeso molecular:947.18Ginsenoside re
CAS:Natural glycosideFórmula:C48H82O18Pureza:≥ 95.0 % (HPLC)Forma y color:PowderPeso molecular:947.17Ginsenoside Re
CAS:Ginsenoside Re (Ginsenoside B2) may have properties that inhibit or prevent the growth of tumors.Fórmula:C48H82O18Pureza:100% - 99.78%Forma y color:White PowderPeso molecular:947.15
