CAS 52286-59-6
:Ginsenoside Re
Descrizione:
Ginsenoside Re è un composto naturale classificato come saponina triterpenoide, trovato principalmente nelle specie di ginseng, in particolare nel Panax ginseng. È noto per la sua struttura complessa, che include uno scheletro simile a uno steroide con più moieties di zucchero attaccati, contribuendo alla sua bioattività. Ginsenoside Re mostra varie proprietà farmacologiche, inclusi effetti anti-infiammatori, antiossidanti e neuroprotettivi, rendendolo un argomento di interesse in chimica medicinale e farmacologia. Il suo meccanismo d'azione spesso implica la modulazione delle vie di segnalazione, influenzando processi cellulari come apoptosi e proliferazione. Inoltre, Ginsenoside Re è stato studiato per i suoi potenziali benefici nel migliorare la funzione cognitiva e nel supportare la salute cardiovascolare. Il composto viene tipicamente estratto dalle radici di ginseng e può essere analizzato utilizzando tecniche come la cromatografia liquida ad alte prestazioni (HPLC). A causa del suo potenziale terapeutico, Ginsenoside Re è spesso incluso in integratori alimentari e formulazioni a base di erbe destinate a promuovere la salute e il benessere generale. Tuttavia, sono necessarie ulteriori ricerche per chiarire completamente i suoi meccanismi e le sue applicazioni terapeutiche.
Formula: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
InChI key: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]
Sinonimi:- (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
- Panaxoside Re
- Re ginsenoside
- Sanchinoside Re
- β-<span class="text-smallcaps">D</smallcap>-Glucopyranoside, (3β,6α,12β)-20-(β-<smallcap>D</smallcap>-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-<smallcap>L</span>-mannopyranosyl)-
- 2-O-(6-Deoxy-alpha-L-mannopyranosyl)-(3beta,6alpha,12beta)-20-(beta-D-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl-beta-D-glucopyranoside
- (3β,6α,12β)-20-(β-D-Glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
- (3beta,6alpha,12beta)-20-(beta-D-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside
- Ginsenoside
- β-D-Glucopyranoside, (3β,6α,12β)-20-(β-D-glucopyranosyloxy)-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-
- (3beta,6alpha,9xi,12beta,13alpha)-20-[(3xi)-beta-D-ribo-hexopyranosyloxy]-3,12-dihydroxydammar-24-en-6-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside
- Vedi altri sinonimi
Ordinare per
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11 prodotti.
Ginsenoside Re
CAS:Ginsenoside Re analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C48H82O18Purezza:(HPLC) ≥98%Colore e forma:PowderPeso molecolare:947.18Ginsenoside 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]Formula:C48H82O18Purezza:95%~99%Colore e forma:White powderPeso molecolare:947.166Ginsenoside Re
CAS:Formula:C48H82O18Purezza:>95.0%(HPLC)(qNMR)Colore e forma:White to Light yellow powder to crystalPeso molecolare:947.17Ginsenoside Re
CAS:Ginsenoside Re (Ginsenoside B2) may have properties that inhibit or prevent the growth of tumors.Formula:C48H82O18Purezza:99.12% - >99.99%Colore e forma:White PowderPeso molecolare:947.15Ginsenoside Re
CAS:Formula:C48H82O18Purezza:≥ 98.0%Colore e forma:White to off-white powderPeso molecolare:947.15Ginsenoside re
CAS:Natural glycosideFormula:C48H82O18Purezza:≥ 95.0 % (HPLC)Colore e forma:PowderPeso molecolare:947.17Ginsenoside Re
CAS:<p>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.<br>References Peng, D. et al.: Chinese Med., 7, 2 (2012); Endale, M. et al.: Med. Inflamm., 748964/1 (2014);<br></p>Formula:C48H82O18Colore e forma:NeatPeso molecolare:947.15Ginsenoside Re
CAS:<p>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.</p>Formula:C48H82O18Purezza:Min. 98 Area-%Colore e forma:White PowderPeso molecolare:947.18 g/molRef: ST-EA-CP-G62008
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