Structure of Ginsenoside Re
CAS No.: 52286-59-6
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Ginsenoside Re is a panaxatriol saponin that has diverse in vitro and in vivo effects, including vasorelaxant, antioxidant, antihyperlipidemic, and angiogenic actions.
Synonyms: Panaxoside Re; Ginsenoside B2; NSC 308877
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CAS No. : | 52286-59-6 |
Formula : | C48H82O18 |
M.W : | 947.15 |
SMILES Code : | C[C@@]12[C@@]([H])([C@](C)([C@]3([C@H](C2)O[C@@H]([C@@H]4O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)O)O)O)O[C@@H]([C@H]([C@@H]4O)O)CO)[H])CC[C@@H](C3(C)C)O)C[C@H]([C@]6([C@]1(CC[C@@]6([C@@](C)(O[C@@H]7O[C@@H]([C@H]([C@@H]([C@H]7O)O)O)CO)CC/C=C(C)\C)[H])C)[H])O |
Synonyms : |
Panaxoside Re; Ginsenoside B2; NSC 308877
|
MDL No. : | MFCD00133369 |
InChI Key : | PWAOOJDMFUQOKB-WCZZMFLVSA-N |
Pubchem ID : | 441921 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Target |
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In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
SH-SY5Y cells | 25 µM | 24 hours | To evaluate the protective effect of ginsenoside Re against Aβ25-35-induced cytotoxicity and apoptosis, results showed ginsenoside Re significantly increased cell viability and reduced apoptosis. | Molecules. 2019 Jul 24;24(15):2687 |
SH-SY5Y cells | 10–100 µM | 9 h pretreatment followed by 24 h exposure to 6-OHDA | To evaluate the protective effect of ginsenoside Re against 6-OHDA-induced cellular damage. Results showed that ginsenoside Re significantly inhibited 6-OHDA-triggered cellular damage, reduced LDH release, and improved cell viability. | Molecules. 2020 Jan 2;25(1):188 |
Mouse bone marrow-derived macrophages (BMMs) | 0-10 μM | 3 days | To investigate the effect of Ginsenoside Re on RANKL-induced osteoclast differentiation, results showed that Ginsenoside Re inhibited osteoclast differentiation in a dose-dependent manner. | Mol Cells. 2016 Dec;39(12):855-861 |
Mouse osteoblast precursor MC3T3-E1 cells | 50 μM | 21 days | To evaluate the effect of ginsenoside Re on mineralization, results showed significant increase in calcium deposition at 50 μM. | Molecules. 2016 Dec 29;22(1):42 |
Mouse osteoblast precursor MC3T3-E1 cells | 50, 100 μM | 14 days | To evaluate the effect of ginsenoside Re on alkaline phosphatase (ALP) activity, results showed significant promotion of ALP activity at 50-100 μM. | Molecules. 2016 Dec 29;22(1):42 |
Mouse osteoblast precursor MC3T3-E1 cells | 5, 10, 25, 50, 100 μM | 24 hours | To evaluate the effect of ginsenoside Re on cell viability in MC3T3-E1 cells, results showed no cytotoxicity at 100 μM. | Molecules. 2016 Dec 29;22(1):42 |
Cardiac fibroblasts | 50 μmol/L, 100 μmol/L, 200 μmol/L | 24 hours | To investigate the effect of Ginsenoside Re on AngII-induced fibrosis in cardiac fibroblasts. Results showed that Ginsenoside Re could inhibit the expression of collagen I, collagen III, and α-SMA, alleviating fibrosis. | J Ginseng Res. 2023 Mar;47(2):218-227 |
human dermal papilla cells (hDPCs) | 3 μM | 6 hours | To investigate the effect of ginsenoside Re on autophagy, results showed that ginsenoside Re increased LC3-II conversion and Beclin 1 expression, promoting autophagy. | J Ginseng Res. 2023 May;47(3):440-447 |
mouse small intestine interstitial cells of Cajal | 20-40 μM | To investigate the effects of Ginsenoside Re on the pacemaker activity of interstitial cells of Cajal, results showed that Ginsenoside Re decreased the amplitude and frequency of pacemaker activity in a concentration-dependent manner. | J Ginseng Res. 2015 Oct;39(4):314-21 | |
HT22 hippocampal neuronal cells | 2.5, 5.5 or 7.5 µg/ml | 1 hour | Ginsenoside Re protected hippocampal neuronal cells by reducing inflammatory and neurotoxic factors released from microglial cells. | Mol Med Rep. 2021 Oct;24(4):698 |
Mouse primary microglia | 2.5, 5.5 or 7.5 µg/ml | 1 hour | Ginsenoside Re inhibited NO production and the expression of iNOS and COX-2. | Mol Med Rep. 2021 Oct;24(4):698 |
BV2 microglial cells | 2.5, 5.5 or 7.5 µg/ml | 1 hour | Ginsenoside Re significantly inhibited LPS-induced production of IL-6, TNF-α, NO, and ROS, and suppressed the expression of iNOS and COX-2. | Mol Med Rep. 2021 Oct;24(4):698 |
HeLa-mitoKeima-PARKIN cells | 25 and 50 μM | 24 hours | To assess the ability of G-Re to induce mitophagy, results showed that G-Re significantly increased the population of mitophagy-positive cells. | J Ginseng Res. 2025 Jan;49(1):92-102 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Mice | Wild-type mice and prodynorphin knockout mice | Intraperitoneal injection | 20 mg/kg | Twice daily for 7 consecutive days (5 days before and 1 day after MA injection) | Ginsenoside Re protects methamphetamine-induced dopaminergic neurotoxicity via upregulation of dynorphin-mediated κ-opioid receptor and downregulation of substance P-mediated neurokinin 1 receptor. | J Neuroinflammation. 2018 Feb 21;15(1):52 |
Zebrafish | Zebrafish scale model | Water solution | 50 μM | Daily water replacement for 35 days | To evaluate the effect of ginsenoside Re on zebrafish scale mineralization, results showed significant increase in calcium deposition at 50 μM. | Molecules. 2016 Dec 29;22(1):42 |
C57BL/6 mice | Acute myocardial infarction model | Intragastric administration | 19.5 mg/kg/d, 39 mg/kg/d | Once daily for 4 weeks | To investigate the effect of Ginsenoside Re on myocardial fibrosis in mice with acute myocardial infarction. Results showed that Ginsenoside Re could improve cardiac function, inhibit collagen deposition and cardiac fibroblast migration, promote miR-489 transcription, and reduce myd88 expression and NF-κB p65 phosphorylation. | J Ginseng Res. 2023 Mar;47(2):218-227 |
Caenorhabditis elegans | Wild-type N2 Caenorhabditis elegans and specific mutants | Oral | 10, 20, and 50 μM | Continuous administration | To evaluate the effects of G-Re on lifespan and health metrics, results showed that G-Re extended lifespan and improved health metrics such as movement speed and stress resistance. | J Ginseng Res. 2025 Jan;49(1):92-102 |
Balb/c mice | Cyclophosphamide-induced myelosuppression model | Intraperitoneal injection | 5 and 10 mg/kg | Once a day for 7 consecutive days | To investigate the effects of Ginsenoside Re on cyclophosphamide-induced myelosuppression, results showed that Re improved peripheral blood cell counts, bone marrow nucleated cell counts, thymus index, and spleen index, and regulated cytokine levels and cell cycle. | J Ginseng Res. 2019 Oct;43(4):618-624 |
Zebrafish | Zebrafish scale model | Water administration | 5 μM | Once daily for 35 days | To evaluate the inhibitory effect of Ginsenoside Re on osteoclast differentiation in zebrafish scales, results showed that Ginsenoside Re significantly reduced TRAP-positive signals and the expression of osteoclast marker genes. | Mol Cells. 2016 Dec;39(12):855-861 |
Tags: Ginsenoside Re | Ginsenoside B2 | Panaxoside Re | Sanchinoside Re | Amyloid-β | NF-κB | JNK | Endogenous Metabolite | β-amyloid peptide | Abeta | Nuclear factor-κB | Nuclear factor-kappaB | c-Jun N-terminal kinase | inhibitor | 52286-59-6 |
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