Pseudoginsenoside RT4
Based on 1 Customer Validation
Pseudoginsenoside RT4 is an orally active anti-inflammatory agent. Pseudoginsenoside RT4 can be isolated from Panax pseudoginseng subsp. Himalaicus, Panax vietnamensis Ha et Grushv, and Panax quinquefolius L. Pseudoginsenoside RT4 reduces the levels of TNF-α, IL-6, and IL-1β, elevates the level of IL-10, improves the histopathological features of colon tissue, maintains the ultrastructure of colonic epithelium, protects the integrity of cell monolayers, increases the expression of tight junction proteins, raises the total content of short-chain fatty acids, corrects intestinal flora disorder, reduces the disease activity index score, restores colon length, and decreases the spleen index. Pseudoginsenoside RT4 exhibits hepatoprotective effects. Pseudoginsenoside RT4 can be used in studies related to ulcerative colitis.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 97.05%
- CAS 番号: 98474-77-2
- 分子式: C36H62O10
- 分子量:654.87
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保管条件:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
生物活性
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IL-6 |
IL-1β |
IL-10 |
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| Hepatocyte | IC50 |
74.8 μM
Compound: 4
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Hepatoprotective activity in mouse hepatocytes assessed inhibition of D-galactosamine/TNFalpha-induced cell death dosed administered before 30 mins of TNFalpha challenge measured after 18 hrs
Hepatoprotective activity in mouse hepatocytes assessed inhibition of D-galactosamine/TNFalpha-induced cell death dosed administered before 30 mins of TNFalpha challenge measured after 18 hrs
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[PMID: 11325227] |
Pseudoginsenoside RT4 (4-16 µg/mL; 18 h) protects LPS-induced Caco-2 cell epithelial barrier damage by down-regulating pro-inflammatory cytokines, increasing TEER values, and enhancing tight-junction protein expression, with the strongest effects seen at 16 µg/mL[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:Caco-2
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Concentration:4-16 µg/mL (anti-inflammatory/barrier protection assay); 0-64 µg/mL (cell viability assay)
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Incubation Time:18 h (anti-inflammatory/barrier protection assay); 4 h (cell viability assay)
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Result:Maintained cell viability above 80% at 4, 8, and 16 µg/mL.
Dose-dependently down-regulated levels of pro-inflammatory factors TNF-α, IL-6, and IL-1β.
Significantly reduced all three pro-inflammatory factors at 8 and 16 µg/mL.
Specifically reduced IL-6 levels at 4 µg/mL.
Increased TEER values compared to the LPS-induced model group at 16 µg/mL.
Dose-dependently increased the expression and restored the membrane distribution of tight-junction proteins ZO-1, occludin, claudin-1, and E-cadherin at 4, 8, and 16 µg/mL.
| Species | Dose | Route | AUC0-t | AUC0-∞ | T1/2 | Tmax | Vd | CL | Cmax | Bioavailability |
|---|---|---|---|---|---|---|---|---|---|---|
| Mice[1] | 10 mg/kg | i.g. | 991.55 h·μg/L | 1139.92 h·μg/L | 4.67 h | 1.50 h | 61.91 L/kg | 9.12 L/h/kg | 165.13 μg/L | / |
| Mice[1] | 20 mg/kg | i.g. | 2438.90 h·μg/L | 2698.59 h·μg/L | 6.29 h | 1.17 h | 71.24 L/kg | 8.04 L/h/kg | 295.59 μg/L | / |
| Mice[1] | 40 mg/kg | i.g. | 5288.20 h·μg/L | 5993.63 h·μg/L | 7.17 h | 1.33 h | 71.60 L/kg | 7.20 L/h/kg | 658.65 μg/L | 18.90 % |
| Mice[1] | 2 mg/kg | i.v. | 1246.37 h·μg/L | 1380.43 h·μg/L | 2.24 h | 0.03 h | 4.57 L/kg | 1.51 L/h/kg | 1970.34 μg/L | / |
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Balb/c (male, 6-7-week-old, DSS-induced ulcerative colitis)[1]
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Dosage:10 mg/kg; 20 mg/kg; 40 mg/kg
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Administration:i.g.; daily; 3 days
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Result:Reduced disease activity index (DAI) scores at 20 mg/kg and 40 mg/kg doses.
Increased body weight compared to the model group at 40 mg/kg dose.
Lengthened colon length at 20 mg/kg and 40 mg/kg doses; showed no statistically significant effect on colon length at 10 mg/kg dose.
Lowered spleen index in a dose-dependent manner across all three doses.
Decreased levels of pro-inflammatory cytokines TNF-α, IL-6, and IL-1β in serum and colon, and increased levels of anti-inflammatory cytokine IL-10 in serum and colon at 40 mg/kg dose.
Decreased levels of TNF-α, IL-6, and IL-1β in serum and colon, and increased colon IL-10 levels at 20 mg/kg dose.
Decreased levels of TNF-α, IL-6, and IL-1β in colon tissue at 10 mg/kg dose.
Restored total short-chain fatty acid (SCFA) content in cecal contents toward normal levels across all three doses.
Improved colonic histopathology in a dose-dependent manner: partially restored colonic crypt structure and reduced inflammatory infiltration at 10 mg/kg dose; clearly restored crypt structure and quantity and reduced inflammation at 20 mg/kg dose; restored crypt structure and quantity to near-normal levels with minimal inflammatory cell infiltration at 40 mg/kg dose.
Restored the ultrastructure of colonic mucosal epithelial cells in a dose-dependent manner, with 40 mg/kg dose maintaining near-normal microvilli arrangement and no organelle degeneration.
Increased gut microbiota operational taxonomic unit (OTU) count from 4677 (model group) to 7228, restored Shannon index to near-normal levels, and shifted gut microbiota structure toward that of normal mice at 40 mg/kg dose.
Normalized phylum-level abundances (reduced Acidobacteria, Proteobacteria, Epsilonbacteraeota, Actinobacteria; increased Tenericutes, Bacteroidetes) and genus-level abundances (reduced Escherichia-Shigella, Bacteroides; increased Alloprevotella, Rikenellaceae RC9 gut group, Odoribacter, Alistipes, Lactobacillus) at 40 mg/kg dose.
化学情報
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CAS 番号 98474-77-2
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性状 Solid
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分子量 654.87
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分子式 C36H62O10
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Color White to off-white
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SMILES
C[C@]12[C@]3([C@@]([C@@H](C[C@]1([H])[C@@]4([C@@](C(C)([C@H](CC4)O)C)([H])[C@H](C2)O[C@@H]5O[C@@H]([C@H]([C@@H]([C@H]5O)O)O)CO)C)O)([H])[C@]([C@]6(O[C@@H](CC6)C(C)(O)C)C)([H])CC3)C
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Structure Classification
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Initial Source
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
純度とドキュメンテーション
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データシート (296 KB)
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SDS (252 KB)
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- Français - FR (252 KB)
- Deutsch - DE (252 KB)
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- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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取扱説明書 (2659 KB)
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
Pseudoginsenoside RT4 関連分類
HY-N17685 関連分類
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