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20(S)-Protopanaxatriol CAS: 34080-08-5

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20(S)-Protopanaxatriol CAS: 34080-08-5

20(S)-Protopanaxatriol CAS: 34080-08-5

20(S)-Protopanaxatriol (PPT) is a high-purity aglycone metabolite derived from ginsenosides, isolated from Panax ginseng roots. As a key reference standard, it enables advanced research in oncology, neuroprotection, and metabolic regulation. With ≥98% HPLC-verified purity and batch-specific CoA, this compound meets pharmacopeial requirements for drug development and quality control.

  • Product Name :

    20(S)-Protopanaxatriol
  • CAS No. :

    34080-08-5
  • Appearance :

    White to off-white crystalline powder
  • Specification :

    40%-98%

? 20(S)-Protopanaxatriol (PPT) | CAS: 34080-08-5

Molecular Formula: C??H??O? | Molecular Weight: 476.73
Appearance: White crystalline powder (colorless needles in methanol) | Melting Point: 261–263°C (20S-isomer)
Source: Roots of Panax ginseng 


? Core Value Proposition

? Precision-Grade Purity & Multi-Target Bioactivity

  • Flexible Purity (40%–98%): Rigorously optimized for diverse applications:

    • ≥98% (HPLC-ELSD): For drug development & cellular assays (lot-specific COA with NMR/MS data) 1310

    • 70%–90%: Cost-effective for cosmetics/nutraceutical formulations

    • 40%–60%: Bulk industrial extracts for preliminary screening

  • Bioactivity Validated: Confirmed dual modulation of glucocorticoid receptor (GR) and estrogen receptor (ERβ), with LXRα inhibition (IC??: 482 nM for Ca²? flux in HUVECs) 

? Clinically Relevant Benefits

  • Neuroprotection: Reduces cerebral infarction area by 58% in MCAO stroke models and alleviates brain edema

  • Anti-Tumor Adjuvant: Induces dendritic cell maturation for tumor-specific cytotoxicity and suppresses metastasis via integrin β1/FAK pathway 

  • Metabolic Regulation: Inhibits LXRα-driven lipogenesis (↓ SREBP-1c, ↓ triglyceride accumulation in hepatocytes) 


?? Technical Specifications

Parameter Specification
Purity Grades 40%/70%/90%/98% (HPLC-ELSD, custom options)
Isomer Ratio 20(S):20(R) ≥99:1 (Chiral HPLC-C18) 10
Identification NMR (1H/13C), HRMS, Optical Rotation: +20.5° 
Solubility DMSO (50 mg/mL), ethanol; insoluble in water
Storage 2–8°C, sealed under N?, protected from light
Shelf Life 24 months (stability-validated) 


? Industry Applications

? Neuropharmacology & Stroke Therapy

  • Ischemic Stroke Recovery: Improves motor function in MCAO rats by 45% via BDNF/TrkB pathway activation 

  • Anti-Depressant Effects: Modulates hippocampal GABA? receptors (↓ corticosterone by 52% in chronic stress models)

? Oncology & Immunology

  • Dendritic Cell Activation: Synergizes with antigens to enhance tumor-specific CTL responses 

  • Chemo-Adjuvant: Reverses P-gp-mediated drug resistance in leukemia (K562/ADR cell line) 

? Cosmetic & Nutraceuticals

  • Skin Barrier Repair: Upregulates ceramide synthesis for anti-aging formulations (70% purity grade)

  • Metabolic Health: Controls lipid accumulation in obesity models (LXRα-dependent pathway) 


? Competitive Edge

Advantage Impact
Purity Flexibility Tailored cost/performance ratios for R&D vs. bulk use
Sustainable Sourcing Traceable to cultivated Panax ginseng (DNA-barcoded) 
Analytical Rigor Lot-specific activity reports (GR/ER binding assays included)
Global Compliance ISO 9001/Kosher, heavy metals ≤5 ppm (USP/EP) 

? Packaging & Delivery

Purity Grade Primary Packaging Quantity Range Shipping Protocol
≥98% Amber glass vials 20mg–100mg Dry ice (-78°C), 3–7 days
70%–90% Pharma-grade PET bottles 100mg–10kg Cold chain (2–8°C), 5–10 days
40%–60% GMP-compliant drums 10kg–100kg Sea freight (-20°C monitored), 15–45 days


? FAQ

Q: How to select purity grade for neuroprotective studies?
→ Free 20mg samples (98% grade) provided with stroke model efficacy data (e.g., MCAO infarction reduction) 

Q: Solubility challenges in topical formulations?
→ Solution: Nano-emulsion kits available (OEM service; ↑ water dispersibility 500-fold)

Q: Stability in cell culture media?
→ Stable for 72h in serum-free buffers (recommend fresh DMSO stock ≤10mM)

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