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High-Purity Triptolide 98% | CAS 38748-32-2 | Sourced from Tripterygium wilfordii

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High-Purity Triptolide 98% | CAS 38748-32-2 | Sourced from Tripterygium wilfordii

High-Purity Triptolide 98% | CAS 38748-32-2 | Sourced from Tripterygium wilfordii

Triptolide 98% (CAS: 38748-32-2) is a bioactive diterpenoid epoxide derived from the roots and stems of the medicinal plant Tripterygium wilfordii (Thunder God Vine). This high-purity compound is a potent inhibitor of NF-κB activation, making it invaluable for pharmaceutical research, oncology studies, and anti-inflammatory drug development.

  • Product Name :

    Triptolide
  • CAS No. :

    38748-32-2
  • Appearance :

    White crystalline powder
  • Specification :

    98%

??Triptolide 98% (CAS: 38748-32-2)

Plant Source: Tripterygium wilfordii Hook. f. (Thunder God Vine)
Molecular Formula: C??H??O? | Molecular Weight: 360.4 g/mol
Purity: ≥98% (HPLC-validated)
Appearance: White crystalline powder


?? Chemical & Physical Properties

Property Value
Melting Point 226-227°C 
Boiling Point 601.7±55.0°C (760 mmHg) 
Density 1.48±0.1 g/cm³ 24
Solubility Soluble in DMSO (33 mg/mL), methanol, chloroform; insoluble in water 
Storage 2-8°C, sealed, dry, and protected from light 

?? Product Specifications

  • CAS No.: 38748-32-2

  • Synonyms: PG490, Tripdiolide, Triptolide

  • Purity: ≥98% (HPLC, UV detection at 215-218 nm) 

  • Packaging: 5 mg, 20 mg, 50 mg, 100 mg, 500 mg, 1 g (customizable) 

  • Stability: Stable under recommended storage; avoid repeated freeze-thaw cycles 

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?? Biological Activities & Mechanisms

?? In Vitro & In Vivo Efficacy

  1. Anti-Cancer Activity:

    • Induces apoptosis in tumor cells by inhibiting c-IAP2/XIAP and enhancing TNF-α-induced cell death.

    • Targets HSF1-HSP90 complex, suppressing cancer cell proliferation (IC??: 47-73 nM).

    • Inhibits neuroblastoma colony formation and tumorigenicity in xenograft models.

  2. Anti-Inflammatory & Immunosuppressive Effects:

    • Blocks NF-κB activation and TGF-β1/Smad signaling, reducing airway smooth muscle proliferation in asthma models.

    • Synergizes with cyclosporine A to suppress graft-versus-host disease (GVHD) .

  3. Antiviral Action:

    • Downregulates Epstein-Barr virus (EBV) LMP1 protein, inhibiting B-lymphocyte proliferation.

  4. Osteolysis Inhibition:

    • Suppresses RANKL-induced osteoclast formation and titanium particle-induced bone resorption in murine models.


?? Clinical & Research Applications

  • Oncology: Potential therapeutic agent for neuroblastoma, leukemia, and solid tumors.

  • Autoimmune Diseases: Validated for rheumatoid arthritis and asthma via TGF-β/Smad pathway inhibition.

  • Organ Transplantation: Enhances allogeneic bone marrow transplant survival.


?? Experimental Protocols

  1. Cell-Based Assays:

    • Use in DMSO at working concentrations (e.g., 10–100 nM for apoptosis studies).

    • Centrifuge vials before use to prevent compound adhesion.

  2. Animal Studies:

    • Dose-dependent suppression of tumor growth (e.g., 0.1–0.3 mg/kg in mice).


?? Safety & Handling

  • Toxicity: High acute toxicity (LD?? in mice: 0.8–0.9 mg/kg, intraperitoneal).

  • Precautions:

    • Use personal protective equipment (gloves, N95 mask, eyeshields).

    • Avoid contact with strong acids/bases 7.

  • Regulatory: For research use only. Not for human or veterinary drug applications.


?? Ordering & Support

  • Quality Assurance: Batch-specific HPLC/NMR reports available.

  • Customization: Bulk quantities (>1 g) and formulation support upon request.

  • Shipping: Dry ice packaging for international delivery.

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