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Pharmaceutical-Grade Curculigoside (≥98% Purity) | Natural Compound for Anti-Inflammatory & Bone Health Studies

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Pharmaceutical-Grade Curculigoside (≥98% Purity) | Natural Compound for Anti-Inflammatory & Bone Health Studies

Pharmaceutical-Grade Curculigoside (≥98% Purity) | Natural Compound for Anti-Inflammatory & Bone Health Studies

Curculigoside  is a high-purity phenolic glycoside isolated from Curculigo species, extensively utilized in pharmacological research for its potent bioactivities. With HPLC-confirmed purity ≥98%, this compound serves as a critical reference standard in drug discovery and mechanistic studies.

  • Product Name :

    Curculigoside
  • CAS No. :

    85643-19-2
  • Appearance :

    White to off-white crystalline powder
  • Specification :

    98%

? Curculigoside (HPLC ≥98%) | CAS: 85643-19-2

Molecular Formula: C??H??O?? | Molecular Weight: 466.44
Appearance: White to off-white crystalline powder
Source: Curculigo glabrescens (Orchidaceae family), sustainably harvested in China


? Core Value Proposition

? Pharma-Grade Purity & Bioactivity

  • Exclusively ≥98% Pure: Rigorously verified by HPLC-ELSD, NMR, and MS, with lot-specific Certificates of Analysis (COA).

  • Bioactivity Guaranteed: Confirmed multi-target modulation of JAK/STAT/NF-κB pathways, validated via cell-based assays for anti-osteoporotic, anti-arthritic, and neuroprotective efficacy.

? Clinically Validated Benefits

  • Anti-Osteoporotic Action: Significantly enhances bone mineral density by suppressing osteoclastogenesis via RANKL/OPG pathway modulation (in vivo models).

  • Anti-Arthritic Efficacy: Reduces joint inflammation and cartilage degradation by inhibiting JAK1/JAK3/STAT3 phosphorylation (IC??: 4–16 μg/ml in MH7A cells).

  • Neuroprotection: Attenuates oxidative stress and neuronal apoptosis in neurodegenerative models (e.g., Aβ-induced toxicity).


?? Technical Specifications

Parameter Detail
Purity ≥98% (HPLC-ELSD)
Identification NMR, Mass Spectrometry
Storage 2–8°C, sealed, inert atmosphere, protected from light
Shelf Life 24 months*
Solubility DMSO (10 mM), methanol, ethanol; insoluble in water, chloroform, petroleum ether
Packaging 20 mg–10 kg (vacuum-sealed vials or GMP-compliant drums)

 


? Industry Applications

? Osteoporosis & Arthritis Therapeutics

  • Bone Health Adjuvant: Reverses glucocorticoid-induced bone loss by regulating Wnt/β-catenin and OPG/RANKL pathways.

  • Rheumatoid Arthritis Management: Suppresses synovial hyperplasia and cytokine storms (e.g., TNF-α, IL-6) via JAK/STAT inhibition.

? Neuroprotective & Anti-Inflammatory Research

  • Depression Therapy: Modulates hippocampal BDNF/TrkB signaling to exert antidepressant effects.

  • Neuroinflammation Control: Inhibits microglial activation and NF-κB-driven neurotoxicity in Parkinson’s/Alzheimer’s models.

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? Competitive Edge

Advantage Detail
Bioactivity Proof Lot-specific JAK/STAT inhibition data included
Ethical Sourcing Traceable to cultivated Curculigo glabrescens (China)
Global Compliance ISO 9001, heavy metals ≤10 ppm (USP/EP standards), Kosher-certified

? Packing & Delivery

Weight Packing Method Transport
20 mg–1 kg Amber glass vials + desiccant + dry ice DHL/FedEx (3–7 days)
1 kg–25 kg Sealed buckets with temperature loggers By Air (5–10 days)
>25 kg GMP drums (-20°C monitored) By Sea (15–45 days)

? FAQ

Q: How to validate anti-osteoporotic activity?
→ Free 20 mg samples provided with COA + in vitro osteoclastogenesis assay data.

Q: Solubility limitations for in vivo studies?
→ Cyclodextrin-complexed analogs available for enhanced aqueous solubility (OEM inquiries accepted).

Q: Stability during long-term storage?
→ Stability-tested for 24 months at 2–8°C; resealable packaging with nitrogen backfilling prevents oxidation.

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