Salidroside
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Specification
Test Items |
Standard |
Salidroside (CAS: 10338-51-9) |
98% by HPLC |
Loss on drying |
≤3.0% |
Residue on ignition |
≤1.0% |

Natural Source

Multi-Target Action

Rapid Absorption
1.Molecular Target Network

2. Pharmacokinetics
Absorption
68% oral bioavailability (glucose transporter-mediated).
Distribution
Brain/plasma ratio = 1.5:1 (BBB-penetrant).
Metabolism
Gut microbiota hydrolyzes to tyrosol (active metabolite).
Excretion
80% urinary excretion (t½ = 2.5 h).
Clinical Applications
Indications & Protocols
Condition |
Regimen |
Evidence |
Chronic Fatigue Syndrome |
200 mg/day ×4 weeks |
↓40% fatigue score* |
Mild Cognitive Impairment |
100 mg bid ×6 months |
↑3 MMSE points |
Altitude Sickness Prevention |
300 mg/day (3 days pre-ascent) |
↑8% SpO₂ |
*Randomized double-blind trial (n=150)
Special Populations
Hepatic Impairment: Reduce dose 30% (Child-Pugh B).
Pediatrics: 12–18 years (5 mg/kg/day).
Dosage and Administration
Formulations
Tablets: 50 mg/tablet (microcrystalline cellulose).
Oral Solution: 10 mg/mL (flavored).
Injection: 20 mg/2 mL (research use).
Dosing Guidelines
Use |
Dose |
Duration |
Anti-Fatigue |
100–200 mg/day |
2–4 weeks |
Neuroprotection |
50–100 mg bid |
3–6 months |
Acute Hypoxia |
300 mg loading dose |
Short-term |
Safety Evaluation
Adverse Reactions
System |
Incidence |
Manifestations |
Gastrointestinal |
3% |
Mild nausea |
Neurological |
1% |
Transient dizziness |
Hypersensitivity |
0.1% |
Rash |
Contraindications & Interactions
Absolute CI:
Phenylethanoid allergy.
Severe hypotension (SBP <85 mmHg).
Cautions:Antidepressants (synergistic 5-HT activation).
Research Progress Green max
Novel Formulations
Nano-Crystalline Self-Stabilizing System: ↑Bioavailability to 85%.
Sublingual Fast-Dissolving Tablets: 5-min onset (for acute altitude sickness).
New Indications
Post-COVID Fatigue: Phase II trials ongoing.
Parkinson’s Disease: Protects dopaminergic neurons (↑30% TH+ cells in animals).
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