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Salidroside
Natural API

Salidroside

Salidroside, the primary active compound of Rhodiola rosea (Crassulaceae family), is a phenylethanoid glycoside with CAS number 10338-51-9. Known for its ​anti-fatigue, anti-hypoxia, neuroprotective, and antidepressant​ effects, it was listed in the European Medicines Agency (EMA) traditional herbal medicine registry in 2022 and serves as a quality control marker for Rhodiola in the Chinese Pharmacopoeia (2020 edition).

Product Name: Salidroside

IUPAC Name: 2-(4-Hydroxyphenyl)ethyl-β-D-glucopyranoside

CAS No.​: 10338-51-9

Molecular Formula: C₁₄H₂₀O₇

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    Salidroside

    Basic information

    Product Name: Salidroside

    IUPAC Name: 2-(4-Hydroxyphenyl)ethyl-β-D-glucopyranoside

    CAS No.​: 10338-51-9

    Molecular Formula: C₁₄H₂₀O₇

    Physicochemical Properties:

    Parameter

    Value/Description

    ​Appearance​

     White powder

    ​Melting Point​

    159–161°C

    ​Solubility​

    50 mg/mL in water; soluble in methanol/ethanol

    ​logP​

    -0.7 (high hydrophilicity)

    ​Optical Rotation​

    [α]²⁵D = -42° (c=1, water)

    ​Stability​

    Stable at pH 3–7; light-sensitive

    Quality Standard: CP2020,JP,Customer Made

    Specification

    Test Items

    Standard

    Salidroside (CAS: 10338-51-9)

    98% by HPLC

    Loss on drying

    ≤3.0%

    Residue on ignition

    ≤1.0%

    Key Features

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    Natural Source

    0.5–3% in Rhodiola roots (higher in high-altitude varieties).
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    Multi-Target Action

    Modulates HIF-1α, BDNF, and SIRT1 pathways.
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    Rapid Absorption

    Peak plasma concentration in 30 min (Tmax = 0.5 h).

    Pharmacological Mechanisms

    1.Molecular Target Network

    Pharmacological Mechanisms6

    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).

    Rhodiola Rosea

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