Description
IUPAC Name: 7-hydroxy-6-methoxychromen-2-one
InChI: InChI=1S/C10H8O4/c1-13-9-4-6-2-3-10(12)14-8(6)5-7(9)11/h2-5,11H,1H3
InChIKey: RODXRVNMMDRFIK-UHFFFAOYSA-N
Canonical SMILES: COC1=C(C=C2C(=C1)C=CC(=O)O2)O
Isomeric SMILES: COC1=C(C=C2C(=C1)C=CC(=O)O2)O
Synonyms: scopoletin; 92-61-5; Gelseminic acid; 7-Hydroxy-6-methoxy-2H-chromen-2-one; 6-Methylesculetin; Chrysatropic acid; Murrayetin; Scopoletine; …
Botanical Source: Hedyotis Diffusae Herba
Product Overview
BIORLAB presents high-purity Scopoletin, a naturally occurring coumarin with significant applications in pharmacological research, particularly for its therapeutic and chemopreventive properties.
Technical Specifications
- Chemical Formula: C₁₀H₈O₄
- Source: Various medicinal and edible plants
- Classification: Coumarin compound
- Storage: -20°C, protected from light
Key Research Applications
Primary Research Areas
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Therapeutic Research
- Antioxidant studies
- Antimicrobial investigations
- Anticancer research
- Anti-inflammatory studies
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Disease Research
- Cancer prevention
- Inflammatory conditions
- Metabolic disorders
- Neurological studies
Research Significance
Biological Activities
-
Pharmacological Effects
- Multiple cellular targets
- Signal pathway modulation
- Disease prevention
- Therapeutic potential
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Health Benefits
- Disease treatment
- Preventive properties
- Multiple therapeutic targets
- Broad spectrum activity
Technical Applications
Biosynthesis & Extraction
- Multiple plant sources
- Various extraction methods
- Biosynthetic pathways
- Quality control protocols
Storage & Handling
- Store at -20°C
- Protect from light
- Available in research quantities
- Stability data provided
Quality Assurance
- Full spectroscopic characterization
- Comprehensive Certificate of Analysis
- Batch-specific HPLC profiles
- Research-grade documentation
For detailed technical information, bulk quantities, or custom requirements, contact BIORLAB’s scientific team.
Note: This product is intended for laboratory research purposes only.