Description
IUPAC Name: 3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one
InChI: InChI=1S/C16H12O7/c1-22-11-4-7(2-3-9(11)18)16-15(21)14(20)13-10(19)5-8(17)6-12(13)23-16/h2-6,17-19,21H,1H3
InChIKey: IZQSVPBOUDKVDZ-UHFFFAOYSA-N
Canonical SMILES: COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O
Isomeric SMILES: COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O
Synonyms: Isorhamnetin; 480-19-3; 3-Methylquercetin; Isorhamnetol; Quercetin 3′-methyl ether; 3′-Methoxyquercetin; 3′-O-Methylquercetin; isorhamnetine; …
Botanical Source: Hippophae rhamnoides L.
Product Overview
Isorhamnetin is a powerful O-methylated flavonol, structurally related to quercetin, with significant antioxidant and anti-inflammatory properties. BIORLAB provides high-purity isorhamnetin isolated through advanced chromatographic techniques for pharmaceutical and biomedical research.
Technical Specifications
- Molecular Formula: C₁₆H₁₂O₇
- Molecular Weight: 316.26 g/mol
- Appearance: Yellow crystalline powder
- Solubility: Soluble in DMSO, methanol, ethanol
- Melting Point: 307-309°C
Storage and Handling
- Store at -20°C in sealed containers
- Protect from light and moisture
- Stability: 2 years when properly stored
- Stock solution: Prepare in DMSO
- Avoid repeated freeze-thaw cycles
Key Research Applications
Antioxidant Research
- Free radical scavenging studies
- Oxidative stress protection
- Lipid peroxidation inhibition
- Cellular defense mechanisms
Anti-inflammatory Studies
- Cytokine modulation
- NF-κB pathway investigation
- COX-2 inhibition research
- Inflammatory mediator regulation
Cancer Research
- Anti-proliferative studies
- Apoptosis mechanisms
- Cell cycle regulation
- Signal transduction pathways
Quality Assurance
- HPLC purity analysis
- Structure verified by NMR
- Complete Certificate of Analysis
- Batch-specific documentation
- Stringent quality control
Research Benefits
- High biological activity
- Excellent batch consistency
- Comprehensive documentation
- Enhanced stability
- Superior purity
Research Applications Highlights
-
Cellular Protection
- ROS scavenging
- Antioxidant enzyme modulation
- Membrane stability
- DNA protection
-
Molecular Mechanisms
- Signal transduction
- Gene expression
- Protein interactions
- Enzyme modulation
-
Therapeutic Potential
- Cancer research
- Cardiovascular studies
- Neurological research
- Anti-aging investigations
Why Choose BIORLAB’s Isorhamnetin?
- Industry-leading purity
- Expert technical support
- Full analytical documentation
- Competitive Pricing
- Global shipping capability
- Custom synthesis options
Technical Support
- Method development assistance
- Analytical protocols
- Stability data
- Storage recommendations
- Application Guidance
For research use only. Not for human consumption or therapeutic use.