Description
IUPAC Name: 5,6,7-trihydroxy-2-phenylchromen-4-one
InChI: InChI=1S/C15H10O5/c16-9-6-11(8-4-2-1-3-5-8)20-12-7-10(17)14(18)15(19)13(9)12/h1-7,17-19H
InChIKey: FXNFHKRTJBSTCS-UHFFFAOYSA-N
Canonical SMILES: C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O
Isomeric SMILES: C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O
Synonyms: baicalein; 491-67-8; 5,6,7-Trihydroxyflavone; Noroxylin; 5,6,7-trihydroxy-2-phenyl-4H-chromen-4-one; Biacalein; BaiKalein; 5,6,7-trihydroxy-2-phenylchromen-4-one; …
Botanical Source: Scutellariae radix
Product Overview
BIORLAB provides high-purity Baicalein, a bioactive flavone with significant applications in anti-inflammatory, anticancer, and neuroprotective research. The latest research demonstrates its diverse therapeutic potential.
Technical Specifications
- Molecular Formula: C₁₅H₁₀O₅
- Source: Scutellaria baicalensis
- Appearance: Yellow crystalline powder
- Purity: ≥98% (HPLC)
- Storage: -20°C, protected from light
Research Applications
Primary Research Areas
- Anti-neoplastic studies
- Anti-inflammatory research
- Neuroprotection studies
- Cardiovascular research
Key Research Properties
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Cancer Research Applications
- Cell apoptosis studies
- Cell cycle arrest
- Metastasis inhibition
- Angiogenesis regulation
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Biological Activities
- Multiple signaling pathway modulation
- Immune microenvironment regulation
- Metabolism modulation
- Autophagy regulation
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
Technical Support Features
- Method development assistance
- Analytical testing guidance
- Stability data available
- Research protocol support
For detailed technical information, bulk quantities, or custom requirements, contact BIORLAB’s scientific team.
Note: This product is intended for laboratory research purposes only.