Description
IUPAC Name: 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
InChI: InChI=1S/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-27,29-30H,6H2/t13-,15+,17+,18-,21+/m1/s1
InChIKey: OVSQVDMCBVZWGM-DTGCRPNFSA-N
Canonical SMILES: C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O
Isomeric SMILES: C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H]([C@H]([C@H](O4)CO)O)O)O)O)O
Synonyms: Hyperoside; 482-36-0; Hyperin; Hyperosid; Quercetin 3-galactoside; Hyperozide; Quercetin-3-O-galactoside; Quercetin-3-galactoside; …
Botanical Source: A. venetum L.
Product Overview
BIORLAB presents high-purity Hyperoside, a flavonol glycoside found in various plants including Crataegus pinnatifida Bge, Forsythia suspensa, and Cuscuta chinensis Lam, with significant therapeutic applications.
Research Applications
Primary Research Areas
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Therapeutic Applications
- Anticancer studies
- Anti-inflammatory research
- Antibacterial investigations
- Antiviral studies
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Disease Research
- Sepsis
- Arthritis
- Colitis
- Diabetic nephropathy
- Myocardial ischemia-reperfusion
- Pulmonary fibrosis
Biological Activities
Key Properties
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Primary Effects
- Antioxidant activity
- Anti-inflammatory effects
- Antidepressant properties
- Organ protective effects
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Clinical Applications
- Cancer treatment
- Inflammatory conditions
- Depression management
- Organ protection
Quality Assurance
- Full spectroscopic characterization
- Comprehensive Certificate of Analysis
- Batch-specific HPLC profiles
- Research-grade documentation
Storage & Handling
- Store at -20°C
- Protect from light
- Available in research quantities
- Stability data provided
For detailed technical information, bulk quantities, or custom requirements, contact BIORLAB’s scientific team.
Note: This product is intended for laboratory research purposes only.