14510-06-6
Chemical Structure
8-Hydroxyquinoline-2-carbaldehyde
- CAS No.: 14510-06-6
- Formula:C10H7NO2
- Molecular Weight:173.17
IUPAC Name: 8-hydroxyquinoline-2-carbaldehyde
InChIKey: SLBPIHCMXPQAIQ-UHFFFAOYSA-N
SMILES: O=CC1=NC2=C(C=C1)C=CC=C2O
Biological Activity: 8-Hydroxyquinoline-2-carbaldehyde is a quinoline derivative with the functions of DNA intercalation, hydroxyl radical scavenging and superoxide radical scavenging. 8-Hydroxyquinoline-2-carbaldehyde serves as a precursor for synthesizing Schiff base ligands with DNA intercalation activity and antioxidant properties. 8-Hydroxyquinoline-2-carbaldehyde can be used in relevant research across multiple fields including materials science and biomedicine[1][2].
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8-Hydroxyquinoline-2-carbaldehyde | 98.0% | 8-Hydroxyquinoline-2-carbaldehyde is a quinoline derivative with the functions of DNA intercalation, hydroxyl radical scavenging and superoxide radical scavenging. 8-Hydroxyquinoline-2-carbaldehyde serves as a precursor for synthesizing Schiff base ligands with DNA intercalation activity and antioxidant properties. 8-Hydroxyquinoline-2-carbaldehyde can be used in relevant research across multiple fields including materials science and biomedicine. | ||||||||||||||||||||
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References
- [1]. Liu YC, et al. Crystal structures, antioxidation and DNA binding properties of Yb(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carbaldehyde and four aroylhydrazines. Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine. 2009 Oct;22(5):733-51. [Content Brief]
- [2]. Saadeh HA, et al. Recent Advances in the Synthesis and Biological Activity of 8-Hydroxyquinolines. Molecules (Basel, Switzerland). 2020 Sep 21;25(18):4321. [Content Brief]
