CAS 7509-13-9
:1,2-Dihydro-1-oxo-3-isoquinolinecarboxylic acid
Description:
1,2-Dihydro-1-oxo-3-isoquinolinecarboxylic acid, with the CAS number 7509-13-9, is a chemical compound characterized by its isoquinoline structure, which is a bicyclic compound containing a benzene ring fused to a pyridine ring. This substance typically exhibits properties associated with both aromatic and heterocyclic compounds, including potential biological activity. It is often studied for its role in medicinal chemistry, particularly due to its ability to interact with various biological targets. The presence of the carboxylic acid functional group suggests it can participate in acid-base reactions and may form salts or esters. Additionally, the compound's keto group contributes to its reactivity and stability under certain conditions. Its solubility and behavior in different solvents can vary, influencing its applications in synthesis and drug development. Overall, 1,2-Dihydro-1-oxo-3-isoquinolinecarboxylic acid is of interest for its structural features and potential pharmacological properties.
Formula:C10H7NO3
InChI:InChI=1S/C10H7NO3/c12-9-7-4-2-1-3-6(7)5-8(11-9)10(13)14/h1-5H,(H,11,12)(H,13,14)
InChI key:InChIKey=KYWCUACNBIYDNL-UHFFFAOYSA-N
SMILES:O=C1C=2C(C=C(C(O)=O)N1)=CC=CC2
Synonyms:- 1,2-Dihydro-1-oxo-3-isoquinolinecarboxylic acid
- 1-Hydroxyisoquinoline-3-carboxylic acid
- 3-Isoquinolinecarboxylic Acid, 1,2-Dihydro-1-Oxo-
- Isocarbostyril-3-carboxylic acid
- NSC 131339
- NSC 407253
- 1-Oxo-1,2-dihydroisoquinoline-3-carboxylic acid
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Found 4 products.
1-Oxo-1,2-dihydroisoquinoline-3-carboxylic acid
CAS:Formula:C10H7NO3Purity:95%Color and Shape:SolidMolecular weight:189.16751-Oxo-1,2-dihydroisoquinoline-3-carboxylic acid
CAS:<p>1-Oxo-1,2-dihydroisoquinoline-3-carboxylic acid</p>Purity:≥95%Molecular weight:189.17g/mol1-Oxo-1,2-dihydroisoquinoline-3-carboxylic acid
CAS:<p>1-Oxo-1,2-dihydroisoquinoline-3-carboxylic acid (ODHC) is a synthetic compound that has been shown to have anti-tumor activity in mouse melanoma cells. ODHC inhibits the production of aldehydes through the interaction with thiourea and homophthalic acid. ODHC also binds to topoisomerase II, which prevents the unwinding of DNA and limits DNA replication. This leads to cell death by inhibition of DNA synthesis. ODHC has been shown to be photostable and has a low toxicity for healthy cells. It is also able to chelate metal ions, such as iron, copper, or zinc, which are important for cancer cell growth and proliferation.</p>Formula:C10H7NO3Purity:Min. 95%Molecular weight:189.17 g/mol



