486-74-8
486-74-8
Chemical Structure
4-Quinolinecarboxylic acid
Synonym(s): Cinchoninic acid; 4-Carboxyquinoline; NSC 13138
- CAS No.: 486-74-8
- Formula:C10H7NO2
- Molecular Weight:173.17
IUPAC Name: quinoline-4-carboxylic acid
InChIKey: VQMSRUREDGBWKT-UHFFFAOYSA-N
SMILES: O=C(C1=CC=NC2=CC=CC=C12)O
Biological Activity: 4-Quinolinecarboxylic acid (Cinchoninic acid; 4-Carboxyquinoline; NSC 13138) is a quinoline derivative and also an Endogenous Metabolite. 4-Quinolinecarboxylic acid can serve as the sole carbon source for the growth of the soil bacterium Microbacterium sp. H2[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Quinolinecarboxylic acid | 99.58% | 4-Quinolinecarboxylic acid (Cinchoninic acid; 4-Carboxyquinoline; NSC 13138) is a quinoline derivative and also an Endogenous Metabolite. 4-Quinolinecarboxylic acid can serve as the sole carbon source for the growth of the soil bacterium Microbacterium sp. H2. | ||||||||||||||||||||
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4-Quinolinecarboxylic acid (Standard) | 99.67% | 4-Quinolinecarboxylic acid (Standard) (Cinchoninic acid (Standard); 4-Carboxyquinoline (Standard); NSC 13138 (Standard)) is the analytical standard of 4-Quinolinecarboxylic acid (HY-Y0057). This product is intended for research and analytical applications. 4-Quinolinecarboxylic acid (Cinchoninic acid; 4-Carboxyquinoline; NSC 13138) is a quinoline derivative and also an Endogenous Metabolite. 4-Quinolinecarboxylic acid can serve as the sole carbon source for the growth of the soil bacterium Microbacterium sp. H2. | ||||||||||||||||||||
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References
- [1]. Röger P. Degradation of quinoline-4-carboxylic acid by Microbacterium sp. FEMS Microbiol Lett. 1989;57(3):279‐282
- [2]. Sabt A, et al. Identification of 2-(-aryl-1,2,3-triazol-4-yl) quinoline derivatives as antitubercular agents endowed with InhA inhibitory activity. Frontiers in chemistry. 2024;12:1424017. [Content Brief]
