7250-53-5
7250-53-5
Chemical Structure
5-Quinolinecarboxylic acid
- CAS No.: 7250-53-5
- Formula:C10H7NO2
- Molecular Weight:173.17
IUPAC Name: Quinoline-5-carboxylic acid
InChIKey: RAYMXZBXQCGRGX-UHFFFAOYSA-N
SMILES: O=C(O)C1=CC=CC2=C1C=CC=N2
Biological Activity: 5-Quinolinecarboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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5-Quinolinecarboxylic acid | 5-Quinolinecarboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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IOX1 | 99.89% | IOX1, a chemical probe, is a potent broad‐spectrum inhibitor of 2OG oxygenases, including the JmjC demethylases. IOX1 inhibits KDM4C, KDM4E, KDM2A, KDM3A and KDM6B with IC50 values of 0.6 μM, 2.3 μM, 1.8 μM, 0.1 μM and 1.4 μM, respectively. IOX1 also inhibits ALKBH5. | ||||||||||||||||||||
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3-Isoquinolinecarboxylic acid | 3-Isoquinolinecarboxylic acid (compound 2) is a synthetic intermediate that has been used to design antitumor compounds. | |||||||||||||||||||||
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Quininic acid | 99.94% | Quininic acid, purified from Eucalyptus globulus, cinchona bark, and other plant products, is the most abundant organic acid. | ||||||||||||||||||||
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Quinoline-2-carboxylic acid (Standard) | 99.96% | Quinoline-2-carboxylic acid exhibits antidiabetic activity. Quinoline-2-carboxylic acid can be used as drug intermediate for synthesis of various active compounds. | ||||||||||||||||||||
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Quinoline-6-carboxylic acid | Quinoline-6-carboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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Quinoline-8-carboxylic acid | 99.46% | Quinoline-8-carboxylic acid is a herbicide. | ||||||||||||||||||||
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1-Hydroxy-2-naphthoic acid | 99.78% | 1-Hydroxy-2-naphthoic acid is a ubiquitous bicyclic intermediate metabolite in the microbial degradation process of polycyclic aromatic hydrocarbons (PAHs). 1-Hydroxy-2-naphthoic acid can be converted into 1,2-naphthalenediol, which enters the naphthalene degradation pathway and participates in the tricarboxylic acid (TCA) cycle to achieve complete mineralization. | ||||||||||||||||||||
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7-Bromoquinoline-4-carboxylic acid | 7-Bromoquinoline-4-carboxylic acid is an organic compound primarily used for chemical synthesis. | |||||||||||||||||||||
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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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1-Naphthoic acid | 99.93% | Naphthalene-1-carboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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