3-Benzoyl-2-pyridinecarboxylic acid, also known by its CAS number 64362-32-9, is an organic compound characterized by its pyridine and carboxylic acid functional groups. This compound typically appears as a crystalline solid and is soluble in organic solvents, reflecting its aromatic nature. The presence of the benzoyl group contributes to its reactivity, making it useful in various chemical syntheses and applications, including pharmaceuticals and agrochemicals. The carboxylic acid group imparts acidic properties, allowing it to participate in acid-base reactions. Additionally, the compound may exhibit biological activity, which can be explored for potential therapeutic uses. Its structural features enable it to engage in hydrogen bonding and π-π interactions, influencing its physical properties and reactivity. Overall, 3-benzoyl-2-pyridinecarboxylic acid is a versatile compound with significant implications in organic chemistry and medicinal chemistry research.

3-benzoyl-2-pyridinecarboxylic acid

64362-32-9: 3-Benzoylpyridine-2-carboxylic acid, 2-Carboxy-3-benzoylpyridine

3-Benzoylpicolinic acid

3-Benzoyl-2-pyridinecarboxylic acid (3BPCA) is a competitive inhibitor of the enzyme aldehyde reductase. It has been shown to be active against diabetics in vitro and in vivo, as well as being able to inhibit the glucose uptake of isolated rat adipocytes. 3BPCA has also been shown to have bifunctional properties, inhibiting both the synthesis of fatty acids and glucose oxidation in vitro. The selectivity of 3BPCA is influenced by its uncompetitive inhibition of aldehyde reductase and competitive inhibition of acetyl-CoA carboxylase.

CAS 64362-32-9: 3-benzoyl-2-pyridinecarboxylic acid

3-Benzoylpicolinic acid

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3-Benzoylpicolinic acid

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3-Benzoyl-2-pyridinecarboxylicacid

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