93-10-7
93-10-7
Chemical Structure
Quinoline-2-carboxylic acid
- CAS No.: 93-10-7
- Formula:C10H7NO2
- Molecular Weight:173.17
IUPAC Name: quinoline-2-carboxylic acid
InChIKey: LOAUVZALPPNFOQ-UHFFFAOYSA-N
SMILES: O=C(O)C1=NC(C=CC=C2)=C2C=C1
Biological Activity: Quinoline-2-carboxylic acid exhibits antidiabetic activity. Quinoline-2-carboxylic acid can be used as drug intermediate for synthesis of various active compounds[1][2].
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Quinoline-2-carboxylic acid | 99.99% | 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-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-2-carboxylic acid-d6 | Quinoline-2-carboxylic acid-d6 is the deuterium labeled Quinoline-2-carboxylic acid (HY-W002011). 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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References
- [1]. Lee H W, et al., Quinoline-2-carboxylic acid isolated from Ephedra pachyclada and its structural derivatives show inhibitory effects against α-glucosidase and α-amylase[J]. Journal of the Korean Society for Applied Biological Chemistry, 2014, 57: 441-444.
- [2]. Yang R, et al., Synthesis of Quinoline-2-Carboxylic Acid Aryl Ester and Its Apoptotic Action on PC3 Prostate Cancer Cell Line. Appl Biochem Biotechnol. 2023 Aug;195(8):4818-4831. [Content Brief]
