Chinoline-2-carbonzuur (standaard)

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].

93-10-7

12352005

H302, H315, H319, H335

Amylases; Glycosidase

Metabolic Enzyme/Protease

Metabolic Disease

99.96

O=C(O)C1=NC(C=CC=C2)=C2C=C1

C10H7NO2

173.17

H302, H315, H319, H335

[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.|[3]Wade JJ, et al., Antiallergic activity of tetracyclic derivatives of quinoline-2-carboxylic acid. 2. Some benzothienoquinolinecarboxylic acids. J Med Chem. 1978 Sep;21 (9) :941-8.

Blue Ice

-20°C, sealed storage, away from light and moisture

http://file.medchemexpress.com/batch_PDF/HY-W002011R/Quinoline-2-carboxylic-acid-Standard-SDS-MedChemExpress.pdf

Reference Standards