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Quinoline-2-carboxylic acid (Standard)

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].

Product Specifications

CAS Number

[93-10-7]

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Amylases; Glycosidase

Related Pathways

Metabolic Enzyme/Protease

Field of Research

Metabolic Disease

Purity

99.96

Smiles

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

Molecular Formula

C10H7NO2

Molecular Weight

173.17

Precautions

H302, H315, H319, H335

References & Citations

[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.

Shipping Conditions

Blue Ice

Storage Conditions

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

Scientific Category

Reference Standards

Available Sizes

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