CAS 39111-94-9
:3-(quinolin-2-yl)propanoic acid
Description:
3-(Quinolin-2-yl)propanoic acid is an organic compound characterized by its quinoline moiety, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. This compound features a propanoic acid functional group, contributing to its acidic properties. It typically appears as a solid at room temperature and is soluble in polar solvents due to the presence of the carboxylic acid group. The compound is of interest in various fields, including medicinal chemistry, due to its potential biological activities, such as antimicrobial or anti-inflammatory effects. Its structure allows for interactions with biological targets, making it a candidate for drug development. Additionally, the presence of the quinoline ring can enhance its pharmacological properties. As with many organic acids, it may exhibit behavior such as protonation and deprotonation depending on the pH of the environment. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C12H11NO2
InChI:InChI=1/C12H11NO2/c14-12(15)8-7-10-6-5-9-3-1-2-4-11(9)13-10/h1-6H,7-8H2,(H,14,15)
SMILES:c1ccc2c(c1)ccc(CCC(=O)O)n2
Synonyms:- 2-Quinolinepropanoic Acid
- 3-Quinolin-2-Ylpropanoic Acid
- 3-(Quinolin-2-yl)propanoic acid
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Found 5 products.
3-Quinolin-2-ylpropanoic acid
CAS:Formula:C12H11NO2Purity:97%Color and Shape:SolidMolecular weight:201.22123-(quinolin-2-yl)propanoic Acid
CAS:Controlled Product<p>Applications 3-(quinolin-2-yl)propanoic acid (cas# 39111-94-9) is a useful research chemical for biological study. In particular it has been used in identifying structure-activity relationship of HDAC6 zinc-finger ubiquitin binding domain inhibitors.<br>References Ferreira, F., et al.: J. Med. Chem, 61, 4517 (2018)<br></p>Formula:C12H11NO2Color and Shape:Light Brown To BrownMolecular weight:201.223-(Quinolin-2-yl)propanoic acid
CAS:<p>3-(Quinolin-2-yl)propanoic acid is a quinoline derivative that is used to treat inflammatory diseases. It is thought to have an anti-inflammatory effect by inhibiting the production of the fatty acid arachidonic acid, which is then converted into prostaglandins and leukotrienes. 3-(Quinolin-2-yl)propanoic acid inhibits cellular signaling by binding to specific protein receptors. This drug binds to the fatty acids in cell membranes, which leads to the inhibition of cellular growth factor signal transduction and signal detection. Research has shown that 3-(quinolin-2-yl)propanoic acid has a toxic effect on humans, as well as other animals, including rats and mice. The animal studies showed that this drug inhibited the growth of cancer cells in human colon tumors.</p>Formula:C12H11NO2Purity:Min. 95%Molecular weight:201.22 g/mol





