7482-91-9

Usage

Uses

Used in Research Applications:
2-Pyridin-3-yl-quinoline-4-carboxylic acid is used as a research compound for exploring its chemical properties, potential interactions, and possible applications in various fields. Its unique molecular structure and the presence of aromatic rings and a carboxylic acid group make it an interesting subject for scientific investigation.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Pyridin-3-yl-quinoline-4-carboxylic acid is used as a starting material or intermediate in the synthesis of various drug candidates. Its aromatic and polar characteristics may contribute to the development of new therapeutic agents with specific biological activities.
Used in Chemical Synthesis:
2-Pyridin-3-yl-quinoline-4-carboxylic acid is used as a building block in the synthesis of complex organic compounds and materials. Its versatile structure allows for further functionalization and modification, enabling the creation of new molecules with tailored properties for various applications.
Used in Material Science:
In the field of material science, 2-Pyridin-3-yl-quinoline-4-carboxylic acid may be utilized in the development of novel materials with specific optical, electronic, or magnetic properties. Its aromatic and conjugated nature could contribute to the design of advanced materials for various technological applications.

InChI:InChI=1/C15H10N2O2/c18-15(19)12-8-14(10-4-3-7-16-9-10)17-13-6-2-1-5-11(12)13/h1-9H,(H,18,19)

Upstream product

• 350-03-8 methyl-3-pyridylketone 
• 91-56-5 indole-2,3-dione 
• 101714-03-8 2-oxo-4-(3-pyridyl)-3-butene-1-oic acid 
• 62-53-3 aniline 

Downstream Products

• 6294-65-1 2-pyridin-3-yl-quinoline 

Relevant academic research and scientific papers

Design of a dual sensing highly selective cyanide chemodosimeter based on pyridinium ring chemistry

A new chemodosimeter, Quino-P, recognizes the strongly nucleophilic cyanide by dual colorimetric and fluorescence 'off-on' signalling responses. Noteworthily, several other anions, even in significantly higher concentrations, induce no detectable photophysical perturbations. The chemodosimeter mechanism involves formation of a C4-cyano adduct, which exhibits an uncommon phenomenon of enhanced internal charge transfer interaction. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2011.

Quinoline-4-carboxamide skeleton derivative and application thereof

The invention discloses a quinoline-4-formamide skeleton derivative and application thereof, belonging to the field of chemical medicines. The invention provides a compound as shown in a formula I or pharmaceutically acceptable salt thereof. The invention

Discovery of Potent Small-Molecule SIRT6 Activators: Structure-Activity Relationship and Anti-Pancreatic Ductal Adenocarcinoma Activity

SIRT6 activation is thought to be a promising target for the treatment of many diseases, particularly cancer. Herein, we report the discovery of a series of new small-molecule SIRT6 activators. Structure-activity relationship analyses led to the identific

NEW ACETYL COENZYME A CARBOXYLASE (ACC) INHIBITORS AND USES IN TREATMENTS OF OBESITY AND DIABETES MELLITUS - 087

The present invention relates to Acetyl Coenzyme A Carboxylase (ACC) inhibitors according to formula (I), or an enantiomer thereof, or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, E, L, Z and n are as defined herein, to processes for preparing such compounds, to pharmaceutical compositions containing them, to the use of such inhibitors and to methods for th eir therapeutic use, particularly in the treatments of obesity and diabetes mellitus.

Cytochrome P450 2C9 type II binding studies on quinoline-4-carboxamide analogues

CYP2C9 is a significant P450 protein responsible for drug metabolism. With the increased use of heterocyclic compounds in drug design, a rapid and efficient predrug screening of these potential type II binding compounds is essential to avoid adverse drug