52980-10-6

Basic information

• Product Name: 2-Quinolinecarboxylicacid,6-amino-1,4-dihydro-4-oxo-(9CI)
• Synonyms: 2-Quinolinecarboxylicacid,6-amino-1,4-dihydro-4-oxo-(9CI);6-AMino-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid
• CAS NO: 52980-10-6
• Molecular Formula: C₁₀H₈N₂O₃
• Molecular Weight: 204.18212
• Product Categories: AMINOACID
• Mol File: 52980-10-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-Quinolinecarboxylicacid,6-amino-1,4-dihydro-4-oxo-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Quinolinecarboxylicacid,6-amino-1,4-dihydro-4-oxo-(9CI)(52980-10-6)
• EPA Substance Registry System: 2-Quinolinecarboxylicacid,6-amino-1,4-dihydro-4-oxo-(9CI)(52980-10-6)

Safety Data

• Hazardous Substances Data: 52980-10-6(Hazardous Substances Data)

Usage

General Description

2-Quinolinecarboxylicacid,6-amino-1,4-dihydro-4-oxo-(9CI) is a chemical compound that belongs to the quinoline carboxylic acid group. It is a derivative of quinoline, which is a heterocyclic aromatic compound. This chemical contains an amino group and a carbonyl group, making it a versatile molecule for various applications in organic chemistry. It may be used as a building block in the synthesis of pharmaceuticals or in the development of new chemical compounds with potential pharmacological or biological activities. Overall, this chemical has potential for use in the synthesis of various organic compounds and may have applications in the pharmaceutical or chemical industries.

Upstream product

• 100-01-6 4-nitro-aniline 
• 16133-46-3 methyl 1,4-dihydro-6-nitro-4-oxo-2-quinolinecarboxylate 
• 16133-44-1 dimethyl 2-<(4-nitrophenyl)amino>-2-butenedioate 
• 24782-43-2 ethyl 4-hydroxyquinoline-2-carboxylate 
• 52144-24-8 4-hydroxy-6-nitro-quinoline-2-carboxylic acid ethyl ester 
• 859982-04-0 6-acetylamino-4-hydroxy-quinoline-2-carboxylic acid ethyl ester 
• 52979-42-7 6-amino-4-hydroxy-2-methoxycarbonylquinoline 
• 52979-42-7 methyl 6-amino-1,4-dihydro-4-oxo-2-quinolinecarboxylate 

Downstream Products

• 874497-95-7 N-(4-amino-[6]quinolyl)-acetamide 
• 40107-09-3 4,5-Diamino-chinolin 
• 56717-02-3 6-amino-quinolin-4-ol 

Relevant articles and documents

ANTIBODIES AGAINST SEROTONIN, TRYPTOPHAN AND KYNURENINE METABOLITES AND USES THEREOF

The present invention provides antibodies and methods for preparing antibodies to metabolites in the serotonin, tryptophan and kynurenine pathways, such as 5- hydroxyindole-3-acetic acid (5-HIAA), melatonin (MT) and kynurenic acid (KYNA). The specific metabolite antibodies have low cross-reactivity to structurally related metabolites, and are useful reagents for specific and sensitive immunoassays. The present invention also provides methods for using such antibodies to measure the levels of 5-HIAA, melatonin, or kynurenic acid in biological samples from human patients.

2-AMINOCARBONYL-QUINOLINE COMPOUNDS AS PLATELET ADENOSINE DIPHOSPHATE RECEPTOR ANTAGONISTS

Compounds of formula (I), where m, n, R1, R2, R3, R4 and R6 are described herein, are useful as inhibitors of platelet adenosine diphosphate. Pharmaceutical compositions containing these compounds, methods of using these compounds as antithrombotic agents and processes for synthesizing these compounds are also described herein.

Kynurenic acid derivatives inhibit the binding of nerve growth factor (NGF) to the low-affinity p75 NGF receptor

The ability of a series of substituted kynurenic acids, thienopyridinonecarboxylic acids, and related compounds to inhibit the binding of nerve growth factor (NGF) to the p75 NGF receptor (NGFR) was evaluated in a radioligand binding assay that utilized a