141102-07-0

Basic information

• Product Name: 1-propyl-1H-indole-3-carboxylic acid
• Synonyms: 1-propyl-1H-indole-3-carboxylic acid;1H-INDOLE-3-CARBOXYLIC ACID,1-PROPYL-
• CAS NO: 141102-07-0
• Molecular Formula: C₁₂H₁₃NO₂
• Molecular Weight: 203.24
• Mol File: 141102-07-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-propyl-1H-indole-3-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-propyl-1H-indole-3-carboxylic acid(141102-07-0)
• EPA Substance Registry System: 1-propyl-1H-indole-3-carboxylic acid(141102-07-0)

Safety Data

• Hazardous Substances Data: 141102-07-0(Hazardous Substances Data)

Usage

Indole derivative

A compound based on the indole structure This compound is derived from the indole structure, which is a bicyclic aromatic organic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Propyl group attachment

At the 1-position of the indole ring A propyl group (a three-carbon alkyl chain) is attached to the first position of the indole ring in this compound.

Carboxylic acid group

At the 3-position A carboxylic acid group (a carbonyl group bonded to an oxygen atom and a hydroxyl group) is present at the third position of the compound.

Potential pharmaceutical properties

Anti-inflammatory and analgesic agent This compound has been studied for its potential to act as an anti-inflammatory and pain-relieving substance.

Applications in medicinal chemistry

Development of novel drugs The compound may have potential applications in the field of medicinal chemistry for creating new and improved drugs.

Further research needed

Pharmacological and biological properties More research is required to fully understand the properties and potential effects of 1-propyl-1H-indole-3-carboxylic acid in biological systems.

Upstream product

• 771-50-6 1H-indole-3-carboxylic acid 
• 942-24-5 3-methoxycarbonylindole 
• 858515-83-0 1-propylindole-3-carboxylic acid methyl ester 

Downstream Products

• 858515-53-4 C₃₄H₄₅N₃O₅ 

Relevant articles and documents

Synthesis and biological evaluation of novel indole derivatives containing sulfonamide scaffold as potential tubulin inhibitor

Microtubule-targeted drugs play a critical role in various types of cancer therapy worldwide. In our study, a series of novel indole derivatives containing a sulfonamide scaffold were designed, synthesized and biologically evaluated as potential tubulin p

NOVEL INDOLE AND PYRROLOPYRIDINE AMIDES

The present invention relates to indole and pyrrolopyridine amide derivatives of formula (I) wherein R1, R 2, R 3, U, V, W, X, Y, Z and ring A are as described in the description, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as orexin receptor antagonists.

Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase

A new series of novel mast cell tryptase inhibitors is reported, which features the use of an indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The best members of this series display good in vitro activity and excellent selectivity against other serine proteases.