structure of 2-(Isoquinolin-6-yl)ethanamine

2-(Isoquinolin-6-yl)ethanamine

CAS No.: 1000505-67-8
M. Wt: 172.22600
M. Fa: C11H12N2
InChI Key: KWBVZIOLYNFITQ-UHFFFAOYSA-N

Names and Identifiers of 2-(Isoquinolin-6-yl)ethanamine

CAS Number

1000505-67-8

MDL Number

MFCD09924629

IUPAC Name

2-(isoquinolin-6-yl)ethan-1-amine

InChI

InChI=1S/C11H12N2/c12-5-3-9-1-2-11-8-13-6-4-10(11)7-9/h1-2,4,6-8H,3,5,12H2

InChIKey

KWBVZIOLYNFITQ-UHFFFAOYSA-N

Canonical SMILES

NCCC1=CC=C2C=NC=CC2=C1

UNSPSC Code

12352100

Physical and chemical properties of 2-(Isoquinolin-6-yl)ethanamine

Exact Mass

172.10000

H Bond Acceptors

2

H Bond Donors

1

LogP

2.43630

Molecular Formula

C11H12N2

Molecular Weight

172.22600

PSA

38.91000

Safety Information of 2-(Isoquinolin-6-yl)ethanamine

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 2-(Isoquinolin-6-yl)ethanamine

2-(Isoquinolin-6-YL)ethanamine finds applications across various fields:

  • Medicinal Chemistry: It serves as a building block for synthesizing complex organic molecules and heterocyclic compounds with potential therapeutic effects.
  • Biological Research: Its derivatives are studied for their interactions with biological targets, contributing to drug discovery efforts.
  • Industrial Uses: The compound is also explored in the production of dyes and pigments due to its unique chemical structure.

Interaction Studies of 2-(Isoquinolin-6-yl)ethanamine

Research has focused on the interaction of 2-(Isoquinolin-6-YL)ethanamine with various biological targets:

  • Receptor Binding: Some derivatives have demonstrated the ability to bind specific receptors, influencing their activity and leading to therapeutic effects.
  • Mechanism of Action: The compound's mechanism often involves enzyme inhibition and receptor modulation, which are critical for its biological efficacy.

Biological Activity of 2-(Isoquinolin-6-yl)ethanamine

Isoquinoline derivatives, including 2-(Isoquinolin-6-YL)ethanamine, exhibit a range of biological activities:

  • Enzyme Inhibition: They have been shown to inhibit key enzymes such as DNA gyrase and topoisomerase, which are crucial for bacterial DNA replication and thus represent potential antibiotic targets.
  • Therapeutic Properties: Research indicates potential applications in treating conditions such as cancer and inflammation due to their ability to modulate biological pathways.