structure of 2-(1H-indol-3-yl)propan-1-ol

2-(1H-indol-3-yl)propan-1-ol

CAS No.: 10006-92-5
M. Wt: 175.22700
M. Fa: C11H13NO
InChI Key: BQJNIKZTDTZGFT-UHFFFAOYSA-N

Names and Identifiers of 2-(1H-indol-3-yl)propan-1-ol

CAS Number

10006-92-5

IUPAC Name

2-(1H-indol-3-yl)propan-1-ol

InChI

InChI=1S/C11H13NO/c1-8(7-13)10-6-12-11-5-3-2-4-9(10)11/h2-6,8,12-13H,7H2,1H3

InChIKey

BQJNIKZTDTZGFT-UHFFFAOYSA-N

Canonical SMILES

CC(CO)C1=CNC2=CC=CC=C21

Physical and chemical properties of 2-(1H-indol-3-yl)propan-1-ol

Exact Mass

175.10000

LogP

2.26370

Molecular Formula

C11H13NO

Molecular Weight

175.22700

PSA

36.02000

Safety Information of 2-(1H-indol-3-yl)propan-1-ol

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 2-(1H-indol-3-yl)propan-1-ol

2-(1H-indol-3-yl)propan-1-ol has potential applications in various fields:

  • Pharmaceuticals: Due to its interaction with neurotransmitter receptors, it may serve as a lead compound for developing antidepressants or anxiolytics.
  • Agriculture: Its structural similarity to plant hormones suggests potential use as a growth regulator or herbicide.
  • Chemical Research: It acts as a building block for synthesizing more complex organic molecules and studying structure–activity relationships in drug design.

Interaction Studies of 2-(1H-indol-3-yl)propan-1-ol

Studies on 2-(1H-indol-3-yl)propan-1-ol have focused on its interactions with various biological targets. It has shown potential effects on neurotransmitter levels by modulating serotonin pathways, which could influence cognitive functions and mood disorders. Additionally, research indicates that it may interact with enzymes involved in metabolic pathways, thereby affecting physiological processes related to amino acid metabolism.

Biological Activity of 2-(1H-indol-3-yl)propan-1-ol

The biological activity of 2-(1H-indol-3-yl)propan-1-ol is primarily attributed to its interaction with various molecular targets. It has been shown to bind to serotonin receptors, suggesting a role in neurotransmission and mood regulation. Additionally, indole derivatives are known for their anti-inflammatory, anticancer, and antimicrobial properties. The specific mechanisms through which 2-(1H-indol-3-yl)propan-1-ol exerts its effects are still being explored, but it is hypothesized that it may influence enzyme activity and gene expression in biological systems.

Retrosynthesis analysis of 2-(1H-indol-3-yl)propan-1-ol

  • Route#1

    Cas:100-63-0
    Cas:513-42-8
    Cas:10006-92-5