structure of 2-(3-Methoxypropyl)guanidine

2-(3-Methoxypropyl)guanidine

CAS No.: 100056-66-4
M. Wt: 131.17600
M. Fa: C5H13N3O
InChI Key: QVZVXYGKHDSKKK-UHFFFAOYSA-N

Names and Identifiers of 2-(3-Methoxypropyl)guanidine

CAS Number

100056-66-4

IUPAC Name

2-(3-methoxypropyl)guanidine

InChI

InChI=1S/C5H13N3O/c1-9-4-2-3-8-5(6)7/h2-4H2,1H3,(H4,6,7,8)

InChIKey

QVZVXYGKHDSKKK-UHFFFAOYSA-N

Canonical SMILES

COCCCN=C(N)N

Physical and chemical properties of 2-(3-Methoxypropyl)guanidine

Exact Mass

131.10600

LogP

0.69690

Molecular Formula

C5H13N3O

Molecular Weight

131.17600

PSA

71.13000

Applications of 2-(3-Methoxypropyl)guanidine

2-(3-Methoxypropyl)guanidine has several promising applications:

  • Pharmaceuticals: Its potential as a therapeutic agent makes it a candidate for drug development, especially in treating metabolic disorders or cancers.
  • Biochemical Research: The compound can serve as a biochemical probe to study guanidine-related pathways and mechanisms in biological systems.
  • Catalysis: Due to its guanidine functional group, it may also find applications in catalysis, particularly in organic synthesis.

Interaction Studies of 2-(3-Methoxypropyl)guanidine

Studies on 2-(3-Methoxypropyl)guanidine's interactions with biological molecules are crucial for understanding its mechanism of action. Interaction studies often focus on:

  • Enzyme Inhibition: Investigating how this compound affects enzyme activity and whether it can serve as a selective inhibitor.
  • DNA Binding: Analyzing its ability to bind DNA or RNA molecules, which is critical for its potential use in cancer therapy.
  • Receptor Modulation: Examining how it interacts with specific receptors involved in metabolic pathways.

Biological Activity of 2-(3-Methoxypropyl)guanidine

Research indicates that 2-(3-Methoxypropyl)guanidine exhibits significant biological activity, particularly in the field of pharmacology. Its structural characteristics allow it to interact with various biological targets, including enzymes and receptors. For instance, guanidine derivatives are often investigated for their potential as enzyme inhibitors and modulators in metabolic pathways.

In specific studies, compounds similar to 2-(3-Methoxypropyl)guanidine have shown moderate antiproliferative effects against cancer cell lines, suggesting potential applications in oncology. The mechanism of action typically involves interference with cellular signaling pathways or direct interaction with DNA.