structure of 3-[(6-Chloro-[1,3]dioxolo[4,5-g]quinolin-7-ylmethyl)-amino]-propan-1-ol

3-[(6-Chloro-[1,3]dioxolo[4,5-g]quinolin-7-ylmethyl)-amino]-propan-1-ol

CAS No.: 1000348-12-8
M. Wt: 294.73
M. Fa: C14H15ClN2O3
InChI Key: -

Names and Identifiers of 1000348-12-8

CAS Number

1000348-12-8

IUPAC Name

3-[(6-chloranyl-[1,3]dioxolo[4,5-g]quinolin-7-yl)methylamino]propan-1-ol

Canonical SMILES

C1OC2=CC3=CC(=C(N=C3C=C2O1)Cl)CNCCCO

Physical and chemical properties of 1000348-12-8

Molecular Formula

C14H15ClN2O3

Molecular Weight

294.73

Applications of 1000348-12-8

This compound has potential applications in various fields:

  • Pharmaceutical Development: Due to its biological activities, it may serve as a lead compound for developing new antiviral or antimicrobial drugs.
  • Chemical Probes: It can be utilized in biological research as a chemical probe to study specific pathways or mechanisms due to its ability to interact with biological targets.

Interaction Studies of 1000348-12-8

Interaction studies are crucial for understanding how 3-[(6-Chloro-[1,3]dioxolo[4,5-g]quinolin-7-ylmethyl)-amino]-propan-1-ol interacts with biological systems. Key areas of focus include:

  • Protein Binding: Investigating how this compound binds to specific proteins can elucidate its mechanism of action.
  • Metabolic Pathways: Understanding its metabolism can help predict its pharmacokinetic properties and potential side effects.

Biological Activity of 1000348-12-8

Research indicates that compounds containing quinoline structures often exhibit significant biological activities, including:

  • Antiviral Properties: Quinoline derivatives have been studied for their potential as antiviral agents, particularly against RNA viruses .
  • Antimicrobial Activity: Many quinoline-based compounds show efficacy against various bacterial strains, making them candidates for antibiotic development.
  • Anticancer Effects: Some studies suggest that quinoline derivatives can induce apoptosis in cancer cells, highlighting their potential in cancer therapy.