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.