Hexahydropyrrolo[1,2-a]pyrazin-4(1H)-one
CAS No.:
1000577-63-8
M. Wt:
140.183
M. Fa:
C7H12N2O
InChI Key:
HAAZJWVQKLGNDT-UHFFFAOYSA-N
Appearance:
Colorless Liquid
Names and Identifiers of 1000577-63-8
CAS Number |
1000577-63-8 |
|---|---|
EC Number |
837-079-3 |
IUPAC Name |
2,3,6,7,8,8a-hexahydro-1H-pyrrolo[1,2-a]pyrazin-4-one |
InChI |
InChI=1S/C7H12N2O/c10-7-5-8-4-6-2-1-3-9(6)7/h6,8H,1-5H2 |
InChIKey |
HAAZJWVQKLGNDT-UHFFFAOYSA-N |
Canonical SMILES |
C1CC2CNCC(=O)N2C1 |
Physical and chemical properties of 1000577-63-8
Boiling Point |
284.4±29.0 °C at 760 mmHg |
|---|---|
Density |
1.2±0.1 g/cm3 |
Exact Mass |
140.094955 |
Flash Point |
125.8±24.3 °C |
Index of Refraction |
1.551 |
LogP |
-1.13 |
Molecular Formula |
C7H12N2O |
Molecular Weight |
140.183 |
PSA |
32.34000 |
Vapour Pressure |
0.0±0.6 mmHg at 25°C |
Safety Information of 1000577-63-8
Applications of 1000577-63-8
Hexahydropyrrolo[1,2-a]pyrazin-4(1H)-one and its derivatives have several applications, particularly in medicinal chemistry:
- Drug Development: Due to its biological activity, it serves as a lead compound for developing new pharmaceuticals targeting various diseases.
- Chemical Probes: Its unique structure makes it suitable for use as a chemical probe in biological studies.
- Synthetic Intermediates: It acts as an intermediate in the synthesis of more complex organic molecules used in research and industry.
Interaction Studies of 1000577-63-8
Interaction studies involving hexahydropyrrolo[1,2-a]pyrazin-4(1H)-one focus on its binding affinities with various biological targets:
- Receptor Binding Studies: Investigations into how this compound interacts with specific receptors can help elucidate its mechanism of action and therapeutic potential.
- Enzyme Inhibition Studies: Research has indicated that certain derivatives may act as inhibitors for specific enzymes involved in disease pathways, providing insights into their pharmacological profiles.
Biological Activity of 1000577-63-8
Research indicates that hexahydropyrrolo[1,2-a]pyrazin-4(1H)-one exhibits various biological activities. Its derivatives have shown promise as:
- Antimicrobial Agents: Some studies suggest that compounds derived from hexahydropyrrolo[1,2-a]pyrazin-4(1H)-one possess antimicrobial properties, making them candidates for further development as antibiotics.
- Anticancer Activity: Certain derivatives have demonstrated cytotoxic effects against cancer cell lines, indicating potential as anticancer agents.
- Neuroprotective Effects: There is emerging evidence of neuroprotective properties, which could be beneficial in treating neurodegenerative diseases.
