Names | |
---|---|
Preferred IUPAC name
4-[3-(1H-Imidazol-5-yl)propyl]piperidine | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
UNII | |
| |
| |
Properties | |
C11H19N3 | |
Molar mass | 193.288 g/mol |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
VUF-5681 is a potent and selective histamine antagonist which binds selectively to the H3 subtype. [1] However while VUF-5681 blocks the activity of more potent H3 agonists, recent studies suggest that it may have some weak partial agonist activity when administered by itself. [2]
Names | |
---|---|
Preferred IUPAC name
4-[3-(1H-Imidazol-5-yl)propyl]piperidine | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
UNII | |
| |
| |
Properties | |
C11H19N3 | |
Molar mass | 193.288 g/mol |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
VUF-5681 is a potent and selective histamine antagonist which binds selectively to the H3 subtype. [1] However while VUF-5681 blocks the activity of more potent H3 agonists, recent studies suggest that it may have some weak partial agonist activity when administered by itself. [2]