(–)-IHCH7041
Modify Date: 2024-01-11 17:00:28
(–)-IHCH7041 structure
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Common Name | (–)-IHCH7041 | ||
|---|---|---|---|---|
| CAS Number | 1599089-55-0 | Molecular Weight | 184.283 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C10H20N2O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of (–)-IHCH7041(–)-IHCH7041 is a potent, selective partial agonist at DRD2/3 and 5-HT1AR, EC50 of 1.38 nM in Gαi1–γ9 dissociation and 2.75 nM in β-arrestin2 recruitment assays, with negligible 5-HT2AR binding (>100-fold selectivity).(–)-IHCH7041 exhibits negligible affinities for a large number of tested GPCRs, ion channels and transporters (Ki>500 nM), good affinities for DRD2 and DRD3 (Ki=14.42 nM), and moderate binding to 5-HT1A (Ki=60.62 nM).(–)-IHCH7041 behaves as a partial agonist in both G-protein signaling and β-arrestin recruitment activities at DRD2, DRD3 and 5-HT1AR.(–)-IHCH7041 displayed potent antipsychotic activity and has antidepressant properties and reverses cognitive impairmentin mice. |
| Name | (–)-IHCH7041 |
|---|
| Description | (–)-IHCH7041 is a potent, selective partial agonist at DRD2/3 and 5-HT1AR, EC50 of 1.38 nM in Gαi1–γ9 dissociation and 2.75 nM in β-arrestin2 recruitment assays, with negligible 5-HT2AR binding (>100-fold selectivity).(–)-IHCH7041 exhibits negligible affinities for a large number of tested GPCRs, ion channels and transporters (Ki>500 nM), good affinities for DRD2 and DRD3 (Ki=14.42 nM), and moderate binding to 5-HT1A (Ki=60.62 nM).(–)-IHCH7041 behaves as a partial agonist in both G-protein signaling and β-arrestin recruitment activities at DRD2, DRD3 and 5-HT1AR.(–)-IHCH7041 displayed potent antipsychotic activity and has antidepressant properties and reverses cognitive impairmentin mice. |
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| References | 1. Zhangcheng Chen, et al. Nat Neurosci. 2022 Jan;25(1):39-49. |
| Molecular Formula | C10H20N2O |
|---|---|
| Molecular Weight | 184.283 |