Asenapine citrate structure
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Common Name | Asenapine citrate | ||
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CAS Number | 1411867-74-7 | Molecular Weight | 477.89 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C23H24ClNO8 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Asenapine citrateAsenapine citrate, an atypical antipsychotic, is an antagonist of serotonin receptors (pKi: 8.4-10.5), adrenoceptors (pKi: 8.9-9.5), dopamine receptors (pKi: 8.9-9.4) and histamine receptors (pKi: 8.2-9.0). Asenapine citrate can be used in the research of schizophrenia and bipolar disorder[1][2]. |
Name | Asenapine citrate |
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Description | Asenapine citrate, an atypical antipsychotic, is an antagonist of serotonin receptors (pKi: 8.4-10.5), adrenoceptors (pKi: 8.9-9.5), dopamine receptors (pKi: 8.9-9.4) and histamine receptors (pKi: 8.2-9.0). Asenapine citrate can be used in the research of schizophrenia and bipolar disorder[1][2]. |
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Related Catalog | |
Target |
5-HT1A Receptor:8.6 (pKi) 5-HT1B Receptor:8.4 (pKi) 5-HT2A Receptor:10.2 (pKi) 5-HT2B Receptor:9.8 (pKi) 5-HT2C Receptor:10.5 (pKi) 5-HT5 Receptor:8.8 (pKi) 5-HT6 Receptor:9.6 (pKi) 5-HT7 Receptor:9.9 (pKi) α1-adrenergic receptor:8.9 (pKi) Alpha-2A adrenergic receptor:8.9 (pKi) Alpha-2B adrenergic receptor:9.5 (pKi) Alpha-2C adrenergic receptor:8.9 (pKi) D1 Receptor:8.9 (pKi) D2 Receptor:8.9 (pKi) D3 Receptor:9.4 (pKi) D4 Receptor:9.0 (pKi) H1 Receptor:9.0 (pKi) H2 Receptor:8.2 (pKi) |
In Vivo | Asenapine (0.05-0.2 mg/kg; s.c.) induces a dose-dependent suppression of conditioned avoidance response (CAR) and does not induce catalepsy[2]. |
References |
Molecular Formula | C23H24ClNO8 |
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Molecular Weight | 477.89 |