Remoxipride hydrochloride
Modify Date: 2024-01-14 15:21:32
Remoxipride hydrochloride structure
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Common Name | Remoxipride hydrochloride | ||
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| CAS Number | 73220-03-8 | Molecular Weight | 407.73 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C16H24BrClN2O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of Remoxipride hydrochloride(S)-Remoxipride ((-)-Remoxipride) hydrochloride is a selective dopamine D2-receptor antagonist with an IC50 value of 1.57 μM. (S)-Remoxipride hydrochloride can be used for the research of psychotic disorder[1]. |
| Name | Remoxipride hydrochloride,(S)-(-)-3-Bromo-N-[(1-ethyl-2-pyrrolidinylmethyl]2,6-dimethoxybenzamidehydrochloride |
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| Synonym | More Synonyms |
| Description | (S)-Remoxipride ((-)-Remoxipride) hydrochloride is a selective dopamine D2-receptor antagonist with an IC50 value of 1.57 μM. (S)-Remoxipride hydrochloride can be used for the research of psychotic disorder[1]. |
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| Related Catalog | |
| In Vitro | (S)-Remoxipride hydrochloride (1-100 μM; 20 min) shows binding efficiency with IC50s of ＞100, 1.57 and 42 μM for dopamine D1, dopamine D2 and α1-Adrenoccptor, respectively[1]. |
| In Vivo | (S)-Remoxipride hydrochloride (0.1-100 μM/kg; i.p. 60 min prior to apomorphine) blockades apomorphine-induced behaviors s in rats and vomiting in dogs[1]. (S)-Remoxipride hydrochloride (0.1-10 mg/kg; i.p. 30 min prior to apomorphine) displaces [3H]spiperone from both striatal and extra-striatal areas[1]. |
| References |
| Molecular Formula | C16H24BrClN2O3 |
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| Molecular Weight | 407.73 |
| Exact Mass | 406.06600 |
| PSA | 50.80000 |
| LogP | 3.81120 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| HS Code | 2933990090 |
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| HS Code | 2933990090 |
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| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
| Macbecin I |
| REMOXIPRIDE HYDROCHLORIDE |