| Bioactivity | Eticlopride hydrochloride, a selective dopamine D2‐like receptor antagonist, exhibits high affinity for dopamine D2, α1‐adrenergic, α2‐adrenergic, 5HT1, 5HT2 receptors with Kis of 0.09, 112, 699, 6220, and 830 nM, respectively. Antipsychotic agent[1]. | ||||||||||||
| Name | Eticlopride hydrochloride | ||||||||||||
| CAS | 97612-24-3 | ||||||||||||
| Formula | C17H26Cl2N2O3 | ||||||||||||
| Molar Mass | 377.31 | ||||||||||||
| Appearance | Solid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
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| Reference | [1]. Jennifer L Martelle, et al. A review of the discovery, pharmacological characterization, and behavioral effects of the dopamine D2-like receptor antagonist eticlopride. CNS Neurosci Ther. Fall 2008;14(3):248-62. |
Eticlopride hydrochloride
CAS: 97612-24-3 F: C17H26Cl2N2O3 W: 377.31
Eticlopride hydrochloride, a selective dopamine D2‐like receptor antagonist, exhibits high affinity for dopamine D2, α
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