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Amisulpride Hydrochloride ndopril Smiles: C[C@@H]1C[C@@H]2CC[C@@H]3O[C@H](CC3=C)CC[C@@]34C[C@H]5O[C@H]6[C@@H](O3)[C@H]3O[C@@H](CC(=O)C[C@@H]7[C@@H](OC)[C@@H](C[C@H](O)CN)O[C@H]7C[C@@H](O2)C1=C)CC[C@@H]3O[C@H]6[C@H]5O4

SKU: 76163353068

4.2
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Amisulpride Hydrochloride ndopril Smiles: C[C@@H]1C[C@@H]2CC[C@@H]3O[C@H](CC3=C)CC[C@@]34C[C@H]5O[C@H]6[C@@H](O3)[C@H]3O[C@@H](CC(=O)C[C@@H]7[C@@H](OC)[C@@H](C[C@H](O)CN)O[C@H]7C[C@@H](O2)C1=C)CC[C@@H]3O[C@H]6[C@H]5O4Amisulpride is an atypical antipsychotic used to treat psychosis in schizophrenia and episodes of mania in bipolar disorder. In Italy, it is also used as a treatment for dysthymia. It was introduced by Sanofi Aventis in the 1990s. Its patent had expired by 2008 and hence generic formulations are now available. Amisulpride function primarily as a D2 and D3 receptor antagonist. It has high affinity for these receptors with dissociation constants of 2. 2

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Description

Smiles: C[C@@H]1C[C@@H]2CC[C@@H]3O[C@H](CC3=C)CC[C@@]34C[C@H]5O[C@H]6[C@@H](O3)[C@H]3O[C@@H](CC(=O)C[C@@H]7[C@@H](OC)[C@@H](C[C@H](O)CN)O[C@H]7C[C@@H](O2)C1=C)CC[C@@H]3O[C@H]6[C@H]5O4

Food and Drug Administration (FDA) in late May 2007

Mendiratta S

Smiles: CC(C)[C@H]1C(=O)N[C@@H](CC2=CNC3=CC=CC(=C23)N1C)CO

Amisulpride Hydrochloride ndopril Smiles: C[C@@H]1C[C@@H]2CC[C@@H]3O[C@H](CC3=C)CC[C@@]34C[C@H]5O[C@H]6[C@@H](O3)[C@H]3O[C@@H](CC(=O)C[C@@H]7[C@@H](OC)[C@@H](C[C@H](O)CN)O[C@H]7C[C@@H](O2)C1=C)CC[C@@H]3O[C@H]6[C@H]5O4Amisulpride is an atypical antipsychotic used to treat psychosis in schizophrenia and episodes of mania in bipolar disorder. In Italy, it is also used as a treatment for dysthymia. It was introduced by Sanofi Aventis in the 1990s. Its patent had expired by 2008 and hence generic formulations are now available. Amisulpride function primarily as a D2 and D3 receptor antagonist. It has high affinity for these receptors with dissociation constants of 2. 2

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