| CAS: | 1187020-80-9 | ||
| 分子式: | C31H36FN3O4S | ||
| 分子量: | 565.7 | ||
| 中文名称: |
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| 英文名称: |
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| 用途: | Lumateperone甲苯磺酸盐是5-HT 2A受体拮抗剂 (KI= 0.54 nM), 突触前D2受体的部分激动剂和突触后D2受体的拮抗剂 (KI= 32 nM)。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||||
| T884160 | MACKLIN | lumateperone Tosylate | ≥99% | 411元/5mg; 685元/10mg; 1165元/25mg; 1985元/50mg; 3367元/100mg; 5925元/250mg; | 展开 | ||||||||||||||||||||||||||||||||||||||||
储存:2-8℃ 状态:白色到灰色固体 | |||||||||||||||||||||||||||||||||||||||||||||
| SML2866 | Sigma-Aldrich | Lumateperone tosylate | ≥98% (HPLC) | 940.27元/10 MG; 3793.48元/50 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||
产品说明 生化/生理作用 Lumateperone tosylate (ITI-007) is an orally active, potent 5-HT2A antagonist, postsynaptic D2 antagonist, and serotonin transporter SERT inhibitor (Ki = 0.5, 32, 62 nM, respectively) with in vivo antipsychotic efficacy and no effect toward receptors associated with cognitive and metabolic side effects of antipsychotic drugs (e.g., H1, 5-HT2C, muscarinic). ITI-007 blocks DOI-induced headtwitch (ID50 = 0.09 mg/kg, po.) and D-AMPH-induced hyperlocomotion in mice (ID50 = 0.95 mg/kg, po.), while also acting as a partial agonist at presynaptic striatal D2 receptors. 基本信息
产品性质
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