Odapipam (NNC 756) 是一种选择性，高亲和力的苯并氮杂卓多巴胺 D1 受体拮抗剂，Kd 为 0.18 nM。Odapipam 还是一种出色的正电子发射断层扫描 (PET) 放射性示踪剂。
| 生物活性 |
Odapipam (NNC 756) is a selective, high affinity and benzazepine dopamine D1 receptor antagonist with a Kd of 0.18 nM. Odapipam is also a superior positron emission tomography (PET) radiotracer. |
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| 体内研究 |
The metabolism of Odapipam has been studied with phenobarbital-induced rat liver microsomes. During the incubation of Odapipam, five different metabolites are formed. The electron-ionization (EI) mass spectra of the metabolites indicated the formation of N-desmethyl-Odapipam, 1-hydroxy-Odapipam, the two isomers of 3′-hydroxy-Odapipam and a metabolite which is dehydrogenated in the dihydrobenzofuran moiety.
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| 分子式 |
C19H20NO2Cl
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| 分子量 |
329.82
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| CAS号 |
131796-63-9
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| 运输条件 |
Room temperature in continental US; may vary elsewhere. |
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| 储存方式 |
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纯度： 98%
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