Ocinaplon 是一种GABAA受体的阳性变构调节剂，在 α1 亚基处有较高的活性。

Ocinaplon is a GABAA receptors modulator.

In rats, ocinaplon produces significant muscle relaxation, ataxia, and sedation only at doses >25-fold higher than the minimum effective dose (3.1 mg/kg) in the Vogel "conflict" test[2].

96604-21-6

C17H11N5O

301.3

奥西普隆;DOV 273547

DMSO:<1 mgml
2eq.HCl:<25mg>Powder: -20°C for 3 years
In solvent: -80°C for 2 years