Brilaroxazine (RP5603) is a potent and orally active multimodal dopamine (DA)/serotonin (5-HT) modulator. Brilaroxazine is a partial agonist of dopamine (DA) D2, D3, and D4 receptors, 5-HT1A (K i =1.5 nM) and 5-HT2A (K i =2.5 nM), and has antagonist activity at 5-HT2B (K i =0.19 nM), and 5-HT7 (K i =2.7 nM) receptors. Brilaroxazine is an atypical antipsychotic agent, and has the potential to improve cognitive impairments in neuropsychiatric and neurological diseases in vivo.
性状
Solid
IC50 & Target[1][2]
5-HT1A Receptor 1.5 nM (Ki) 5-HT2A Receptor
体内研究(In Vivo)
Brilaroxazine (oral gavage; 10 mg/kg; twice daily; 28 days) limits the functional and structural effects of pulmonary arterial hypertension (PAH), with significant improvements in pulmonary hemodynamics, right ventricular (RV) hypertrophy, SO2, and pulmonary blood vessel structural changes. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
ClinicalTrial
参考文献
[1]. Reviva Pharmaceuticals Reports RP5063 Positive Efficacy Results for Memory Deficits[2]. Bhat L, et al. Evaluation of the effects of RP5063, a novel, multimodal, serotonin receptor modulator, as single-agent therapy and co-administrated with sildenafil, bosentan, and treprostinil in a monocrotaline-induced pulmonary arterial hypertension rat
溶解度数据
In Vitro: DMSO : 100 mg/mL (222.04 mM; Need ultrasonic)配制储备液