CAS NO: | 155270-99-8 |
生物活性 | Istradefylline is a very potent, selective and orally activeadenosine A2A receptorantagonist withKiof 2.2 nM in experimental models of Parkinson's disease. | ||||||||||||||||
IC50& Target | Ki: 2.2 nM (adenosine A2A receptor) | ||||||||||||||||
体外研究 (In Vitro) | Istradefylline has 70-fold greater affinity for the A2AR than the A1 receptor with Kiof 2.2 nM versus 150 nM[1]. Istradefylline causes concentration-dependent abolition of bFGF induction of astrogliosis in primary rat striatal astrocytes[4]. Istradefylline binds to A1 receptor, A2A receptor, and A3 receptor in human with Kis of >287 nM, 9.12 nM, and >681 nM, respectively, 50.9 nM and 1.57 nM for A1 receptor and A2A receptor in rat, 105.02 nM and 1.87 nM for A1 receptor and A2A receptor in mouse, respectively[5]. | ||||||||||||||||
体内研究 (In Vivo) | Istradefylline (3.3 mg/kg, i.p.) treatment before a single dose of MPTP attenuates the partial dopamine and DOPAC depletions measured in striata 1 week later[1]. Istradefylline reverses CGS21680-induced and reserpine-induced catalepsy with an ED50of 0.05 mg/kg and 0.26 mg/kg, respectively. Istradefylline is over 10 times as potent in these models compared to other adenosine antagonists and dopamine agonist drugs. Istradefylline combined with L-dopa cuases potent effects on haloperidol-induced and reserpine-induced catalepsy[2]. Istradefylline (10 mg/kg, p.o.) results an increase in locomotor activity to approximately twice that of control and improves motor disability in MPTP-treated common marmosets. Istradefylline (10 mg/kg, p.o.) in combination with SKF80723, quinpirole, or L-DOPA produces a significant additive effect on locomotor activity and improvement of motor disability but not dysKinesia[3]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 384.43 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H24N4O4 | ||||||||||||||||
CAS 号 | 155270-99-8 | ||||||||||||||||
中文名称 | 伊曲茶碱 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 25.33 mg/mL(65.89 mM;Need ultrasonic and warming) 配制储备液
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