IDPU

Chemical Structure : IDPU

加入收藏

货号: PC-26034Not For Human Use, Lab Use Only.

IDPU is a high potent, selective Adenosine A2A receptor (A2AR) antagonist with Ki of 0.0038 nM, has 737-fold selectivity over A1R.

规格	价格	库存	数量
50 mg		Get quote
100 mg		Get quote
250 mg		Get quote

获取报价单

* 请选择数量再加入购物车

or Bulk Inquiry

大包装，大折扣！

E-mail: sales@probechem.com

Tech Support: tech@probechem.com

生物&药学活性

IDPU is a high potent, selective Adenosine A2A receptor (A2AR) antagonist with Ki of 0.0038 nM, has 737-fold selectivity over A1R.
IDPU attenuates haloperidol induced Parkinson like symptoms in rats.
IDPU successfully restores hypo-locomotion induced by haloperidol and NECA.
IDPU also displays protective effect against oxidative stress induced by chronic haloperidol treatment in rats.

物理化学性质&存储条件

分子量	284.36
分子式	C9H12N6OS2
外观性状	Solid
CAS No.
储存条件	固体粉末 -20°C 12 个月; 4°C 6 个月	配置液 -80°C 6 个月; -20°C 6 个月
Shipping
Solubility	10 mM in DMSO
Chemical Name/SMILES	1-(7-imino-3-propyl-2-thioxo-3,7-dihydrothiazolo[4,5-d]pyrimidin-6(2H)-yl)urea

参考文献

1. Kumari N, et al. Neurosci Lett. 2017 Apr 24;647:53-60.

2. Kumari N, et al. Neurosci Lett. 2018 May 14;675:74-82.

3. Luthra PM, et al. Bioorg Med Chem Lett. 2010 Feb 1;20(3):1214-8.

IDPU

生物&药学活性

物理化学性质&存储条件

参考文献

Bulk Inquiry

* Indicates a Required FieldYour information is safe with us.

询单

IDPU

生物&药学活性

物理化学性质&存储条件

参考文献

Bulk Inquiry

* Indicates a Required FieldYour information is safe with us.

询单

Get Quotation Now

* Indicates a Required FieldYour information is safe with us.