LZX-2-73

Chemical Structure : LZX-2-73

加入收藏

货号: PC-23558Not For Human Use, Lab Use Only.

LZX-2-73 is a specific and effective NUPR1 inhibitor with Kd of 2.7 uM, inhibits MIA PaCa-2 cell proliferation with IC50 of 10.9 uM.

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

LZX-2-73 is a specific and effective NUPR1 inhibitor with Kd of 2.7 uM, inhibits MIA PaCa-2 cell proliferation with IC50 of 10.9 uM.
LZX-2-73 is more efficient than AJO14 in vitro and in vivo.
5 or 25 mg/kg of LZX-2-73 showed slow tumor growth and a significantly reduced tumor volume compared to the control group in a dose-dependent manner.
LZX-2-73 does not bind to hERG, indicating no risk of cardiotoxicity.

物理化学性质&存储条件

分子量	427.33
分子式	C16H15BrN2O3S2
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-(3-bromophenyl)-3-(3-(methylsulfonyl)-6,7-dihydrobenzo[c]thiophen-1-yl)urea

参考文献

1. Liu X, et al. Sci Rep. 2024 Nov 27;14(1):29515.

LZX-2-73

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

LZX-2-73

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.