USP5-Cav3.2 inhibitor II-1 | USP5-Cav3.2 inhibitor | Probechem Biochemicals

首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Calcium Channel -USP5-Cav3.2 inhibitor II-1

Chemical Structure : USP5-Cav3.2 inhibitor II-1

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USP5-Cav3.2 inhibitor II-1 (Compound II-1)

货号: PC-72884Not For Human Use, Lab Use Only.

USP5-Cav3.2 inhibitor II-1 is a small molecule inhibitor of USP5-Cav3.2 interaction, without affecting the enzymatic activity of USP5.

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

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

USP5-Cav3.2 inhibitor II-1 is a small molecule inhibitor of USP5-Cav3.2 interaction, without affecting the enzymatic activity of USP5.
II-1 inhibited both phases of formalin-induced nocifensive behaviors in mice.
Cav3.2 is required for the action of II-1.
II-1 also mediated a robust inhibition of mechanical allodynia induced by injury to the sciatic nerve.

物理化学性质&存储条件

分子量	264.31
分子式	C8H12N2O4S2
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	3-hydroxy-2-(((4-oxo-2-thioxothiazolidin-5-yl)methyl)amino)butanoic acid

参考文献

1. Garcia-Caballero A, et al. ACS Chem Neurosci. 2022 Feb 16;13(4):524-536.

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USP5-Cav3.2 inhibitor II-1 (Compound II-1)

生物&药学活性

物理化学性质&存储条件

参考文献

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USP5-Cav3.2 inhibitor II-1 (Compound II-1)

生物&药学活性

物理化学性质&存储条件

参考文献

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