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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Calcium Channel -Z-944
Z-944

Chemical Structure : Z-944

CAS No.: 1199236-64-0

Z-944 (Ulixacaltamide, Z944)

货号: PC-62009Not For Human Use, Lab Use Only.

Z-944 (Ulixacaltamide) is a potent, highly selective and oral T-type calcium channel blocker with IC50 of 50-160 nM for human Cav3.1, Cav3.2, and Cav3.3 channels.

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

生物&药学活性

Z-944 (Ulixacaltamide) is a potent, highly selective and oral T-type calcium channel blocker with IC50 of 50-160 nM for human Cav3.1, Cav3.2, and Cav3.3 channels.
Z-944 (Ulixacaltamide) displays 70 times more potent for T-type blockade than for blockade of the N-type channel (IC50=11 uM).
Z-944 (Ulixacaltamide) potently suppress seizure activity and attenuates burst firing of thalamic reticular nucleus neurons in the GAERS model of absence epilepsy.
Z-944 (Ulixacaltamide) restores cortical synchrony and thalamocortical connectivity in a rat model of neuropathic pain.

物理化学性质&存储条件

分子量 383.89
分子式 C19H27ClFN3O2
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

N-[[1-[2-(tert-butylamino)-2-oxoethyl]piperidin-4-yl]methyl]-3-chloro-5-fluorobenzamide

参考文献

1. Tringham E, et al. Sci Transl Med. 2012 Feb 15;4(121):121ra19.

2. Casillas-Espinosa PM, et al. PLoS One. 2015 Aug 14;10(8):e0130012.

3. LeBlanc BW, et al. Pain. 2016 Jan;157(1):255-63.

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