ZK756326 dihydrochloride
目录号: PL01166 纯度: ≥99%
CAS No. :1780259-94-0
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中文名称
ZK756326 dihydrochloride
中文别名
ZK756326(dihydrochloride)
英文名称
ZK756326 dihydrochloride
英文别名
ZK756326(dihydrochloride);ZK756326 dihydrochloride;ZK756326 2HCl;ZK 756326;ZK756326 (dihydrochloride);ZK756326;2-[2-[4-[(3-phenoxyphenyl)methyl]-1-piperazinyl]ethoxy]ethanol dihydrochloride;ZK 756326 dihydrochloride;zk 756326 2HCl;BCP29859;ZJB91196;s8324;B7109;A16363;2-[2-[4-[(3-phenoxyphenyl)methyl]piperazin-1-yl]ethoxy]ethanol;dihydrochloride
Cas No.
1780259-94-0
分子式
C21H30Cl2N2O3
分子量
429.38
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
ZK756326 dihydrochloride 是一种非肽趋化因子受体激动剂,作用于 CC 趋化因子受体 CCR8。
生物活性
ZK756326 dihydrochloride is a nonpeptide chemokine receptor agonist for the CC chemokine receptor CCR8.
性状
Solid
IC50 & Target[1][2]
CCR8 1.8 μM (IC50, in U87 cells) 5-HT1A
体外研究(In Vitro)
ZK 756326 inhibits the binding of the CCR8 ligand I-309 (CCL1), with an IC50 value of 1.8 μM. ZK 756326 is a full agonist of CCR8, dose-responsively eliciting an increase in intracellular calcium and cross-desensitizing the response of the receptor to CCL1. ZK 756326 stimulates extracellular acidification in cells expressing human CCR8. Binding competition assays are performed on a series of other G-protein-coupled receptors to determine whether the interaction of ZK 756326 is specific for CCR8. In these assays, ZK 756326 is tested at 50 μM for inhibition of radiolabeled ligand binding. At this concentration, ZK 756326 shows >28 fold specificity for CCR8 compared with 26 other GPCRs, all with IC50 values of >50 μM. There is less selectivity when ZK 756326 is tested against the serotonergic receptors 5-HT1A, 5-HT2B, 5-HT2C
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Haskell CA, et al. Identification and characterization of a potent, selective nonpeptide agonist of the CC chemokine receptor CCR8. Mol Pharmacol. 2006 Jan;69(1):309-16.
溶解度数据
In Vitro: H2O : 50 mg/mL (116.45 mM; Need ultrasonic)DMSO : 27.5 mg/mL (64.05 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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