PRX-07034 hydrochloride
目录号: PL04104 纯度: ≥98%
PRX-07034 hydrochloride 是一种有效的高度选择性 5-HT6 受体拮抗剂,Ki 为 4-8 nM,IC50 为 19 nM。PRX-07034 可用于增强工作记忆和认知灵活性的研究。
CAS No. :903580-39-2
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中文名称
PRX-07034 hydrochloride
英文名称
PRX-07034 hydrochloride
英文别名
PRX 07034;PILCQJJJAFRKHO-UHFFFAOYSA-N;DB05993;Q27894078;N-[1-(5-chloro-2,3-dimethoxyphenyl)ethyl]-2-methanesulfonyl-5-(piperazin-1-yl)aniline hydrochloride;Benzenemethanamine, 5-chloro-2,3-dimethoxy-alpha-methyl-N-(2-(methylsulfonyl)-5-(1-piperazinyl)phenyl)-, hydrochloride (1:1);Benzenemethanamine, 5-?chloro-?2,?3-?dimethoxy-?;A-?methyl-?N-?[2-?(methylsulfonyl)?-?5-?(1-?piperazi;[1-(5-chloro-2,3-dimethoxy-phenyl)-ethyl]-(2;N-[1-(5-Chloro-2,3-dimethoxyphenyl)ethyl]-2-methylsulfonyl-5-piperazin-1-ylaniline;hydrochloride;Benzenemethanamine, 5-chloro-2,3-dimethoxy-α-methyl-N-[2-(methylsulfonyl)-5-(1-piperazinyl)phenyl]-, monohydrochloride (9CI)
Cas No.
903580-39-2
分子式
C21H29Cl2N3O4S
分子量
490.44
包装储存
-20°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
PRX-07034 hydrochloride 是一种有效的高度选择性 5-HT6 受体拮抗剂,Ki 为 4-8 nM,IC50 为 19 nM。PRX-07034 可用于增强工作记忆和认知灵活性的研究。
生物活性
PRX-07034 hydrochloride is a highly selective and potent 5-HT6 receptor antagonist with a K i = 4-8 nM and an IC 50 of 19 nM. PRX-07034 can be used for the research of enhancing working memory and cognitive flexibility.
性状
Solid
IC50 & Target[1][2]
5-HT6 Receptor 4-8 nM (Ki) 5-HT6 Receptor
体外研究(In Vitro)
PRX-07034 is both a potent and highly selective 5-HT6 receptor antagonist (≥100-fold selectivity for the 5-HT6 receptor compared to 68 other GPCRs, ion channels, and transporters. PRX-07034 inhibits 5-HT1A, 5-HT1B, 5-HT1D, Dopamine D3, Histamine H2, and Opioid μ receptor with Kis of 420 nM, 260 nM, 2.8 μM, 71 nM, 0.64 μM, and 0.45 μM, respectively. PRX-07034 inhibits 5-HT2A, 5-HT2B, and 5-HT2C receptors with IC50s of 2.5 μM, 2.5 μM, and 3.7 μM, respectively.
In functional assays, PRX-07034 demonstrates low antagonist activity for the dopamine D3 receptor (IC50=4.8 μM) and very low agonistic activity for the opioid μ-receptor (EC50=19 μM) . has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
PRX-07034 (0.1, 1, or 3 mg/kg; i.p.; 30 min prior to delayed spontaneous alternation testing) selectively enhances a switch to a place discrimination. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
-20°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]. Eric G Mohler, et al. The effects of PRX-07034, a novel 5-HT6 antagonist, on cognitive flexibility and working memory in rats. Psychopharmacology (Berl). 2012 Apr;220(4):687-96.
溶解度数据
In Vitro: DMSO : 31.25 mg/mL (63.72 mM; ultrasonic and warming and heat to 60°C)H2O : 4.76 mg/mL (9.71 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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