Fluphenazine-N-2-chloroethane (hydrochloride)

 化学構造式
3892-78-2
CAS番号.
3892-78-2
化学名:
别名:
英語名:
Fluphenazine-N-2-chloroethane (hydrochloride)
英語别名:
10-[3-[4-(2-chloroethyl)-1-piperazinyl]propyl]-2-(trifluoromethyl)-10H-phenothiazinedihydrochloride
CBNumber:
CB03152614
化学式:
C22H26Cl2F3N3S
分子量:
492.4281496
MOL File:
3892-78-2.mol

Fluphenazine-N-2-chloroethane (hydrochloride) 物理性質

融点 :
224-225 °C
貯蔵温度 :
Store at -20°C
溶解性:
DMF: 10 mg/ml; DMSO: 10 mg/ml; Ethanol: 1 mg/ml
外見 :
A crystalline solid

安全性情報

Fluphenazine-N-2-chloroethane (hydrochloride) 価格

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入

Fluphenazine-N-2-chloroethane (hydrochloride) 化学特性,用途語,生産方法

説明

Fluphenazine is a traditional antipsychotic compound that tightly binds the dopamine D2 receptor (Ki = 0.55 nM) and also reversibly inhibits calmodulin at micromolar concentrations. Fluphenazine-N-2-chloroethane is a derivative of fluphenazine that contains an alkylating chlorethylamine chain, which produces irreversible protein binding. It is a relatively selective, irreversible antagonist of D2 receptors both in vitro (IC50 = 100 nM) and in vivo, inactivating approximately 90% of D2 receptors in mice within 4 hours of treatment. Through this action, fluphenazine-B-2-chloroethane can be used to induce catalepsy in mice. It irreversibly inhibits calmodulin at higher doses (IC50 = 10 μM), which can sensitize cancer cells to TRAIL-induced apoptosis.

使用

Fluphenazine is a traditional antipsychotic compound that tightly binds the dopamine D2 receptor (Ki = 0.55 nM) and also reversibly inhibits calmodulin at micromolar concentrations. Fluphenazine-N-2-chloroethane (hydrochloride) is a derivative of fluphenazine that contains an alkylating chlorethylamine chain, which produces irreversible protein binding. It is a relatively selective, irreversible antagonist of D2 receptors both in vitro (IC50 = 100 nM) and in vivo, inactivating approximately 90% of D2 receptors in mice within 4 hours of treatment. Through this action, fluphenazine-B-2-chloroethane can be used to induce catalepsy in mice. It irreversibly inhibits calmodulin at higher doses (IC50 = 10 μM), which can sensitize cancer cells to TRAIL-induced apoptosis.[Cayman Chemical]

Fluphenazine-N-2-chloroethane (hydrochloride) 上流と下流の製品情報

原材料

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Fluphenazine-N-2-chloroethane (hydrochloride) 生産企業

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