化合物Dibenamine hydrochloride T37906
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
500 mg | 55-43-6 | ¥145.00 | 询底价 |
1 mL | 55-43-6 | ¥217.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Dibenamine hydrochloride
描述: Dibenamine hydrochloride 是竞争性的、不可逆的肾上腺素能阻断剂,可以修饰肾上腺素的药理作用。它对小鼠体内肾上腺素的破坏率显著增加。
体外活性: The irreversible inhibitory effects of dibenamine on the noradrenaline-, K- and Ba-induced contractions of rat's isolated vas deferens, particularly in relation to Ca.
体内活性: Dibenamine hydrochloride causes a significant increase in the rate of destruction of L-epinephrine in the mouse. Pretreatment with Dibenamine hydrochloride apparently slowed the conversion of Ccl4 to CHCL3. Dibenamine hydrochloride (25 mg/kg; s.c.) decreased the CHCl3, levels at 2 and 6 hr by 30%-50%[3].
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 125 mg/mL (421.97 mM)
H2O : 33.33 mg/mL (112.51 mM)
关键字: Adrenergic Receptor | Acetylcholine | Inhibitor | inhibit | Dibenamine | adrenergic | epinephrine | Dibenamine hydrochloride | hepatotoxicity | Dibenamine Hydrochloride | Beta Receptor
相关产品: Piperoxan hydrochloride | Pardoprunox hydrochloride | ICI 118,551 hydrochloride | Zotepine | Quetiapine | D2343 | Benzquinamide | Trazodone hydrochloride | G-Protein antagonist peptide acetate | Clonidine hydrochloride
相关库: Neurotransmitter Receptor Compound Library | Anti-Cancer Compound Library | Membrane Protein-targeted Compound Library | Bioactive Compounds Library Max | Neuronal Signaling Compound Library | GPCR Compound Library | Inhibitor Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途