Diphenylpyraline (Synonyms: 二苯拉林; 双苯拉林)
目录号: PL14957 纯度: ≥99%
CAS No. :147-20-6
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中文名称
Diphenylpyraline
中文别名
双苯拉林;4-(二苯基甲氧基)-1-甲基哌啶;二苯拉林;双苯拉林 标准品
英文名称
Diphenylpyraline
英文别名
diphenylpyraline;4-(diphenylmethoxy)-1-methylpiperidine;4-benzhydryloxy-1-methylpiperidine;DIPHENYLPYRALINE , CRM STANDARD;Piperidine,4-(diphenylmethoxy)-1-methyl-;4-Benzhydryloxy-1-methyl-piperidin;4-benzhydryloxy-1-methyl-piperidine;4-Diphenylmethoxy-1-methyl-piperidin;Allergen;Belfene;Dayfen;Hispril;Histyn;Lergobine;Lyssipoll;Mepiben;Neargal;N-methyl-4-(diphenylmethoxy)piperidine;P-253;Hystryl;Aids033087;Aids-033087;Nsc61825 (HCl);132-18-3 (Hcl);Diphenylpyraline
Cas No.
147-20-6
分子式
C19H23NO
分子量
281.39
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Diphenylpyraline 是一种有效的组胺 H1 受体 (histamine H1 receptor) 的拮抗剂。Diphenylpyraline 是一种具有口服活性抗组胺试剂,具有抗胆碱和抗过敏作用。Diphenylpyraline 可用于过敏性疾病,包括鼻炎和花粉热,以及瘙痒性皮肤疾病等的研究。
生物活性
Diphenylpyraline is a potent histamine H 1  receptor antagonist. Diphenylpyraline acts as an orally active antihistamine agent with antimuscarinic and antiallergic effects. Diphenylpyraline can be used for the research of allergic diseases, including rhinitis and hay fever, and pruritic skin disorders et.al.
性状
Solid
IC50 & Target[1][2]
H1 Receptor
体外研究(In Vitro)
Diphenylpyraline (10 μM) markedly inhibits dopamine uptakein mouse nucleus accumbens slices. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Diphenylpyraline (intraperitoneal injection; 5-10 mg/kg) elevates extracellular dopamine levels (~200%) in mouse nucleus accumbens and induces locomotor activation in mice. 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
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Erik B Oleson, et al. Effects of the histamine H? receptor antagonist and benztropine analog diphenylpyraline on dopamine uptake, locomotion and reward.
[2]. Gennady B Lapa, et al. Diphenylpyraline, a histamine H1 receptor antagonist, has psychostimulant properties.
溶解度数据
In Vitro: DMSO : 100 mg/mL (355.38 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)配制储备液
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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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