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- 详细信息
- 文献和实验
- 技术资料
- CAS号:
1225-55-4
- 规格:
1mLx10mM(inDMSO)/1mg/5mg/10mg
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥233.0 |
|---|---|---|---|
| 规格: | 1mg | 产品价格: | ¥111.0 |
| 规格: | 5mg | 产品价格: | ¥213.0 |
| 规格: | 10mg | 产品价格: | ¥330.0 |
Product Introduction
Bioactivity
| 名称 | Protriptyline hydrochloride |
| 描述 | Protriptyline Hydrochloride is the hydrochloride salt form of protriptyline, a tricyclic secondary amine with an antidepressant property. Protriptyline hydrochloride (Protriptyline HCl) blocks the re-uptake of norepinephrine and serotonin by nerve terminals, thereby increasing available norepinephrine and serotonin. In addition, this agent exhibits anticholinergic activity. |
| 存储条件 | Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (6.67 mM), Sonication is recommended. 10% DMSO+90% Saline : 10 mg/mL (33.35 mM), Solution. DMSO : 150 mg/mL (500.27 mM), Sonication is recommended. |
| 关键字 | Sert (Sodium-dependent) | Protriptyline hydrochloride | Protriptyline | Inhibitor | inhibit | Cholinesterase (ChE) | Aβ Self-Assembly | alzheimers | AChE | 5HTReceptor | 5HT Receptor |
| 相关产品 | Cefaclor monohydrate | 2,4-Di-tert-butylphenol | Cinchonidine | 10-Undecenoic acid | Coumaran | Alverine citrate | Diethyltoluamide | Dapoxetine hydrochloride | HEPPS | Dimethyl sulfoxide | Uridine 5'-monophosphate disodium salt | 1,8-Cineole |
| 相关库 | Bioactive Compound Library | Anti-Cancer Approved Drug Library | Bioactive Compounds Library Max | Approved Drug Library | Serotonin Receptor-Targeted Compound Library | FDA-Approved Drug Library | GPCR Compound Library | Membrane Protein-targeted Compound Library | Anti-Neurodegenerative Disease Compound Library | Drug Repurposing Compound Library | Pain-Related Compound Library | Anti-Cancer Drug Library |
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文献和实验动物种始发情期 (生后)(日)繁殖适龄期 (生后)成熟体重性周期(日)发情持续 时间(小时)发情性质由发情开始至排卵妊娠期(日)产仔数新生体重(g)哺乳时间离乳体重(g)成年体重(g)小鼠30-408周20g以上5(4-7)12(8-20)全年2-3小时19(18-20)6(1-18)1.521日10-1225-30大鼠50-603月♂250g以上 ♀150g以上4(4-5)13.5(8-20)全年8-10小时20(19-22)8(1-12)5-621日35-40250-400豚鼠45-604
成分 绞碎猪胃 100g 绞碎猪血块 100g 蒸馏水 1000mL 浓盐酸 10mL 制法 1 洗涤猪胃,除去油脂,保留胃粘膜,用绞肉机绞碎。 2 用绞肉机将猪血块绞碎。 3 将蒸馏水加热至55℃,加入猪胃、猪血块和盐酸,置55℃水浴中24h,时常加以摇动。 4 从水浴内取出,加入1moL/L碳酸钠溶液5mL,煮沸10min,置于冰箱内一夜。 5
作用与抗炎作用密切相关。本实验通过热刺激致痛模型,比较了吗啡及水杨酸钠镇痛作用机制的差异。 【实验对象】 小鼠(昆明种),体重20g左右,雌性。 【试剂与器材】 0.1%盐酸吗啡溶液,4%盐酸水杨酸钠(乙酰水杨酸)溶液,苦味酸,生理盐水,电热板,注射器,天平。 【实验方法与步骤】 1. 筛选小鼠 将小鼠置于温度55℃±0.5℃的金属热板上,测定其疼痛反应(“舔后足”现象)的出现时间,共测定2次,每次间隔5min。若出现疼痛反应的时间在10
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