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/ Clomipramine HCl/盐酸氯米帕明

Clomipramine HCl/盐酸氯米帕明 {[allProObj[0].p_purity_real_show]}

货号：A129557 同义名： 氯丙咪嗪盐酸盐 / Chlorimipramine hydrochloride; NSC-169865 hydrochloride

Clomipramine HCl是一种二苯并氮杂萘类衍生物的5-HT再摄取抑制剂，也是三环类抗抑郁药。

Clomipramine HCl/盐酸氯米帕明 化学结构 CAS号：17321-77-6
Clomipramine HCl/盐酸氯米帕明 化学结构
CAS号：17321-77-6
Clomipramine HCl/盐酸氯米帕明 3D分子结构
CAS号：17321-77-6
Clomipramine HCl/盐酸氯米帕明 化学结构 CAS号：17321-77-6
Clomipramine HCl/盐酸氯米帕明 3D分子结构 CAS号：17321-77-6
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Clomipramine HCl/盐酸氯米帕明 纯度/质量文件 产品仅供科研

货号：A129557 标准纯度： {[allProObj[0].p_purity_real_show]}
批次查询： 批次纯度:

全球学术期刊中引用的产品

• Nature, 2025, 645, 793-800. Ambeed. [ A201204 , A444152 , A344107 , A952055 ]
• Cell, 2025. Ambeed. [ A122167 ]
• Science, 2025, 387(6729): eadp5637. Ambeed. [ A875019 ]
• Sig. Transduct. Target. Ther., 2025, 10, 257. Ambeed. [ A104916 ]
• Nat. Nanotechnol., 2025. Ambeed. [ A243018 , A1216705 , A522597 , A125401 , A1355641 ]
更多 >
产品名称 5-HT ↓ 5-HT1 ↓ 5-HT2 ↓ 5-HT3 ↓ 5-HT5 ↓ 5-HT6 ↓ 5-HT7 ↓ 其他靶点 纯度
Desvenlafaxine ++

5-HT, Ki: 40.2 nM

 		98%
Lamotrigine +

5-HT (rat brain synaptosomes), IC50: 474 μM

5-HT (human platelets), IC50: 240 μM

 		98%
Venlafaxine ✔ 99%
Fluvoxamine maleate ✔ 99%
Iloperidone ✔ 99%
Ziprasidone HCl ✔ 98+%
Atomoxetine HCI +

5-HT, Ki: 77 nM

 		98%
Dapoxetine HCl ✔ 97%
Trazodone ✔ 98+%
Clomipramine HCl ✔ 98%
Mirtazapine ✔ 99+%
Escitalopram oxalate +++

5-HT, Ki: 0.89 nM

 		97%
Duloxetine ✔ 97%
Sertraline HCl ++

5-HT, Ki: 13 nM

 		98%
Citalopram HBr +++

serotonin reuptake, IC50: 1.8 nM

 		98%
Latrepirdine 2HCl ✔ GluR 99%
Fluoxetine HCl ✔ 99.5%
Paroxetine HCl ✔ AChR 99%
BMY 7378 ++

5-HT1A, pIC50: 6.4

5-HT1D, pIC50: 5.9

 		+

5-HT2, pIC50: 5.5

 		97%
Flibanserin +++

5-HT1A, Ki: 1 nM

 		+

5-HT2A, Ki: 49 nM

 		95%
LY310762 +

5-HT1D, Ki: 249 nM

 		99%+
Cyclobenzaprine HCI ✔ 99%
Blonanserin +++

5-HT2, Ki: 3.98 nM

 		99%
Cyproheptadine HCl ++++

5-HT2, IC50: 0.6 nM

 		99+%
Olanzapine ✔ 99+%
Pimavanserin hemitartrate +++

5-HT2A, pIC50: 8.7

 		99%
Ketanserin +++

5-HT2C (Human), Ki: 2.5 nM

5-HT2C (Rat), Ki: 50 nM

 		99%+
Loxapine succinate ++

5-HT2 (human), Ki: 6.8 nM

5-HT2 (bovine), Ki: 6.6 nM

 		98%
Agomelatine ✔ 98%
Clozapine ✔ 98%
Amitriptyline +

5-HT2, Ki: 235 nM

 		SERT 99%
PRX-08066 maleate +++

5-HT2B, IC50: 3.4 nM

 		98+%
RS-127445 ++++

5-HT2B, pIC50: 10.4

5-HT2B, pKi: 9.5

 		99%+
Sarpogrelate HCl ++++

5-HT2C, Kd: 1.1 nM

5-HT2A, Kd: 2.1 nM

 		98%
Tropisetron ✔ 99%
Ramosetron HCl ++++

5-HT3 receptor, Ki: 0.091 nM

 		98%
Ondansetron ✔ 99%
Granisetron ✔ 98%
Alosetron HCl ✔ 98%
Ondansetron HCl dihydrate ✔ 98%
VUF10166 ++++

5-HT3A, Ki: 0.04 nM

5-HT3AB, Ki: 22 nM

 		99%+
Azasetron HCl ++++

5-HT3, IC50: 0.33 nM

 		99%
Asenapine maleate +++

5-HT1B, pKi: 8.4

5-HT1A, pKi: 8.6

 		++++

5-HT2A, pKi: 9.75

5-HT2C, pKi: 10.46

 		+++

5-HT5A, pKi: 8.84

 		++++

5-HT6, pKi: 9.6

 		++++

5-HT7, pKi: 9.94

 		97%
Risperidone ++

5-HT1D, Ki: 84.6 nM

5-HT1B, Ki: 14.9 nM

 		++++

5-HT2A, Ki: 61.9 nM

5-HT2C, Ki: 12 nM

 		+

5-HT5A, Ki: 206 nM

 		++

5-HT7, Ki: 6.6 nM

 		98%
SB 271046 HCl +++

5-HT6, pKi: 8.92

 		99%+
Intepirdine ++++

5-HT6, pKi: 9.63

 		99%+
SB-269970 HCl ++

5-HT7, pKi: 8.3

 		98+%
BRL 15572 ++

5-HT1D, pKi: 6

5-HT1B, pKi: 6.1

 		++

5-HT2A, pKi: 6.6

5-HT2B, pKi: 6.2

 		+

5-HT6, pKi: 5.9

 		+

5-HT7, pKi: 6.3

 		95%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多，抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用，但抑制强度暂时没有相关数据。

Clomipramine HCl/盐酸氯米帕明 生物活性

靶点

  • 5-HT
描述 Clomipramine Hydrochloride is monoamine reuptake inhibitor and tricyclic antidepressant[3]. Preclinical studies in rodents indicated that clomipramine negatively affects hippocampus-dependent spatial learning and memory and clomipramine treatment reduced neuronal autophagic flux in primary dissociated neurons[4]. Clomipramine was inactive alone but produced a proportion-dependent enhancement of the antinociceptive effects of nalbuphine > morphine > methadone[5].

Clomipramine HCl/盐酸氯米帕明 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Sprague-Dawley (SD) rats Chronic unpredictable mild stress (CMS)-induced depression model Intraperitoneal injection 5 mg/kg Once daily for 4 weeks Clomipramine treatment significantly ameliorated CMS-induced depressive- and anxiety-like behaviors, reduced hippocampal neuroinflammation, and increased hippocampal volume. Transl Psychiatry. 2022 Jun 10;12(1):245
Rat Anesthetized rat lacrimal gland secretion model Intravenous injection 2 and 5 mg/kg Single dose To study the effects of acute administration on lacrimal gland secretion, results showed that Clomipramine significantly attenuated both reflex-evoked and methacholine-induced tear production. Invest Ophthalmol Vis Sci. 2021 Jun 1;62(7):8

Clomipramine HCl/盐酸氯米帕明 参考文献

[1]Ortiz J, Artigas F. Effects of monoamine uptake inhibitors on extracellular and platelet 5-hydroxytryptamine in rat blood: different effects of clomipramine and fluoxetine. Br J Pharmacol. 1992 Apr;105(4):941-6.

[2]McTavish D, Benfield P. Clomipramine. An overview of its pharmacological properties and a review of its therapeutic use in obsessive compulsive disorder and panic disorder. Drugs. 1990 Jan;39(1):136-53.

[3]Polonini HC, Silva SL, de Almeida TR, Brandão MAF, Ferreira AO. Compatibility of caffeine, carvedilol, clomipramine hydrochloride, folic acid, hydrochlorothiazide, loperamide hydrochloride, methotrexate, nadolol, naltrexone hydrochloride and pentoxifylline in SyrSpend SF PH4 oral suspensions. Eur J Hosp Pharm. 2016 Nov;23(6):352-358. doi: 10.1136/ejhpharm-2016-000903. Epub 2016 Mar 24. PMID: 31156882; PMCID: PMC6451465.

[4]Cavaliere F, Fornarelli A, Bertan F, Russo R, Marsal-Cots A, Morrone LA, Adornetto A, Corasaniti MT, Bano D, Bagetta G, Nicotera P. The tricyclic antidepressant clomipramine inhibits neuronal autophagic flux. Sci Rep. 2019 Mar 19;9(1):4881. doi: 10.1038/s41598-019-40887-x. PMID: 30890728; PMCID: PMC6424961.

[5]Banks ML, Rice KC, Negus SS. Antinociceptive interactions between Mu-opioid receptor agonists and the serotonin uptake inhibitor clomipramine in rhesus monkeys: role of Mu agonist efficacy. J Pharmacol Exp Ther. 2010 Nov;335(2):497-505. doi: 10.1124/jpet.110.169276. Epub 2010 Jul 30. PMID: 20675432; PMCID: PMC2967402.

Clomipramine HCl/盐酸氯米帕明 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.85mL

0.57mL

0.28mL

14.23mL

2.85mL

1.42mL

28.46mL

5.69mL

2.85mL

Clomipramine HCl/盐酸氯米帕明 技术信息

CAS号17321-77-6
分子式C19H24Cl2N2
分子量 351.31
SMILES Code CN(C)CCCN1C2=CC(Cl)=CC=C2CCC3=C1C=CC=C3.Cl
MDL No. MFCD00069234
别名 氯丙咪嗪盐酸盐 ;Chlorimipramine hydrochloride; NSC-169865 hydrochloride; Clomipramine (hydrochloride); Anafranil; G-34586 hydrochloride; Clomipramine hydrochloride
运输蓝冰
InChI Key WIMWMKZEIBHDTH-UHFFFAOYSA-N
Pubchem ID 68539
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry,2-8°C
溶解方案

DMSO: 50 mg/mL(142.32 mM)，配合低频超声助溶，注意：DMSO长时间开封后，会吸水并导致溶解能力下降，请避免使用长期开封的DMSO

H2O: 50 mg/mL(142.32 mM)

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液，再依次添加助溶剂：
——为保证实验结果的可靠性，澄清的储备液可以根据储存条件，适当保存；体内实验的工作液，建议现用现配，当天使用； 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比；如在配制过程中出现沉淀、析出现象，可以通过加热和/或超声的方式助溶
方案 一
方案 二
方案 三
配制的工作液建议现用现配，短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比；如在配制过程中出现沉淀、析出现象，可以通过加热和/或超声的方式助溶。
方案 一

Tags: Clomipramine | 17321-77-6 | Chlorimipramine | G-34586 | NSC-169865 | G34586 | G 34586 | NSC169865 | NSC 169865 | 5-HT Reuptake Inhibitor | Neuronal Signaling | Serotonin Transporter | 仅供科研使用 | AmBeed-信号通路专用抑制剂 | Clomipramine HCl/盐酸氯米帕明 纯度/质量文件 | Clomipramine HCl/盐酸氯米帕明 亚型比较 | Clomipramine HCl/盐酸氯米帕明 生物活性 | Clomipramine HCl/盐酸氯米帕明 参考文献 | Clomipramine HCl/盐酸氯米帕明 实验方案 | Clomipramine HCl/盐酸氯米帕明 技术信息

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