Clomipramine HCl |
| Catalog No.GC15107 |
Le chlorhydrate de clomipramine (Chlorimipramine) est un puissant bloqueur de la recapture de la 5-HT avec une valeur IC50 de 1,5 nM.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 17321-77-6
Sample solution is provided at 25 µL, 10mM.
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Clomipramine hydrochloride is a serotonin transporter (SERT), norepinephrine transporter (NET) and dopamine transporter (DAT) blocker with Ki of 0.14, 54 and 3 nM, respectively.
Clomipramine hydrochloride is a hydrochloride salt of clomipramine which is a serotonin transporter (SERT), norepinephrine transporter (NET) dopamine transporter (DAT) blocker with Ki of 0.14, 54 and 3 nM, respectively. Clomipramine hydrochloride (Anafranil) is a tricyclic antidepressant. Clomipramine hydrochloride is a norepinephrine-reuptake inhibitor and is an antiobsessional drug. Clomipramine hydrochloride is an antagonist/inverse agonist at the following receptors: D2 receptor (Ki=162 nM), D3 receptor (Ki=30 nM), α1-adrenergic receptor (Ki=3.2 nM), α2-adrenergic receptor (Ki=525 nM), H1 receptor (Ki=31 nM), mACh receptors (Ki=37 nM), 5-HT2A receptor (Ki=36 nM), 5-HT2C receptor (Ki=65 nM), 5-HT3 receptor (Ki=85 nM), 5-HT6 receptor (Ki=54 nM), 5-HT7 receptor (Ki=127 nM), D1 receptor (Ki=219 nM)[1][2][3].
References:
[1]. McTavish, D. and P. Benfield, Clomipramine. An overview of its pharmacological properties and a review of its therapeutic use in obsessive compulsive disorder and panic disorder. Drugs, 1990. 39(1): p. 136-53.
[2]. Ortiz, J. and F. Artigas, Effects of monoamine uptake inhibitors on extracellular and platelet 5-hydroxytryptamine in rat blood: different effects of clomipramine and fluoxetine. Br J Pharmacol, 1992. 105(4): p. 941-6.
[3]. Owens, M.J., et al., Neurotransmitter receptor and transporter binding profile of antidepressants and their metabolites. J Pharmacol Exp Ther, 1997. 283(3): p. 1305-22.
| Cas No. | 17321-77-6 | SDF | |
| Chemical Name | 3-(2-chloro-5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N,N-dimethylpropan-1-amine;hydrochloride | ||
| Canonical SMILES | CN(C)CCCN1C2=CC=CC=C2CCC3=C1C=C(C=C3)Cl.Cl | ||
| Formula | C19H23ClN2.HCl | M.Wt | 351.31 |
| Solubility | ≥ 17.6mg/mL in DMSO | Storage | Store at RT |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
|
1 mg | 5 mg | 10 mg |
| 1 mM | 2.8465 mL | 14.2324 mL | 28.4649 mL |
| 5 mM | 0.5693 mL | 2.8465 mL | 5.693 mL |
| 10 mM | 0.2846 mL | 1.4232 mL | 2.8465 mL |
Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
g
μL
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.
Quality Control & SDS
- View current batch:
- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5 (Based on Reviews and 39 reference(s) in Google Scholar.)
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