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Clomipramine

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Catalog No. T21013Cas No. 303-49-1
Alias Clomipramina, Clomicalm, Chlorimipramine, Anafranil (free base), Anafranil

Clomipramine (Clomicalm) is a tricyclic antidepressant (TCA). It is used for the treatment of the panic disorder, obsessive-compulsive disorder, major depressive disorder, and chronic pain. It may decrease the risk of suicide in those over the age of 65. It is similar to Imipramine in that selective inhibition of the serotonin uptake in the brain.

Clomipramine

Clomipramine

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Purity: 99.71%
Catalog No. T21013Alias Clomipramina, Clomicalm, Chlorimipramine, Anafranil (free base), AnafranilCas No. 303-49-1
Clomipramine (Clomicalm) is a tricyclic antidepressant (TCA). It is used for the treatment of the panic disorder, obsessive-compulsive disorder, major depressive disorder, and chronic pain. It may decrease the risk of suicide in those over the age of 65. It is similar to Imipramine in that selective inhibition of the serotonin uptake in the brain.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$31In StockIn Stock
25 mg$55In StockIn Stock
50 mg$89In StockIn Stock
100 mg$129In StockIn Stock
1 mL x 10 mM (in DMSO)$35In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.71%
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Product Introduction

Clomipramine AI Summary
Clomipramine exhibits a range of bioactivities, primarily involving the inhibition of neurotransmitter reuptake and various receptor bindings. It is notably potent in inhibiting norepinephrine (IC50 = 900 nM) and serotonin (IC50 = 90 nM) accumulation in mouse brain slices and exhibits antidepressant activity by inhibiting tetrabenazine (TBZ) ptosis and potentiating 5-hydroxytryptophan-induced head twitches in rats. Additionally, it demonstrates high affinity interactions with the dopamine D2, alpha-1 adrenergic, and serotonin receptors, with Ki values indicating significant binding strength, and shows inhibitory effects on multiple neurotransmitter transporters and voltage-dependent sodium channels. The compound also presents cytotoxicity and antitrypanosomal actions against Trypanosoma cruzi amastigotes, suggesting potential anti-parasitic applications. Long-term biological effects include a high volume of distribution, indicating extensive tissue penetration, and significant metabolic interactions with liver enzymes. Despite exhibiting some beneficial therapeutic activities, Clomipramine also has potential for neurotoxicity and hepatotoxicity, which necessitates careful consideration in therapeutic contexts..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Clomipramine (Clomicalm) is a tricyclic antidepressant (TCA). It is used for the treatment of the panic disorder, obsessive-compulsive disorder, major depressive disorder, and chronic pain. It may decrease the risk of suicide in those over the age of 65. It is similar to Imipramine in that selective inhibition of the serotonin uptake in the brain.
SynonymsClomipramina, Clomicalm, Chlorimipramine, Anafranil (free base), Anafranil
Chemical Properties
Molecular Weight314.85
FormulaC19H23ClN2
Cas No.303-49-1
SmilesCN(C)CCCN1c2ccccc2CCc2ccc(Cl)cc12
Relative Density.1.119 g/cm3
Storage & Solubility Information
Storagekeep away from moisture | Pure form: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 120 mg/mL (381.13 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.35 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1761 mL15.8806 mL31.7612 mL158.8058 mL
5 mM0.6352 mL3.1761 mL6.3522 mL31.7612 mL
10 mM0.3176 mL1.5881 mL3.1761 mL15.8806 mL
20 mM0.1588 mL0.7940 mL1.5881 mL7.9403 mL
50 mM0.0635 mL0.3176 mL0.6352 mL3.1761 mL
100 mM0.0318 mL0.1588 mL0.3176 mL1.5881 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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