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Doxepin hydrochloride

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Catalog No. T1540Cas No. 1229-29-4
Alias Toruan, Novoxapin, Doxepin HCl, Aponal

Doxepin hydrochloride (Aponal) is a dibenzoxepin tricyclic compound. It displays a range of pharmacological actions including maintaining adrenergic innervation. Its mechanism of action is not fully understood, but it appears to block reuptake of monoaminergic neurotransmitters into presynaptic terminals. It also possesses anticholinergic activity and modulates antagonism of histamine H(1)- and H(2)-receptors.

Doxepin hydrochloride

Doxepin hydrochloride

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Purity: 99.91%
Catalog No. T1540Alias Toruan, Novoxapin, Doxepin HCl, AponalCas No. 1229-29-4
Doxepin hydrochloride (Aponal) is a dibenzoxepin tricyclic compound. It displays a range of pharmacological actions including maintaining adrenergic innervation. Its mechanism of action is not fully understood, but it appears to block reuptake of monoaminergic neurotransmitters into presynaptic terminals. It also possesses anticholinergic activity and modulates antagonism of histamine H(1)- and H(2)-receptors.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 g$40InquiryInquiry
2 g$55InquiryInquiry
5 g$89InquiryInquiry
1 mL x 10 mM (in DMSO)$30In 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:99.91%
Appearance:Solid
Color:White to Yellow
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Product Introduction

Doxepin hydrochloride AI Summary
Doxepin hydrochloride shows antiplasmodial activity against various strains of Plasmodium falciparum with IC50 values ranging from 1258.93 nM to 7943.28 nM as determined by the SYBR green assay after 72 hours of incubation. Additionally, it exhibits a wide range of bioactivities against several biological targets, including ROR gamma transcriptional activity, Schistosoma Mansoni Peroxiredoxins, cell-membrane permeable IMPase inhibitors, chronic active B-cell receptor signaling, histone lysine methyltransferase G9a, human tyrosyl-DNA phosphodiesterase 1 (TDP1) both with and without CPT, and Marburg Virus cell binding or entry. Moreover, Doxepin hydrochloride inhibits sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 µM, achieving an inhibition rate of 101.82%..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Doxepin hydrochloride (Aponal) is a dibenzoxepin tricyclic compound. It displays a range of pharmacological actions including maintaining adrenergic innervation. Its mechanism of action is not fully understood, but it appears to block reuptake of monoaminergic neurotransmitters into presynaptic terminals. It also possesses anticholinergic activity and modulates antagonism of histamine H(1)- and H(2)-receptors.
SynonymsToruan, Novoxapin, Doxepin HCl, Aponal
Chemical Properties
Molecular Weight315.84
FormulaC19H22ClNO
Cas No.1229-29-4
SmilesCl.CN(C)CCC=C1c2ccccc2COc2ccccc12
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 60 mg/mL (189.97 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.33 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 mM3.1662 mL15.8308 mL31.6616 mL158.3080 mL
5 mM0.6332 mL3.1662 mL6.3323 mL31.6616 mL
10 mM0.3166 mL1.5831 mL3.1662 mL15.8308 mL
20 mM0.1583 mL0.7915 mL1.5831 mL7.9154 mL
50 mM0.0633 mL0.3166 mL0.6332 mL3.1662 mL
100 mM0.0317 mL0.1583 mL0.3166 mL1.5831 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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%
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