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Harmine hydrochloride

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Catalog No. T2811Cas No. 343-27-1
Alias telepathine hydrochloride

Harmine hydrochloride (telepathine hydrochloride) is extracted from Peganum Harmala Genus.

Harmine hydrochloride

Harmine hydrochloride

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Purity: 99.84%
Catalog No. T2811Alias telepathine hydrochlorideCas No. 343-27-1
Harmine hydrochloride (telepathine hydrochloride) is extracted from Peganum Harmala Genus.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 mg$41In StockIn Stock
100 mg$66In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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Purity:99.84%
Color:White to Yellow
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Product Introduction

Harmine hydrochloride AI Summary
Harmine hydrochloride exhibits a broad spectrum of bioactivities, implicating its potential for diverse pharmacological applications. It functions as a potent inhibitor of lipid storage modulators, Nrf2, Histone Lysine Methyltransferase G9a, BAZ2B, Human Flap endonuclease 1 (FEN1), and several enzymes linked to DNA repair and cellular signaling such as RAD54, ELG1-dependent DNA repair, and tyrosyl-DNA phosphodiesterase 1 (TDP1). It also displays moderate potency in targeting chronic active B-cell receptor signaling and Schistosoma Mansoni Peroxiredoxins. The compound shows modulatory effects on RanGTP induced Rango and the activity of kallikrein-7 (K7) zymogen. Additionally, Harmine hydrochloride demonstrates significant inhibitory activity against electric eel acetylcholinesterase (AChE) and horse butyrylcholinesterase (BChE), with inhibition rates of 50.86% and 12.05% respectively at a concentration of 2 mg/ml, indicating potential as a cholinesterase inhibitor. It also exhibits cytotoxicity against human HL cells with an 87.3% activity at 50 µM after 72 hours and showcases antichlamydial activity against Chlamydia pneumoniae K7 infected in HL cells with a 26.0% inhibition rate at 50 µM after 70 hours. Furthermore, the compound induces genotoxicity in human embryonic kidney cells and DNA re-replication in MCF 10a normal breast cells and SW480 colon adenocarcinoma cells. It inhibits cell surface uPA generation, CF-induced NF-kB activation, and delays death in the malaria parasite plastid. Additionally, Harmine hydrochloride has notable antiviral activity by inhibiting Hepatitis C Virus (HCV) and activates ClpP. Overall, Harmine hydrochloride's wide range of bioactivities underscores its potential for extensive therapeutic implications and warrants further investigation..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Harmine hydrochloride (telepathine hydrochloride) is extracted from Peganum Harmala Genus.
Targets&IC50
MNB:149 nM, DYRK1A:33 nM, 5-HT2A receptor:397 nM (Ki), DYRK2:1.9 μM, DYRK1B:166 nM
Synonymstelepathine hydrochloride
Chemical Properties
Molecular Weight248.71
FormulaC13H13ClN2O
Cas No.343-27-1
SmilesCl.COc1ccc2c(c1)[nH]c1c(C)nccc21
Relative Density.no data available
Storage & Solubility Information
Storagekeep away from moisture,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 2 mg/mL (8.04 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.0207 mL20.1037 mL40.2075 mL201.0374 mL
5 mM0.8041 mL4.0207 mL8.0415 mL40.2075 mL

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In Vivo Formulation Calculator (Clear solution)

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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