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Lobeline hydrochloride

Name: Lobeline hydrochloride
Brand: TargetMol
SKU: T0268
Price: 30 USD
Availability: InStock
Rating: 5 (10 reviews)

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Catalog No. T0268Cas No. 134-63-4

Alias α-Lobeline hydrochloride, L-Lobeline hydrochloride

Lobeline hydrochloride (α-Lobeline hydrochloride) is a nicotinic receptor agonist, acting as an effective antagonist at both α4β2 and α3β2 neuronal nicotinic receptor subtypes.

Lobeline hydrochloride

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Purity: 99.43%

Catalog No. T0268Alias α-Lobeline hydrochloride, L-Lobeline hydrochlorideCas No. 134-63-4

Lobeline hydrochloride (α-Lobeline hydrochloride) is a nicotinic receptor agonist, acting as an effective antagonist at both α4β2 and α3β2 neuronal nicotinic receptor subtypes.

Pack Size	Price	USA Warehouse	Global Warehouse
25 mg	$30	In Stock	In Stock
50 mg	$44	In Stock	-
100 mg	$80	In Stock	-

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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]

All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.

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Purity:99.43%

Appearance:Solid

Color:White

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COA HPLC HNMR

Product Introduction

Lobeline hydrochloride AI Summary

Lobeline hydrochloride exhibits a broad spectrum of bioactivities against various biological targets. It shows antiplasmodial activity against multiple strains of Plasmodium falciparum, with IC50 values ranging from 3981.07 nM to 15848.93 nM after 72 hours, as measured by the SYBR green assay. The compound is active in several assays, acting as an inhibitor of mitochondrial division, activator of mitochondrial fusion, and inhibitor of Schistosoma Mansoni Peroxiredoxins. It also demonstrates efficacy against Hepatitis C Virus (HCV) and Marburg Virus, and exhibits delayed death inhibition of the malarial parasite plastid. In addition, Lobeline hydrochloride inhibits a wide range of enzymatic and protein interactions, including endonuclease IV, MPP8 Chromodomain, Histone Lysine Methyltransferase G9a, HP1-beta Chromodomain, Polymerase Iota, Human hERG Channel activity, and USP1/UAF1, with potencies ranging from 22.4 nM to 89125.1 nM. The compound shows inhibition of electric eel AChE at 2 mg/ml with a rate of -0.17% and of horse BChE at 2 mg/ml with a 30.37% rate. Additionally, Lobeline hydrochloride significantly inhibits sodium fluorescein uptake in OATP1B3- and OATP1B1-transfected CHO cells at a concentration of 10 µM, with inhibition percentages of 108.46% and 125.57%, respectively. Its antiviral activity is noted against SARS-CoV-2, reducing virus-induced cytotoxicity in Caco-2 and VERO-6 cells at a concentration of 10 µM with varying inhibition rates. Specifically, it showed 24.02% inhibition in Caco-2 cells after 48 hours and -0.02% in VERO-6 cells. Additionally, it inhibits SARS-CoV-2 3CL-Pro protease with an inhibition percentage of 0.3163% at 20 µM. Lobeline hydrochloride also demonstrates moderate antifungal activity against Candida albicans and various antibacterial activities with notable inhibition rates against Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Staphylococcus aureus MRSA. Its impact on cell viability varies across different cell lines, showing both cytotoxic and stimulatory properties in HEK293T, U2OS, and human fibroblast cells. Overall, Lobeline hydrochloride proves to be a versatile compound with diverse biological activities ranging from antiplasmodial and antiviral efficacy to inhibition of various enzymatic processes and cellular growth effects..

Note: Summary generated by AI. Data source: ChEMBL

Bioactivity

Description	Lobeline hydrochloride (α-Lobeline hydrochloride) is a nicotinic receptor agonist, acting as an effective antagonist at both α4β2 and α3β2 neuronal nicotinic receptor subtypes.
Synonyms	α-Lobeline hydrochloride, L-Lobeline hydrochloride

Chemical Properties

Molecular Weight	373.92
Formula	C₂₂H₂₇NO₂·HCl
Cas No.	134-63-4
Smiles	Cl.CN1[C@H](C[C@H](O)c2ccccc2)CCC[C@@H]1CC(=O)c1ccccc1
Relative Density.	no data available

Storage & Solubility Information

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

Solubility Information

DMSO: 45 mg/mL (120.35 mM), Sonication is recommended.

Solution Preparation Table

DMSO

	1mg	5mg	10mg	50mg
1 mM	2.6744 mL	13.3718 mL	26.7437 mL	133.7184 mL
5 mM	0.5349 mL	2.6744 mL	5.3487 mL	26.7437 mL
10 mM	0.2674 mL	1.3372 mL	2.6744 mL	13.3718 mL
20 mM	0.1337 mL	0.6686 mL	1.3372 mL	6.6859 mL
50 mM	0.0535 mL	0.2674 mL	0.5349 mL	2.6744 mL
100 mM	0.0267 mL	0.1337 mL	0.2674 mL	1.3372 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:

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 DMSO TargetMol | 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 DMSO TargetMol | reagent stock solution to 400 μL PEG300 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 ddH₂O TargetMol | 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.

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc