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Metoclopramide hydrochloride

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Catalog No. T1069Cas No. 7232-21-5
Alias Metoclopramide HCl, Maxolon

Metoclopramide hydrochloride (Metoclopramide HCl) is a selective dopamine D2 receptor antagonist, used as an antiemetic.

Metoclopramide hydrochloride

Metoclopramide hydrochloride

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🥰Excellent
Purity: 99.99%
Catalog No. T1069Alias Metoclopramide HCl, MaxolonCas No. 7232-21-5
Metoclopramide hydrochloride (Metoclopramide HCl) is a selective dopamine D2 receptor antagonist, used as an antiemetic.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$33In StockIn Stock
25 mg$50In StockIn Stock
50 mg$71In StockIn Stock
100 mg$92In StockIn Stock
200 mg$147In StockIn Stock
500 mg$243In StockIn Stock
1 mL x 10 mM (in DMSO)$39In StockIn 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:99.99%
Appearance:Solid
Color:White
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Product Introduction

Metoclopramide hydrochloride AI Summary
Metoclopramide hydrochloride exhibits a broad range of bioactivities across different assays and biological models. It demonstrates antiplasmodial activity against Plasmodium falciparum W2 with a pIC25 value of 4.9, measured using the SYBR green assay over 72 hours. The compound shows specific potency as a Rab9 Promoter Activator at 5623.4 nM and exhibits an IC50 greater than 50000.0 nM as an Estrogen Receptor-beta Coactivator Binding Inhibitor. Additionally, it acts as a differential inhibitor of the proliferation of Plasmodium falciparum line W2 at 15848.9 nM, and inhibits MPP8 Chromodomain interactions with Methylated Histone Tails at a potency of 89125.1 nM, and HP1-beta Chromodomain interactions at 10000.0 nM. Among its notable activities, it inhibits Histone Lysine Methyltransferase G9a at 22.4 nM and the ERG Ets/DNA interaction at 50118.7 nM. In cellular assays, Metoclopramide hydrochloride significantly inhibits sodium fluorescein uptake in OATP1B1 and OATP1B3-transfected CHO cells by 84.82% and 108.21% respectively at 10 µM. In a Wistar rat gastroparesis model, the compound improves gastric emptying by 41.0% at 10 mg/kg when administered intravenously post-meal, as measured after 15 minutes using a colorimetric method. Despite these activities, it shows very low efficacy in inhibiting cell viability in Vero E6 cells infected with SARS-CoV-2 (strain BavPat1), with an inhibition index of 0.02423 at a low MOI of 0.002 after 72 hours. Furthermore, Metoclopramide hydrochloride displays modest antifungal activity against Candida albicans (3.69% inhibition) and antibacterial activity against Klebsiella pneumoniae (10.19%), Pseudomonas aeruginosa (3.44%), Acinetobacter baumannii (16.26%), and Staphylococcus aureus MRSA (7.88%). However, it has negative inhibition rates against Cryptococcus neoformans (-1.39%) and Escherichia coli (-6.93%)..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Metoclopramide hydrochloride (Metoclopramide HCl) is a selective dopamine D2 receptor antagonist, used as an antiemetic.
Targets&IC50
5-HT3 receptor:308 nM (IC50), D2 receptor:483 nM (IC50)
SynonymsMetoclopramide HCl, Maxolon
Chemical Properties
Molecular Weight336.26
FormulaC14H22ClN3O2·HCl
Cas No.7232-21-5
SmilesCl.CCN(CC)CCNC(=O)c1cc(Cl)c(N)cc1OC
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
Ethanol: 62 mg/mL (184.38 mM), Sonication is recommended.
H2O: 61 mg/mL (181.41 mM), Sonication is recommended.
DMSO: 50 mg/mL (148.69 mM), Sonication is recommended.
Solution Preparation Table
DMSO/H2O/Ethanol
1mg5mg10mg50mg
1 mM2.9739 mL14.8694 mL29.7389 mL148.6945 mL
5 mM0.5948 mL2.9739 mL5.9478 mL29.7389 mL
10 mM0.2974 mL1.4869 mL2.9739 mL14.8694 mL
20 mM0.1487 mL0.7435 mL1.4869 mL7.4347 mL
50 mM0.0595 mL0.2974 mL0.5948 mL2.9739 mL
100 mM0.0297 mL0.1487 mL0.2974 mL1.4869 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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%
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Dose Conversion

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