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Olopatadine hydrochloride

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Catalog No. T1170Cas No. 140462-76-6
Alias Olopatadine HCl, KW4679, ALO4943A

Olopatadine hydrochloride (ALO4943A) is an antihistamine with mast-cell stabilizing properties used as eye drops in the treatment of ALLERGIC CONJUNCTIVITIS.

Olopatadine hydrochloride

Olopatadine hydrochloride

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🥰Excellent
Purity: 99.64%
Catalog No. T1170Alias Olopatadine HCl, KW4679, ALO4943ACas No. 140462-76-6
Olopatadine hydrochloride (ALO4943A) is an antihistamine with mast-cell stabilizing properties used as eye drops in the treatment of ALLERGIC CONJUNCTIVITIS.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$35In StockIn Stock
25 mg$61In StockIn Stock
50 mg$87In StockIn Stock
100 mg$123In StockIn Stock
500 mg$277In StockIn Stock
1 mL x 10 mM (in DMSO)$29In 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:99.64%
Appearance:Solid
Color:White
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Product Introduction

Olopatadine hydrochloride AI Summary
Olopatadine hydrochloride exhibits diverse bioactivities across several biological systems. It shows inhibitory effects on passive cutaneous anaphylaxis in rats and IgG1-mediated bronchoconstriction in guinea pigs. Additionally, it has a binding affinity for the histamine H1 receptor and moderate inhibition of the Muscarinic acetylcholine receptor M1. In oncology, it induces DNA re-replication in SW480 colon adenocarcinoma cells at a potency of 1778.3 nM. For antiviral activity, it can block the entry of the Ebola virus with an AC50 of 44.67 µM, inhibit cell viability in Vero E6 cells infected with SARS-CoV-2, and demonstrated inhibition of cytotoxicity in Caco-2 cells exposed to SARS-CoV-2 at a 10 µM concentration with an inhibition of -1.88%. Furthermore, it minimally inhibits the SARS-CoV-2 3CL-Pro protease with -2.774% inhibition at 20 µM. Olopatadine hydrochloride also shows notable antifungal activity against Candida albicans and Cryptococcus neoformans, with inhibition rates of 4.03% and 4.6%, respectively. Its antibacterial effects include activity against Escherichia coli, Klebsiella pneumoniae, and Acinetobacter baumannii, although it shows no inhibition against Pseudomonas aeruginosa and Staphylococcus aureus MRSA..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Olopatadine hydrochloride (ALO4943A) is an antihistamine with mast-cell stabilizing properties used as eye drops in the treatment of ALLERGIC CONJUNCTIVITIS.
SynonymsOlopatadine HCl, KW4679, ALO4943A
Chemical Properties
Molecular Weight373.87
FormulaC21H23NO3·HCl
Cas No.140462-76-6
Smilesc12/C(=C\CCN(C)C)/c3c(COc1ccc(c2)CC(=O)O)cccc3.Cl
Relative Density.1.221 g/cm3
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: 55 mg/mL (147.11 mM), Sonication is recommended.
H2O: 28 mg/mL (74.89 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.35 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
H2O/DMSO
1mg5mg10mg50mg
1 mM2.6747 mL13.3736 mL26.7473 mL133.7363 mL
5 mM0.5349 mL2.6747 mL5.3495 mL26.7473 mL
10 mM0.2675 mL1.3374 mL2.6747 mL13.3736 mL
20 mM0.1337 mL0.6687 mL1.3374 mL6.6868 mL
50 mM0.0535 mL0.2675 mL0.5349 mL2.6747 mL
DMSO
1mg5mg10mg50mg
100 mM0.0267 mL0.1337 mL0.2675 mL1.3374 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:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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

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