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Dipivefrin hydrochloride

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Catalog No. T0103Cas No. 64019-93-8
Alias Dipivefrin HCL

Dipivefrin hydrochloride (Dipivefrin HCl) that is available as an ophthalmic solution is a prodrug of adrenaline, which is used to treat glaucoma.

Dipivefrin hydrochloride

Dipivefrin hydrochloride

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Purity: 99.96%
Catalog No. T0103Alias Dipivefrin HCLCas No. 64019-93-8
Dipivefrin hydrochloride (Dipivefrin HCl) that is available as an ophthalmic solution is a prodrug of adrenaline, which is used to treat glaucoma.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$48In StockIn Stock
50 mg$77In StockIn Stock
100 mg$118In StockIn Stock
200 mg$178In 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]
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:99.96%
Color:White
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Product Introduction

Dipivefrin hydrochloride AI Summary
Dipivefrin hydrochloride exhibits bioactivity across a diverse range of biological assays with varying potencies: 1. Inhibits AmpC Beta-Lactamase with a potency of 2818.4 nM. 2. Acts as a beta-arrestin-biased ligand for the beta2-adrenergic receptor with potencies of 1458.1 nM and 259.3 nM in different assays. 3. Possesses delayed death inhibitory activity against the malarial parasite plastid with potencies of 18526.0 nM (96-hour incubation) and 11689.1 nM (48-hour incubation). 4. Inhibits Polymerase Iota with a potency of 89125.1 nM. 5. Shows inhibitory activity against TGF-b in a cytotoxic counterscreen assay with a potency of 12589.3 nM. 6. Functions as a Beta-2AR agonist with an EC50 of 7130.0 nM via the FAP method. 7. Inhibits Hepatitis C Virus (HCV) with a potency of 501.2 nM. 8. Acts as an inverse agonist for the GLP-1 receptor with a potency of 3981.1 nM. 9. Inhibits human tyrosyl-DNA phosphodiesterase 1 (TDP1) with identical potencies of 9034.9 nM both in the presence and absence of CPT. 10. Inhibits PTHR with a potency of 1995.3 nM. 11. Validated as a GLP-1 receptor agonist with potencies of 69.9 nM and 82.0 nM in different validation assays. Additionally, Dipivefrin hydrochloride exhibits slight inhibition of cell viability in Vero E6 cells infected with SARS-CoV-2, with an inhibition index of 1.01 in comparison to the arbidol control, suggesting some potential antiviral activity although the overall effect is relatively modest. These results collectively indicate that Dipivefrin hydrochloride has potential multifaceted pharmacological properties..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Dipivefrin hydrochloride (Dipivefrin HCl) that is available as an ophthalmic solution is a prodrug of adrenaline, which is used to treat glaucoma.
SynonymsDipivefrin HCL
Chemical Properties
Molecular Weight387.9
FormulaC19H27NO5·HCl
Cas No.64019-93-8
SmilesCl.CNCC(O)c1ccc(OC(=O)C(C)(C)C)c(OC(=O)C(C)(C)C)c1
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: 50 mg/mL (128.9 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.16 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 mM2.5780 mL12.8899 mL25.7798 mL128.8992 mL
5 mM0.5156 mL2.5780 mL5.1560 mL25.7798 mL
10 mM0.2578 mL1.2890 mL2.5780 mL12.8899 mL
20 mM0.1289 mL0.6445 mL1.2890 mL6.4450 mL
50 mM0.0516 mL0.2578 mL0.5156 mL2.5780 mL
100 mM0.0258 mL0.1289 mL0.2578 mL1.2890 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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