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Droperidol

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Catalog No. T0990Cas No. 548-73-2
Alias NSC 169874, Dehydrobenzperidol

Droperidol (Dehydrobenzperidol) is a Dopamine-2 Receptor Antagonist. The mechanism of action of droperidol is as a Dopamine D2 Antagonist.

Droperidol

Droperidol

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Purity: 98%
Catalog No. T0990Alias NSC 169874, DehydrobenzperidolCas No. 548-73-2
Droperidol (Dehydrobenzperidol) is a Dopamine-2 Receptor Antagonist. The mechanism of action of droperidol is as a Dopamine D2 Antagonist.
Pack SizePriceAvailabilityQuantity
100 mg$39In Stock
200 mg$55In Stock
500 mg$91In Stock
1 mL x 10 mM (in DMSO)$43In Stock
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Purity:98%
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Product Introduction

Bioactivity
Description
Droperidol (Dehydrobenzperidol) is a Dopamine-2 Receptor Antagonist. The mechanism of action of droperidol is as a Dopamine D2 Antagonist.
In vitro
Droperidol has a dual effect on repolarization, prolonging the development of EADs and the subsequent triggering of activity in rabbit Purkinje fibers at low concentrations. In rabbit Purkinje fibers stimulated with 60 pulses/min, 0.01 mM-0.3 mM Droperidol increased action potential duration (APD) in a dose-dependent manner without altering other parameters.1 mM-3 mM Droperidol resulted in a reversal of the prolongation effect in rabbit Purkinje fibers.10 mM- 30 mM Droperidol produced a shortening of the APD at 50% repolarization, accompanied by significant reductions in Vmax, action potential amplitude, and resting membrane potential in rabbit Purkinje fibers. A single dose of 3 mg/kg Droperidol not only dose-dependently reduced activity and rearing frequency in the open-field experiment, but also reduced the Apomorphine effect in rats.Droperidol (3 mg/kg, long-term administration) induced significant tolerance to all activity parameters recorded in the rat open field.
In vivo
Droperidol has been shown to block potassium efflux from the myocardium of isolated animal ventricular myocytes, resulting in a dose-dependent delay in repolarization.Droperidol also induces early depolarization of Purkinje fibers in isolated animals.Droperidol produces mild alpha-adrenergic blockade and peripheral vasodilation.
AliasNSC 169874, Dehydrobenzperidol
Chemical Properties
Molecular Weight379.43
FormulaC22H22FN3O2
Cas No.548-73-2
SmilesO=C1N(C=2C(N1)=CC=CC2)C=3CCN(CCCC(=O)C4=CC=C(F)C=C4)CC3
Relative Density.1.269g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 65 mg/mL (171.31 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6355 mL13.1777 mL26.3553 mL131.7766 mL
5 mM0.5271 mL2.6355 mL5.2711 mL26.3553 mL
10 mM0.2636 mL1.3178 mL2.6355 mL13.1777 mL
20 mM0.1318 mL0.6589 mL1.3178 mL6.5888 mL
50 mM0.0527 mL0.2636 mL0.5271 mL2.6355 mL
100 mM0.0264 mL0.1318 mL0.2636 mL1.3178 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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