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Halopemide

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Catalog No. T15461Cas No. 59831-65-1

Halopemide is a potent inhibitor of PLD (IC50 = 220 and 310 nM for human PLD1 and PLD2). Halopemid is an antagonist of dopamine receptors. Halopemid can be used in psychotropic research.

Halopemide

Halopemide

🥰Excellent
Purity: 96.29%
Catalog No. T15461Cas No. 59831-65-1
Halopemide is a potent inhibitor of PLD (IC50 = 220 and 310 nM for human PLD1 and PLD2). Halopemid is an antagonist of dopamine receptors. Halopemid can be used in psychotropic research.
Pack SizePriceAvailabilityQuantity
1 mg$29In Stock
5 mg$77In Stock
10 mg$128In Stock
25 mg$257In Stock
50 mg$383In Stock
100 mg$557In Stock
1 mL x 10 mM (in DMSO)$86In Stock
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Purity:96.29%
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Product Introduction

Bioactivity
Description
Halopemide is a potent inhibitor of PLD (IC50 = 220 and 310 nM for human PLD1 and PLD2). Halopemid is an antagonist of dopamine receptors. Halopemid can be used in psychotropic research.
Targets&IC50
PLD1:220 nM, PLD2:310 nM
In vitro
In transdifferentiated MOVAS cells, Halopemide (1-2 μM; 21 days) influences calcification[1].
In vivo
In the majority of monkeys tested, Halopemide (10 mg/kg; p.o.) causes dyskinesias[2].
Chemical Properties
Molecular Weight416.88
FormulaC21H22ClFN4O2
Cas No.59831-65-1
SmilesFc1ccc(cc1)C(=O)NCCN1CCC(CC1)n1c2ccc(Cl)cc2[nH]c1=O
Relative Density.1.337g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 55 mg/mL (131.93 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3988 mL11.9939 mL23.9877 mL119.9386 mL
5 mM0.4798 mL2.3988 mL4.7975 mL23.9877 mL
10 mM0.2399 mL1.1994 mL2.3988 mL11.9939 mL
20 mM0.1199 mL0.5997 mL1.1994 mL5.9969 mL
50 mM0.0480 mL0.2399 mL0.4798 mL2.3988 mL
100 mM0.0240 mL0.1199 mL0.2399 mL1.1994 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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