Dizocilpine (MK-801)

This product is for research use only, not for human use. We do not sell to patients.

Dizocilpine (MK-801)
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Size Price Stock
250mg$650Check With Us
500mg$980Check With Us
1g$1470Check With Us

Cat #: V5684 CAS #: 77086-21-6 Purity ≥ 98%

Description: Dizocilpine (MK-801), is a novel, potent, selective and non-competitive NMDA ( N-Methyl-D-aspartate) receptor antagonist with Kd of 37.2 nM in rat brain membranes.

References: Dizocilpine (MK 801) (1 mg/kg) treatment before each METH injection reduces the extent of DA depletion by 55% in striatal of mice. Dizocilpine (MK 801) (1 mg/kg) also attenuates the effects of METH on microglial activation in striatal of mice

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Molecular Weight (MW)221.303
Molecular FormulaC16H15N
CAS No.77086-21-6
SMILES CodeC[C@]1(N2)C3=CC=CC=C3CC2C4=CC=CC=C14
SynonymsDizocilpine; MK801; MK 801; MK-801; MK 801 Maleate; Related CAS#: 77086-21-6 (free base);
ProtocolIn VitroDizocilpine (MK-801; <500 μM) inhibits activation of microglia induced by LPS with increased Cox-2 protein expression in BV-2 cells. Dizocilpine (<500 μM) reduces microglial TNF-α output with an EC50 of 400 μM in BV-2 cells
In VivoDizocilpine (MK 801) (1 mg/kg) treatment before each METH injection reduces the extent of DA depletion by 55% in striatal of mice. Dizocilpine (MK 801) (1 mg/kg) also attenuates the effects of METH on microglial activation in striatal of mice
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM4.5187 mL22.5935 mL45.1869 mL90.3738 mL
5mM0.9037 mL4.5187 mL9.0374 mL18.0748 mL
10mM0.4519 mL2.2593 mL4.5187 mL9.0374 mL
20mM0.2259 mL1.1297 mL2.2593 mL4.5187 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

Calculation Results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in µL DMSO(Master liquid concentration mg/mL) ,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation: Take µL DMSO master liquid, next add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.