JZL195

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

JZL195
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Size Price Stock
250mg$650Check With Us
500mg$980Check With Us
1g$1470Check With Us

Cat #: V2822 CAS #: 1210004-12-8 Purity ≥ 98%

Description: JZL195 is a potent, selective and efficacious dual FAAH/MAGL (fatty acid amide hydrolase/monoacylglycerol lipase) inhibitor with IC50 of 13 nM and 19 nM for mouse brain FAAH and MAGL respectively.

References: Long JZ, et al. Dual blockade of FAAH and MAGL identifies behavioral processes regulated by endocannabinoid crosstalk in vivo. Proc Natl Acad Sci U S A. 2009 Dec 1;106(48):20270-5.

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Product Promise

Promise
Molecular Weight (MW)433.46
Molecular FormulaC₂₄H₂₃N₃O₅
CAS No.1210004-12-8
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: ≥ 42 mg/mLr
Water: < 1mg/mLr
Ethanol: < 1mg/mL
SMILES CodeO=C(N1CCN(CC2=CC=CC(OC3=CC=CC=C3)=C2)CC1)OC4=CC=C([N+]([O-])=O)C=C4
SynonymsJZL195; JZL-195; JZL 195
ProtocolIn VitroJZL195 inhibits rat and human FAAH and MAGL enzymes with IC50 values in the range of ≈10-100 nM based on competitive ABPP assays. JZL195 produces near-complete blockade of FP-Rh labeling of both mouse brain FAAH and MAGL at concentrations as low as 100 nM (IC50 values of 13 and 19 nM, respectively).
In VivoJZL195 (20 mg/kg; i.p.) produces an antinociceptive response in the tail immersion assay.
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
1mM2.3070 mL11.5351 mL23.0702 mL46.1404 mL
5mM0.4614 mL2.3070 mL4.6140 mL9.2281 mL
10mM0.2307 mL1.1535 mL2.3070 mL4.6140 mL
20mM0.1154 mL0.5768 mL1.1535 mL2.3070 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.