JNJ-7777120

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

JNJ-7777120
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Size Price Stock
250mg$750Check With Us
500mg$1150Check With Us
1g$1725Check With Us

Cat #: V1239 CAS #: 459168-41-3 Purity ≥ 98%

Description: JNJ-7777120 (JNJ7777120; JNJ 7777120), an indole analog, is a potent and selective non-imidazole-based histamine H4R receptor antagonist that can reduce allergic and asthmatic symptoms.

References: Thurmond RL, et al. A potent and selective histamine H4 receptor antagonist with anti-inflammatory properties. J Pharmacol Exp Ther. 2004 Apr;309(1):404-13. 

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Product Promise

Promise
Molecular Weight (MW)277.75
Molecular FormulaC14H16ClN3O
CAS No.459168-41-3
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 56 mg/mL (201.6 mM)r
Water: <1 mg/mLr
Ethanol: 8 mg/mL (28.8 mM)
Solubility In Vivo30% Propylene glycol, 5% Tween 80, 65% D5W: 20 mg/mL
SynonymsJNJ7777120; JNJ-7777120; JNJ 7777120
ProtocolIn VitroJNJ-7777120 (0, 10, 100, 1000 nM; ~6 h) shows functional antagonism of the human and mouse histamine H4 receptors in SK-N-MC cells
In VivoJNJ-7777120 shows equipotent against the human, mouse, and rat receptors and exhibits at least 1000-fold selectivity over H1, H2, or H3 receptors
Animal modelBALB/c mice
Formulation20 mg/kg
AdministrationSubcutaneous injection; single daily for 2 days
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
1mM3.6004 mL18.0018 mL36.0036 mL72.0072 mL
5mM0.7201 mL3.6004 mL7.2007 mL14.4014 mL
10mM0.3600 mL1.8002 mL3.6004 mL7.2007 mL
20mM0.1800 mL0.9001 mL1.8002 mL3.6004 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.