JSH-23

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

JSH-23
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Size Price Stock
250mg$700Check With Us
500mg$950Check With Us
1g$1425Check With Us

Cat #: V0765 CAS #: 749886-87-1 Purity ≥ 98%

Description: JSH-23 (JSH23; JSH 23) was designed as a nove and potent inhibitor of NF-κB transcriptional activity with potential anti-inflammatory and anti-diabetic activity.

References: Shin HM, et al. Inhibitory action of novel aromatic diamine compound on lipopolysaccharide-induced nuclear translocation of NF-kappaB without affecting IkappaB degradation. FEBS Lett. 2004 Jul 30;571(1-3):50-4.

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Molecular Weight (MW)240.34
Molecular FormulaC16H20N2
CAS No.749886-87-1
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 48 mg/mL (199.7 mM)r
Water: <1 mg/mLr
Ethanol: 20 mg/mL (83.2 mM)
SMILES CodeNC1=CC(C)=CC=C1NCCCC2=CC=CC=C2
SynonymsJSH 23; JSH-23; JSH23;
ProtocolIn VitroNuclear amount of NF-κB p65 is markedly increased upon exposure to LPS for 1 h. Treatment of JSH-23 (30 μM; 1 hours) to LPS- stimulated RAW 264.7 cells decreases nuclear content of NF-κB p65 in a dose-dependent manner. JSH-2 (1-300 μM; 24 hours) at <100 μM does not show significant cytotoxic effects on the RAW 264.7 cells.
In VivoJSH-23 (1 mg/kg, 3 mg/kg; orally administered; daily; for 2 weeks) significantly reverses the nerve conduction and nerve blood flow deficits seen in diabetic rats.
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
1mM4.1608 mL20.8039 mL41.6077 mL83.2154 mL
5mM0.8322 mL4.1608 mL8.3215 mL16.6431 mL
10mM0.4161 mL2.0804 mL4.1608 mL8.3215 mL
20mM0.2080 mL1.0402 mL2.0804 mL4.1608 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.