Givinostat HCl

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

Givinostat HCl
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
250mg$1240Check With Us
500mg$1750Check With Us
1g$2625Check With Us

Cat #: V3844 CAS #: 199657-29-9 Purity ≥ 98%

Description: Givinostat (ITF-2357 hydrochloride) is a potent and orally bioactive HDAC inhibitor with potential anti-inflammatory, anti-angiogenic, and anticancer activities.

References: Li S, et al. Specific inhibition of histone deacetylase 8 reduces gene expression and production of proinflammatory cytokines in vitro and in vivo. J Biol Chem. 2015 Jan 23;290(4):2368-78.

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Molecular Weight (MW)457.96
Molecular FormulaC24H27N3O4.HCl
CAS No.199657-29-9
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: >100 mg/mLr
Water: <1 mg/mLr
Ethanol: 3 mg/mL
Solubility In Vivo30% propylene glycol, 5% Tween 80, 65% D5W: 30 mg/mL
SynonymsITF-2357 HCl; ITF 2357; ITF2357; Givinostat HCl ; gavinostat;
ProtocolIn VitroGivinostat (ITF2357) suppresses total LPS-induced IL-1β production robustly compared with the reduction by ITF3056. At 25, 50, and 100 nM, Givinostat reduces IL-1β secretion more than 70%. Givinostat suppresses the production of IL-6 in PBMCs stimulated with TLR agonists as well as the combination of IL-12 plus IL-18. IL-6 secretion decreases to 50% at 50 nM Givinostat, but at 100 and 200 nM, there is no reduction
In VivoGivinostat (ITF2357) at 10 mg/kg is used as a positive control and reduces serum TNFα by 60%. Pretreatment of Givinostat (ITF-2357) starting at 0.1 mg/kg significantly reduces the circulating TNFα by nearly 90%. To achieve a significant increase in serum IL-1β production, a higher dose of LPS is injected (10 mg/kg), and blood is collected after 4 h
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
1mM2.1836 mL10.9180 mL21.8360 mL43.6719 mL
5mM0.4367 mL2.1836 mL4.3672 mL8.7344 mL
10mM0.2184 mL1.0918 mL2.1836 mL4.3672 mL
20mM0.1092 mL0.5459 mL1.0918 mL2.1836 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
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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.