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Givinostat (ITF2357)
Cat. No.:
OB0225WX-2470
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
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Product Overview
Description:
Givinostat (ITF2357) is a potent pan-HDAC inhibitor with IC50 values of 10 nM, 7.5 nM, and 16 nM for maize HD2, HD1B, and HD1A, respectively.
Synonym:
732302-99-7; Givinostat hydrochloride monohydrate; Givinostat Hydrochloride Hydrate; Givinostat (ITF2357); ITF2357; ITF2357 (Givinostat); (6-((diethylamino)methyl)naphthalen-2-yl)methyl (4-(hydroxycarbamoyl)phenyl)carbamate hydrochloride hydrate; [6-(diethylaminomethyl)naphthalen-2-yl]methyl N-[4-(hydroxycarbamoyl)phenyl]carbamate;hydrate;hydrochloride; ITF-2357 hydrochloride monohydrate; Givinostat (hydrochloride monohydrate); {6-[(diethylamino)methyl]naphthalen-2-yl}methyl N-[4-(hydroxycarbamoyl)phenyl]carbamate hydrate hydrochloride; Givinostat hydrochloride (USAN); {6-[(diethylamino)methyl]naphthalen-2-yl}methyl [4-(hydroxycarbamoyl)phenyl]carbamate hydrochloride hydrate; Carbamic acid, (4-((hydroxyamino)carbonyl)phenyl)-, (6-((diethylamino)methyl)-2-naphthalenyl)methyl ester, monohydrochloride, monohydrate
CAS No.:
732302-99-7
Compound CID:
9804991
Formula:
C24H27N3O4·HCl·H2O
Formula Weight:
475.97
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Givinostat (ITF2357) is applied in epigenetic and hematology research as a potent histone deacetylase (HDAC) inhibitor to study the modulation of pro-inflammatory cytokines and the regulation of hematopoietic cell proliferation.
Library Information
Target:
HDAC
Receptor:
HD2; HD1B; HD1A
Pathways:
Cytoskeletal signaling
Plate Number:
L6700-03
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
95 mg/mL; 199.59 mM
ALogP:
4.046
HBA_Count:
3
HBD_Count:
2
Rotatable Bond:
9





