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Givinostat (hydrochloride)

CAS No.
199657-29-9
Chemical Name:
Givinostat (hydrochloride)
Synonyms
ITF2357 HCl;Givinostat Hcl;ITF-2357 hydrochloride;Gavinostat hydrochloride;Givinostat (ITF2357) HCl;Givinostat (hydrochloride);Givinostat HCl. gavinostat;Givinostat (ITF2357) hydrochloride;GAVINOSTAT HYDROCHLORIDE;ITF-2357 HYDROCHLORIDE;inhibit,Givinostat hydrochloride,Histone deacetylases,Givinostat,Inhibitor,HDAC
CBNumber:
CB03041408
Molecular Formula:
C24H28ClN3O4
Molecular Weight:
457.96
MDL Number:
MOL File:
199657-29-9.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

Givinostat (hydrochloride) Properties

storage temp. Store at -20°C
solubility DMSO:45.8(Max Conc. mg/mL);100.01(Max Conc. mM)
FDA UNII Z02132R2QQ

Givinostat (hydrochloride) price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Tocris 6249 Givinostathydrochloride ≥98%(HPLC) 199657-29-9 5 $98 2021-12-16 Buy
Tocris 6249 Givinostathydrochloride ≥98%(HPLC) 199657-29-9 25 $381 2021-12-16 Buy
Crysdot CD31002770 Givinostathydrochloride 98+% 199657-29-9 50mg $251 2021-12-16 Buy
Crysdot CD31002770 Givinostathydrochloride 98+% 199657-29-9 100mg $376 2021-12-16 Buy
Product number Packaging Price Buy
6249 5 $98 Buy
6249 25 $381 Buy
CD31002770 50mg $251 Buy
CD31002770 100mg $376 Buy

Givinostat (hydrochloride) Chemical Properties,Uses,Production

Biological Activity

Givinostat (ITF-2357) hydrochloride is an HDAC inhibitor, inhibits HDAC1 and HDAC3 with IC50 of 198 nM and 157 nM, respectively.

in vitro

Givinostat (hydrochloride) 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.

in vivo

Givinostat (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.

target

hHDAC3

157 nM (IC 50 )

hHDAC1

198 nM (IC 50 )

hHDAC11

292 nM (IC 50 )

hHDAC6

315 nM ( IC 50 )

hHDAC2

325 nM (IC 50 )

hHDAC10

340 nM (IC < sub> 50 )

hHDAC7

524 nM (IC 50 )

hHDAC5

532 nM (IC 50 )

hHDAC9

541 nM (IC 50 )

hHDAC8

854 nM (IC 50 < /sub> )

hHDAC4

1059 nM (IC 50 )

HD1-B

7.5 nM (IC 50 )

HD1-A

16 nM (IC 50 )

HD2

10 nM (IC 50 )

storage

Store at -20°C

Givinostat (hydrochloride) Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 29)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32686 60
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49739 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
Suzhou ARTK Medchem Co., Ltd.
+86-512-68323967 +86-18015559028 sales1@artkmedchem.com China 39009 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
MedChemexpress LLC 021-58955995 sales@medchemexpress.cn United States 4863 58
ShangHai Caerulum Pharma Discovery Co., Ltd. 18149758185 sales-cpd@caerulumpharma.com China 3423 58
Lanzhou Angeli Biochemical Technology Co., Ltd. 0931-8235634 13321316780 1455540579@qq.com China 959 55
Givinostat (hydrochloride) Givinostat Hcl [6-[(Diethylamino)methyl]-2-naphthalenyl]methyl-N-[4-[(hydroxyamino)carbonyl]phenyl]carbamate hydrochloride Givinostat (ITF2357) HCl Gavinostat hydrochloride GAVINOSTAT HYDROCHLORIDE;ITF-2357 HYDROCHLORIDE ITF-2357 hydrochloride Givinostat (ITF2357) hydrochloride Givinostat HCl. gavinostat ITF2357 HCl inhibit,Givinostat hydrochloride,Histone deacetylases,Givinostat,Inhibitor,HDAC 199657-29-9