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199657-29-9

中文名称 199657-29-9
英文名称 Givinostat (hydrochloride)
CAS 199657-29-9
分子式 C24H28ClN3O4
分子量 457.95
MOL 文件 199657-29-9.mol
更新日期 2025/10/09 14:24:25
199657-29-9 结构式 199657-29-9 结构式

基本信息

中文别名
化合物 T6279L
化合物GIVINOSTAT HYDROCHLORIDE
英文别名
Givinostat Hcl
ITF-2357 hydrochloride
Gavinostat hydrochloride
Givinostat (ITF2357) HCl
Givinostat (hydrochloride)
Givinostat (ITF2357) hydrochloride
GAVINOSTAT HYDROCHLORIDE
ITF-2357 HYDROCHLORIDE
[6-[(Diethylamino)methyl]-2-naphthalenyl]methyl-N-[4-[(hydroxyamino)carbonyl]phenyl]carbamate hydrochloride
所属类别
生物化工:激动剂抑制剂

物理化学性质

储存条件-20°C储存
溶解度DMSO:45.8(Max Conc. mg/mL);100.01(Max Conc. mM)
形态Solid
颜色White to off-white
199657-29-9价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2025/05/22HY-14842A199657-29-9
Givinostat hydrochloride
199657-29-95 mg900元
2025/05/22HY-14842A199657-29-9
Givinostat hydrochloride
199657-29-910 mM * 1 mLin DMSO907元
2025/05/22HY-14842A199657-29-9
Givinostat hydrochloride
199657-29-910 mg1600元

常见问题列表

生物活性
Givinostat (ITF-2357) hydrochloride 是 HDAC 抑制剂,抑制 HDAC1 和 HDAC3,IC50 分别为 198 nM 和 157 nM。
靶点

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 50 )

hHDAC7

524 nM (IC 50 )

hHDAC5

532 nM (IC 50 )

hHDAC9

541 nM (IC 50 )

hHDAC8

854 nM (IC 50 )

hHDAC4

1059 nM (IC 50 )

HD1-B

7.5 nM (IC 50 )

HD1-A

16 nM (IC 50 )

HD2

10 nM (IC 50 )

体外研究

Givinostat (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. Givinostat (ITF-2357) inhibits JS-1 cell proliferation in a concentration-dependent manner in the CCK-8 assay. Treatment with Givinostat (ITF-2357) ≥500 nM is associated with significant inhibition of JS-1 cell proliferation. Also, the cell inhibition rate significantly differs between the group cotreated with Givinostat (ITF-2357) ≥250 nM plus LPS and the group without LPS treatment.

体内研究

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.

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