基本信息
文件名称:HDAC3-IN-6-生命科学试剂-MCE.pdf
文件大小:460.25 KB
总页数:1 页
更新时间:2025-03-11
总字数:约2.25千字
文档摘要

Hotline:400-820-3792

Inhibitors?ScreeningLibraries?Proteins

www.MedChemE

HDAC3-IN-6

Cat.No.:HY-172133

分?式:C??H??N?O?

分?量:417.46

作?靶点:HDAC;PD-1/PD-L1;Apoptosis;ReactiveOxygenSpecies

作?通路:CellCycle/DNADamage;Epigenetics;

Immunology/Inflammation;Apoptosis;Metabolic

Enzyme/Protease;NF-κB

储存?式:Pleasestoretheproductundertherecommendedconditionsin

theCertificateofAnalysis.

BIOLOGICALACTIVITY

?物活性HDAC3-IN-6(CompoundSC26)是?种选择性HDAC3抑制剂,IC50为53nM。HDAC3-IN-6剂量依赖性地诱

导PD-L1的表达。HDAC3-IN-6诱导更明显的凋亡(Apoptosis)和ROS的产?。HDAC3-IN-6对结直肠癌表现

出?的抗肿瘤功效[1]。

IC50TargetHDAC1HDAC3

3.98μM(IC50)53nM(IC50)

REFERENCES

[1].SunZ,etal.DiscoveryofNovelHydrazide-BasedHDAC3InhibitorsasEpigeneticImmunomodulatorsforCancerImmunotherapy.J

MedChem.2025Feb13;68(3):3048-3064.

McePdfHeight

Caution:Producthasnotbeenfullyvalidatedformedicalapplications.

Forresearchuseonly.