HDAC1-IN-5 is a potent HDAC1 inhibitor with IC50 values of 15 nM and 20 nM for HDAC1 and HDAC6, respectively. HDAC1-IN-5 can enhance the acetylation of histone H3 and alpha-tubulin, as well as promote the activation of caspase 3 in cancer cells, thereby inducing apoptosis. HDAC1-IN-5 induces chromatin damage by binding with DNA. HDAC1-IN-5 has strong inhibitory activity against tumor growth in xenograft mice[1].
Molekulargewicht:
367.46
Formel:
C20H21N3O2S
Target-Kategorie:
Apoptosis,Caspase,HDAC,Microtubule/Tubulin
Anwendungsbeschreibung:
MCE Product type: Reference compound
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