ST7612AA1 is a histone deacetylase (HDAC) inhibitor that controls chromatin condensation and DNA transcription by removing acetyl groups from histones. ST7612AA1 is also a potent HIV reactivation inducer, and its reactivation activity is exerted without activating or proliferating CD4+T cells, and can be used in the study of HIV reactivation strategies and elimination of viral reservoirs[1].
Molekulargewicht:
405.51
CAS Nummer:
[1428535-92-5]
Formel:
C20H27N3O4S
Target-Kategorie:
DNA/RNA Synthesis,HDAC,HIV
Anwendungsbeschreibung:
MCE Product type: Reference compound
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