HDAC6-IN-72 is a HDAC6 zinc finger ubiquitin-binding domain (ZnF-UBD) inhibitor that inhibits the interaction between HDAC6 ZnF-UBD and ubiquitin with an IC50 of 2.7 µM. HDAC6-IN-72 can be used for the research of breast cancer, colorectal cancer, multiple myeloma[1].
Molecular Weight:
395.41
Formula:
C21H21N3O5
Target:
HDAC
Application Notes:
MCE Product type: Reference compound
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