PROTAC PAPD5 degrader 1 (compound 12b) inhibits both hepatitis A (HAV) and hepatitis B virus (HBV) in vitro and in vivo[1], with IC50 and CC50 of 10.59 µM and > 50 µM, respectively in Huh7 cells[1].
Molecular Weight:
978.05
Formula:
C49H63N5O16
Target:
HBV,PROTACs
Application Notes:
MCE Product type: Reference compound
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