UBX-382 is an orally active BTK PROTAC degrader with a DC50 of 4.56 nM. UBX-382 inhibits B-cell receptor signaling by targeting BTK. UBX-382 shows superior degradation activity for wild-type and mutant BTK proteins. UBX-382 inhibits tumor growth in murine xenograft models harboring wild-type or C481S mutant BTK-expressing TMD-8 cells. UBX-382 can be used for the study of B-cell-related blood cancers[1].
Molecular Weight:
752.86
Purity:
96.20
CAS Number:
[2884554-45-2]
Formula:
C42H44N10O4
Target:
Btk,ERK,MEK,PROTACs,Syk
Application Notes:
Reference compound
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