FKBP12 PROTAC dTAG-13 (dTAG-13) is a FKBP12F36V PROTAC degrader and a PXR partial agonist. FKBP12 PROTAC dTAG-13 induces ubiquitination and proteasomal degradation of proteins tagged with FKBP12F36V, without degrading wild-type FKBP12 or un-fused PXR. It weakly promotes the recruitment of SRC-1, strongly inhibits the interaction between NCoR and PXR, and upregulates the expression of CYP3A4 and other drug metabolism-related genes. FKBP12 PROTAC dTAG-13 is applicable to research related to breast cancer and leukemia[1][2][3].
Molekulargewicht:
1049.17
Reinheit:
99.89
CAS Nummer:
[2064175-41-1]
Formel:
C57H68N4O15
Target-Kategorie:
FKBP,Pregnane X Receptor (PXR),PROTACs
Anwendungsbeschreibung:
MCE Product type: Reference compound
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