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PROTAK™ MZP-55

E31P33363-1DatasheetCOAMSDS
$1310/ 5mg
Specification
Quantity
Total: $1310

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Product Information

CAS No.2010159-48-3
Purity>98.00%
FormulaC57H70ClN7O10S
M.W.1080.72
SolubilitySoluble in DMSO
Storage/StabilityStore at -20°C
BackgroundMZP-55 is a selective degrader of BRD3/4 based on PROTAC technology, with a Kd of 8 nM for Brd4BD2.MZP-55 is a selective degrader of BRD3/4 based on PROTAC technology, with a Kd of 8 nM for Brd4BD2. MZP-55 binds to VHL-EloC-EloB protein (VCB) with a Kd of 105 ± 24 nM. MZP-55 shows an inhibitory activity against MV4;11 and HL60 cells, with pEC50s of 7.31 ± 0.03 and 6.57 ± 0.02, respectivel. Chan KH, et al. Impact of Target Warhead and Linkage Vector on Inducing Protein Degradation: Comparison of Bromodomain and Extra-Terminal (BET) Degraders Derived from Triazolodiazepine (JQ1) and Tetrahydroquinoline (I-BET726) BET Inhibitor Scaffolds. J Med Chem.
Price1310$