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| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
MZP-55 is a PROTAC connected by ligands for von Hippel-Lindau and BRD3/4 , with a K d of 8 nM for Brd4 BD2 .
In Vitro
MZP-55 is a selective degrader of BRD3/4 based on PROTAC technology, with a K d of 8 nM for Brd4 BD2 . MZP-55 binds to VHL-EloC-EloB protein (VCB) with a K d of 105 ± 24 nM. MZP-55 shows an inhibitory activity against MV4;11 and HL60 cells, with pEC 50 s of 7.31 ± 0.03 and 6.57 ± 0.02, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
IC50& Target:Kd: 8 nM (Brd4 BD2 )
| Isomeric SMILES | C[C@H]1C[C@H](C2=C(N1C(=O)C)C=CC(=C2)C3=CC=C(C=C3)C(=O)NCCOCCOCCOCCOCC(=O)N[C@H](C(=O)N4C[C@@H](C[C@H]4C(=O)NCC5=CC=C(C=C5)C6=C(N=CS6)C)O)C(C)(C)C)NC7=CC=C(C=C7)Cl |
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| Alternate CAS | 2010159-48-3 |
| PubChem CID | 122539896 |
| Molecular Weight | 1080.72 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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