dBAZ2B
dBAZ2B is a BAZ2B PROTAC degrader, with a DC50 of 19 nM. (Pink: BAZ2A/B ligand (HY-168449); Black: linker (HY-168450); Blue: VHL Ligand (HY-125905))
(Pink: BAZ2B ligand (HY-168449); Blue: VHL ligand (HY-125905); Black: linker (HY-168450)).
For research use only. We do not sell to patients.
- CAS No.: 3104449-58-0
- Formula: C55H66FN11O6S
- Molecular Weight:1028.25
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All PROTACs Isoforms
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Biological Activity
Description
In Vitro
dBAZ2B (0.25 μM; 2-72 h) selectively degrades BAZ2B in PC3 cells with a DC50 of 19 nM (Dmax ≥ 95%), increases BAZ2A levels with an EC50 of 35 nM, achieves substantial BAZ2B degradation within 2 h that persists for at least 72 h, and acts via a bromodomain-binding, VHL-dependent, proteasome-mediated mechanism[1].
dBAZ2B (0.25 μM; 4 h) depletes PT117, SESD1, and BBS7 proteins (an effect linked to BAZ2A bromodomain inhibition) and does not significantly alter BAZ2A levels in this proteomic assay[1].
dBAZ2B (0.25 μM; 4 h) selectively degrades BAZ2B and increases BAZ2A levels in MM1S cells, demonstrating its cell-line-independent selectivity[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 3104449-58-0
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Molecular Weight 1028.25
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Formula C55H66FN11O6S
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SMILES
CC1=C(SC=N1)C2=CC(OC[C@@H]3CC[C@H](CC3)COCC4=NC(C5=CN(N=C5)C)=C(N4CCC6=CN(N=C6)C)C7=CC=C(C=C7)C#N)=C(C=C2)CNC([C@@H]8C[C@H](CN8C([C@H](C(C)(C)C)NC(C9(CC9)F)=O)=O)O)=O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)