PROTAC BRD9 Degrader-10
PROTAC BRD9 Degrader-10 is a PROTAC degrader targeting BRD9, with an IC50 of 2.97 μM against BRD9. PROTAC BRD9 Degrader-10 induces BRD9 degradation via the ubiquitin-proteasome system by recruiting the VHL E3 ubiquitin ligase. PROTAC BRD9 Degrader-10 reduces the viability and inhibits the proliferation of myeloid leukemia cells. PROTAC BRD9 Degrader-10 is applicable for the research of acute myeloid leukemia.
(Pink: BRD9 ligand (HY-181950); Blue: VHL ligand (HY-125845); Black: linker).
For research use only. We do not sell to patients.
- Formula: C50H62N10O7S
- Molecular Weight:947.16
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All PROTACs Isoforms
More
Biological Activity
|
BRD9 2.97 μM (IC50) |
VHL |
PROTAC BRD9 Degrader-10 (compound 2) (1-25 μM; 48 h) induces dose-dependent BRD9 degradation in U937 cells[1].
PROTAC BRD9 Degrader-10 (1-25 μM; 48 h) suppresses U937 cell viability in a dose-dependent manner[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:Human acute myeloid leukemia U937 cells
-
Concentration:1, 5 ,10, 25 μM
-
Incubation Time:48 h
-
Result:Induced dose-dependent degradation of BRD9.
-
Cell Line:Human acute myeloid leukemia U937 cells
-
Concentration:1, 5 ,10, 25 μM
-
Incubation Time:48 h
-
Result:Significantly reduced U937 cell viability at 25 μM and 10 μM.
Maintained viability near control levels at 5 μM and 1 μM.
Chemical Information
-
Molecular Weight 947.16
-
Formula C50H62N10O7S
-
SMILES
O=C(NC1=CC=CC(NC2=NC3=CC=CC=C3N4C2=NN=C4CC)=C1)CCCCCCOCCOCC(N[C@@H](C(C)(C)C)C(N5[C@H](C(NCC6=CC=C(C7=C(C)N=CS7)C=C6)=O)C[C@@H](O)C5)=O)=O
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
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)