PBRM1-BD2-IN-6
PBRM1-BD2-IN-6 is a potent PBRM1 bromodomain inhibitor with an IC50 value of 0.22 μM. PBRM1-BD2-IN-6 shows antiproliferation activity. PBRM1-BD2-IN-6 has the potential for the research of PBRM1-dependent cancer.
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- CAS. Nr.: 2819989-67-6
- Formel: C16H15ClN2O
- Molecular Weight:286.76
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biologische Aktivität
Beschreibung
IC50 & Target
IC50: 0.22 nM (PBRM1-BD2)[1]
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| LNCaP | IC50 |
0.66 μM
Compound: 25
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Cytotoxicity against human LNCaP cells assessed as inhibition of cell growth measured after 7 days with compound replacement for every 48 hrs by celltiter-glo assay
Cytotoxicity against human LNCaP cells assessed as inhibition of cell growth measured after 7 days with compound replacement for every 48 hrs by celltiter-glo assay
|
[PMID: 36227159] |
In Vitro
PBRM1-BD2-IN-6 (compound 25) (0.1, 1, 10 μM; 5 days) shows antiproliferation activity with IC50 values of 0.66, 0.77, 0.32 μM for LNCaP, PC3, HEK293T cells, respectively[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. .
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Cell Line:LNCaP, PC3, HEK293T cells
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Concentration:0.1, 1, 10 μM
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Incubation Time:5 days
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Result:Inhibited the cell growth with IC50 values of 0.66, 0.77, 0.32 µM for LNCaP, PC3, HEK293T cells, respectively.
Chemical Information
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CAS. Nr. 2819989-67-6
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Molecular Weight 286.76
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Formel C16H15ClN2O
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SMILES
O=C1NC(C2=CC=CC(C)=C2C)NC3=C1C(Cl)=CC=C3
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)