iBRD4-BD1
Modify Date: 2024-04-05 23:01:50
iBRD4-BD1 structure
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Common Name | iBRD4-BD1 | ||
|---|---|---|---|---|
| CAS Number | 2839318-17-9 | Molecular Weight | 521.58 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C29H30F3N5O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of iBRD4-BD1iBRD4-BD1 is selective BRD4 bromodomain inhibitor. iBRD4-BD1 has inhibition activity for BRD4 bromodomain with an IC50 value of 12 nM. iBRD4-BD1 can be used for the research of inflammation and oncology[1]. |
| Name | iBRD4-BD1 |
|---|
| Description | iBRD4-BD1 is selective BRD4 bromodomain inhibitor. iBRD4-BD1 has inhibition activity for BRD4 bromodomain with an IC50 value of 12 nM. iBRD4-BD1 can be used for the research of inflammation and oncology[1]. |
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| Related Catalog | |
| In Vitro | iBRD4-BD1 has affinity and selectivity for the BET-family BRD4-BD1 with an IC50 value of 12 nM[1]. iBRD4-BD1 has affinity and selectivity for the BET-family BRD4-BD2, BRD3-BD1, BRD3-BD2, BRD2-BD1 and BRD2-BD2 with IC50 values of 16 μM, 1.0 μM , 75 μM , 280 nM and 7.1 μM, respectively[1]. iBRD4-BD1 (0-50 μM; 72 h) has cytotoxicity with an EC50 value of 2.3 μM in MM.1S cells[1]. Western Blot Analysis[1] Cell Line: MM.1S cells Concentration: 0-300 pM Incubation Time: 1 h Result: Prevented the denaturation of BRD4 in a dose-dependent manner and showed stabilization of BRD4 at concentrations above 3 nM. Cell Cytotoxicity Assay[1] Cell Line: MM.1S cells Concentration: 0-50 μM Incubation Time: 72 h Result: Showed cytotoxicity with an EC50 value of 2.3 μM in MM.1S cells. |
| Molecular Formula | C29H30F3N5O |
|---|---|
| Molecular Weight | 521.58 |