INCB054329
Modify Date: 2025-08-25 22:54:52
INCB054329 structure
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Common Name | INCB054329 | ||
|---|---|---|---|---|
| CAS Number | 1628607-64-6 | Molecular Weight | 348.36 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C19H16N4O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of INCB054329INCB054329 is a potent BET inhibitor. |
| Name | INCB054329 |
|---|
| Description | INCB054329 is a potent BET inhibitor. |
|---|---|
| Related Catalog | |
| Target |
BET[1] |
| In Vitro | INCB054329 is a bromodomain and extra-terminal motif (BET) inhibitor[1]. INCB054329 inhibits binding of BRD2, BRD3 and BRD4 to an acetylated histone H4 peptide with low nanomolar potency. In myeloma cell lines, treatment with INCB054329 inhibits expression of c-MYC and induced HEXIM1. The majority of myeloma, AML, and lymphoma cell lines tested are growth inhibited by INCB054329 with potencies less than 200 nM. Selectivity is seen when compared with nontransformed cells as the potency for growth inhibition of IL-2 stimulated T-cells from normal donors is greater than 1300 nM. Cell cycle analysis reveals treatment-induced G1 arrest. Furthermore in both AML and lymphoma cell lines, INCB054329 induces apoptosis consistent with increased expression of pro-apoptotic regulators[2]. |
| In Vivo | Oral administration of INCB054329 inhibits tumor growth in several models of hematologic cancers. In the MM1.S multiple myeloma xenograft model, inhibition of tumor growth is correlated with reduction of c-MYC levels. PK-PD analysis shows c-MYC suppression is associated with an IC50 value of less than 100 nM in vivo[2]. |
| References |
[2]. Phillip CC Liu, et al. Abstract 3523: Discovery of a novel BET inhibitor INCB054329. |
| Molecular Formula | C19H16N4O3 |
|---|---|
| Molecular Weight | 348.36 |
| InChIKey | XYLPKCDRAAYATL-OAHLLOKOSA-N |
| SMILES | Cc1noc(C)c1-c1ccc2[nH]c(=O)n3c2c1OCC3c1ccccn1 |
| Storage condition | 2-8℃ |