Ziftomenib
Modify Date: 2024-01-02 18:21:07
Ziftomenib structure
|
Common Name | Ziftomenib | ||
|---|---|---|---|---|
| CAS Number | 2134675-36-6 | Molecular Weight | 717.87 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C33H42F3N9O2S2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of ZiftomenibZiftomenib is a menin-MLL interaction inhibitor with antitumor activities (WO2017161028A1, compound 151)[1]. |
| Name | Ziftomenib |
|---|
| Description | Ziftomenib is a menin-MLL interaction inhibitor with antitumor activities (WO2017161028A1, compound 151)[1]. |
|---|---|
| Related Catalog | |
| In Vitro | The mixed-lineage leukemia (MLL) protein is a histone methyltransferase critical for the epigenetic regulation of gene transcription. Many acute leukemias, including acute myeloblastic leukemia (AML), acute lymphoblastic leukemia (ALL) and mixed-lineage leukemia (MLL), are characterized by the presence of chimeric MLL fusion proteins that result from chromosomal translocations of the MLL gene located at chromosome 11, band q23 (11q23). MLL fusion proteins lack the original histone methyltransferase activity of the C-terminus of MLL and gain the ability to regulate transcription of numerous oncogenes, including HOX and MEIS1, resulting in increased cell proliferation and decreased cell differentiation, ultimately leading to leukemogenesis[1]. |
| References |
[1]. Tao Wu, et al. Substituted inhibitors of menin-mll and methods of use. WO2017161028A1. |
| Molecular Formula | C33H42F3N9O2S2 |
|---|---|
| Molecular Weight | 717.87 |