
Ziftomenib
CAS No. 2134675-36-6
Ziftomenib( —— )
Catalog No. M35131 CAS No. 2134675-36-6
Ziftomenib (KO-539) is an inhibitor of menin-MLL interaction with antitumor activity, suitable for leukemia research.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 175 | Get Quote |
![]() ![]() |
5MG | 272 | Get Quote |
![]() ![]() |
10MG | 372 | Get Quote |
![]() ![]() |
25MG | 592 | Get Quote |
![]() ![]() |
50MG | 908 | Get Quote |
![]() ![]() |
100MG | 1314 | Get Quote |
![]() ![]() |
200MG | 1773 | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameZiftomenib
-
NoteResearch use only, not for human use.
-
Brief DescriptionZiftomenib (KO-539) is an inhibitor of menin-MLL interaction with antitumor activity, suitable for leukemia research.
-
DescriptionZiftomenib (KO-539) is an orally active menin-MLL interaction inhibitor with antitumor activities (WO2017161028A1, compound 151).
-
In VitroThe 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.
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorHistone Methyltransferase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2134675-36-6
-
Formula Weight717.871
-
Molecular FormulaC33H42F3N9O2S2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (139.30 mM; Ultrasonic )
-
SMILESCNc1nc(NC2CCN(Cc3ccc4n(C[C@H](C)N5CCN(CC5)S(C)(=O)=O)c(cc4c3C)C#N)CC2)c2cc(CC(F)(F)F)sc2n1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Tao Wu, et al. Substituted inhibitors of menin-mll and methods of use. WO2017161028A1.
molnova catalog



related products
-
Soyasaponin Aa
Soyasaponin Aa and soyasaponin Ab dose-dependently markedly inhibit adipocyte differentiation and expression of various adipogenic marker genes, through the downregulation of the adipogenesis-related transcription factors PPARγ and C/EBPα± in 3T3-L1 adipocytes.
-
2-Fluoroadenosine
2-Fluoroadenosine is a potent inhibitor of lymphocyte-mediated cytolysis.
-
Notoginsenoside Fe
Notoginsenoside Fe is a natural compound isolated from Panax japlcus var.