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MI-2
Cat No.
CEI-1421
Description
MI-2 is an inhibitor of MALT1 with IC50 value of 5.84 μM.
Product Overview
MI-2 is a Menin-MLL inhibitor with IC50 value of 0.45 μM. Mixed-lineage leukemia (MLL) is a common target of chromosomal translocations in patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). The leukemogenic activity of MLL fusion proteins is dependent on their direct interaction with menin, which is a tumor suppressor that directly controls cell growth in endocrine organs. MI-2 is a Menin-MLL inhibitor. MI-2 bound to the wild-type menin but didn't bind M278K and Y323K menin mutants. In HEK293 cells transfected with Flag-MLL-AF9, MI-2 effectively inhibited the menin-MLL-AF9 interaction without affecting the expression level of menin and MLL-AF9.In mouse bone marrow cells (BMC) transduced with MLL-AF9 and MLL-ENL, MI-2 blocked proliferation of BMC with GI50 value of about 5 μM. Also, MI-2 inhibited colony formation in BMC transduced with MLL-AF9.In a series of human MLL leukemia cell lines, MI-2 significantly inhibited translocation in a dose dependant way.
CAS No.
1271738-62-5
Molecular Weight
375.55
Purity
0.9988
Storage
Store at -20°C
Synonyms
Menin-MLL inhibitor 2; Thieno[2,3-d]pyrimidine, 4-[4-(4,5-dihydro-5,5-dimethyl-2-thiazolyl)-1-piperazinyl]-6-propyl-
Targets
MLL
IC50
5.84 μM
Molecular Formula
C18H25N5S2
Chemical Name
4-[4-(5,5-dimethyl-4H-1,3-thiazol-2-yl)piperazin-1-yl]-6-propylthieno[2,3-d]pyrimidine
Solubility
Soluble in DMSO > 10 mM
Shipping Conditions
Evaluation sample solution: ship with blue ice. All other available size: ship with RT, or blue ice upon request
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