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Solubility: H2O : 33
Methoxy-X04 retains in vitro binding affinity for amyloid beta (Abeta) fibrils (Ki = 26
inhibits UDP-glucuronosyltransferase (UGT) isoforms UGT1A6 and UGT2B7 with immunosuppressive effects
PubMed Central PMCID: PMC4468711
35 μM for human PPARα
MI-2 - Menin-MLL Inhibitor. CAS# 1271738-62-5 60033 Solubility: H2O : 33MI 2, CAS No. 1271738 62 5, is a potent and specific Menin MLL inhibitor with an IC50 ~446 nM. It specifically binds to Menin and inhibits Menins interaction with MLL fusion proteins in cells. It can effectively reverse MLL fusion proteinmediated leukemic transformation by downregulating the expression of target genes downstream of MLL fusion protein oncogenic activity. MI 2 is a new tool for better understanding MLL mediated leukemogenesis and
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