Name | MI-1061 |
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Description | MI-1061 is a potent, orally bioavailable, and chemically stable MDM2 (MDM2-p53 interaction) inhibitor (IC50=4.4 nM; Ki=0.16 nM). MI-1061 potently activates p53, induces apoptosis, and has anti-tumor activity[1]. |
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Related Catalog | |
Target |
IC50: 4.4 nM (MDM2)[1] Ki: 0.16 nM (MDM2) |
In Vitro | MI-1061 achieves IC50=100 and 250 nM in the SJSA-1 and HCT-116 p53+/+ cell lines, respectively, and has IC50>10000 nM in the p53 knockout cell line HCT-116 p53–/–cell line[1]. |
In Vivo | MI-1061 is capable of achieving tumor regression in the SJSA-1 xenograft tumor model in mice with oral administration[1]. |
References |
Molecular Formula | C30H26Cl2FN3O4 |
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Molecular Weight | 582.45 |