Chemical Structure : Idasanutlin
CAS No.: 1229705-06-9
Catalog No.: PC-25429Not For Human Use, Lab Use Only.
Idasanutlin (RG7388) is a potent and selective p53-MDM2 inhibitor with IC50 of 6 nM in HTRF binding assays, inhibits wt-p53 cancer cell lines (SJSA1, RKO, HCT116) with mean IC50 of 0.03 uM.
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Idasanutlin (RG7388) is a potent and selective p53-MDM2 inhibitor with IC50 of 6 nM in HTRF binding assays, inhibits wt-p53 cancer cell lines (SJSA1, RKO, HCT116) with mean IC50 of 0.03 uM.
Idasanutlin (RG7388) shows >300-fold selective over mutant p53 cell lines (SW480, MDA-MB435).
Idasanutlin (RG7388) effectively activated the p53 pathway in SJSA1 cells and induced tumor growth inhibition (TGI) in correlative xenografts in nude mice .
Idasanutlin (RG7388) has demonstrated the ability to activate apoptosis and induce tumor stasis with continuous treatment.
M.Wt | 616.49 | |
Formula | C31H29Cl2F2N3O4 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
4-((2R,3S,4R,5S)-3-(3-Chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-3-methoxybenzoic acid |
1. Ding Q, et al. J Med Chem. 2013 Jul 25;56(14):5979-83.
2. Higgins B, et al. Clin Cancer Res. 2014 Jul 15;20(14):3742-52.
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