Chemical Structure : MK-8242
货号: PC-60262Not For Human Use, Lab Use Only.
A potent, orally bioavailable, small-molecule inhibitor of HDM2/p53 protein-protein interaction.
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A potent, orally bioavailable, small-molecule inhibitor of HDM2/p53 protein-protein interaction; stabilizes the tumor suppressor TP53 and induces growth arrest or apoptosis downstream of TP53 induction; has an IC50 of 70 nM for TP53 wild-type cell lines versus >10 uM for TP53 mutant cell lines.
Blood Cancer
Phase 1 Clinical
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外观性状 | Solid | |
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Solubility |
10 mM in DMSO |
1. Kang MH, et al. Pediatr Blood Cancer. 2016 Oct;63(10):1744-52.
2. Cancer Discov. 2017 May;7(5):451. doi: 10.1158/2159-8290.CD-RW2017-047.
3. Wagner AJ, et al. J Clin Oncol. 2017 Apr 20;35(12):1304-1311.
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