Journal
ACS MEDICINAL CHEMISTRY LETTERS
Volume 8, Issue 10, Pages 1116-1121Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsmedchemlett.7b00342
Keywords
Mutant IDHI; inhibition of 2-HG production; in vivo anticancer activity; brain penetration; clinical candidate
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Inhibition of mutant IDH1 is being evaluated clinically as a promising treatment option for various cancers with hotspot mutation at Are). Having identified an allosteric, induced pocket of IDH1(R132H), we have explored 3pyrimidin-4-yl-oxazolidin-2-ones as mutant IDH1 inhibitors for in vivo modulation of 2-HG production and potential brain penetration. We report here optimization efforts toward the identification of clinical candidate IDH305 (13), a potent and selective mutant IDH1 inhibitor that has demonstrated brain exposure in rodents. Preclinical characterization of this compound exhibited in vivo correlation of 2 -HG reduction and efficacy in a patient -derived IDH1 mutant xenograft tumor model. IDH305 (13) has progressed into human clinical trials for the treatment of cancers with IDH1 mutation.
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