Discovery of Potent Deuterated Compounds As Potential KRAS Inhibitors in Cancer Therapy
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The disclosure in this Patent Highlight describes a new class of deuterated compounds that bind directly to KRAS and block its activity. These exemplary deuterated compounds are potentially useful as pharmaceuticals that may possess desirable properties, including bioavailability, stability, and therapeutic index. This may have significant influence in drugs absorption, distribution, metabolism, excretion, and half-life when administered to a human or animal. The replacement of C-H with C-D increases the kinetic isotope effect, which makes the C-D bond up to ∼10 times stronger than the C-H bond.
KRAS Mutation Detection with (2,4)-4-[F]FGln for Noninvasive PDAC Diagnosis.
Liu S, Liu F, Hou X, Zhang Q, Ren Y, Zhu H Mol Pharm. 2024; 21(4):2034-2042.
PMID: 38456403 PMC: 10989612. DOI: 10.1021/acs.molpharmaceut.4c00082.