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KY-2 is an orally bioavailable small molecule inhibitor of the eukaryotic initiation factor 4A (eIF4A) RNA helicase, currently in preclinical development by Keye Life Sciences (Kaiyue Biotech). eIF4A is a key component of the eIF4F complex, which is responsible for the recruitment of ribosomes to mRNA. By inhibiting eIF4A, KY-2 disrupts the translation of mRNAs with complex 5' untranslated regions (UTRs), which often encode potent oncogenes and survival factors such as MYC, BCL2, and cyclin D1. This mechanism is particularly relevant for treating late-stage solid tumors and gastrointestinal cancers where dysregulated protein synthesis drives tumor progression and resistance.
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