Programmable Modular Assembly of Homochiral Ir(III)‐Metallohelices to Reverse Metallodrug Resistance by Inhibiting CDK1

Drug resistance is a major cause of cancer recurrence and poor prognosis. The innovative design and synthesis of inhibitors to target drug‐resistance‐specific proteins is highly desirable. However, challenges remain in precisely adjusting their conformation and stereochemistry to adapt the chiral regions of target proteins. Herein, using a stepwise programmable modular assembly approach, we precisely engineered two pairs of homochiral dinuclear Ir(III) metallohelices (Λ2S4‐Hbpy and Δ2R4‐Hbpy, Δ2S4‐Hbpy and Λ2R4‐Hbpy) functionalized with flexible dithiourea linkages. The resulting homochiral metallohelices exhibited significant chirality‐dependent photocytotoxicities, and the enhanced structural compatibility ofΔ2S4‐Hbpywith the target cyclin‐dependent kinase 1 (CDK1) contributed to its superior photodynamic therapy efficacy, achieving an outstanding photocytotoxicity index (PI) value of 2.3×104. Interestingly, emerging as a critical mediator in the development of oxaliplatin resistance, CDK1 targeting by Δ2S4‐Hbpyachieved enhanced cellular uptake, anticancer activity, and oncosis‐mediated cell death in oxaliplatin‐resistant HCT8/L cells. Mechanistic investigations, including proteomic profiling and CDK1 gene silencing, confirmed the pivotal role of chirality‐selective CDK1 targeting in reversing metallodrug resistance. This study introduces a promising platform for constructing and customizing flexible metallohelices with precise conformation and stereochemistry to target drug‐resistance‐specific proteins, offering innovative insights into the designability of metallodrugs to overcome drug resistance.