药物发现
小分子
DNA
前列腺癌
化学
癌症
癌细胞
计算生物学
免疫系统
癌症研究
组合化学
生物
生物化学
遗传学
作者
Francesca Migliorini,Andrea Ciamarone,Sheila Dakhel Plaza,Tony Georgiev,Marta Mascellani,Emanuela Sabato,Giulio Vistoli,Ilaria Biancofiore,Nicholas Favalli,Emanuele Puca,Sebastian Oehler,Dario Neri,Samuele Cazzamalli
标识
DOI:10.1002/advs.202505351
摘要
Abstract DNA‐encoded chemical libraries (DELs) are powerful tools for drug discovery, enabling the high‐throughput screening of vast libraries of small molecules against target proteins of pharmaceutical interest. Here, the synthesis of two new DELs, named FM‐DEL1 and FM‐DEL2, including 7′710 and 5′697’690 compounds, respectively is described. These libraries are constructed by installing one or two sets of building blocks on a phenylalanine central scaffold. FM‐DELs are screened against markers of prostate cancer, and renal cell carcinoma, and against an immunological target expressed on the surface of natural killer cells. Highly potent and selective binders with affinity constants in the nanomolar range are obtained from DEL screenings against those targets. Small‐molecule ligands against tumor‐associated antigens are used to develop small‐molecule radiopharmaceuticals that selectively accumulate at cancer sites after systemic administration.
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