Abstract 6402: Identification of novel CRBN molecular glue ternary binders from a highly diverse CRBN MG library

Abstract High-throughput screening (HTS) of cereblon (CRBN) molecular glue (MG)-biased libraries remains a key strategy for proof-of-concept studies and hit identification against emerging targets. Because the CRBN binding pocket and its induced interface can adopt multiple conformations, and the substrate binding pocket is often unpredictable at the early stages of discovery, the structural diversity of both CRBN binders and substrate-recognition motifs is crucial to screening efficiency.In this work, we constructed a high-quality, CRBN MG-biased library derived from more than 40 validated CRBN binders. To further enhance chemical diversity, we introduced novel fragments using a tailored AI-based molecular generation model, designed to maximize variations in substrate-binding motifs. HTS case studies demonstrated that this library effectively identified CRBN-substrate ternary binders and degraders with unique scaffolds, representing promising starting points for further optimization. Citation Format: Qingbo Xu, Hailong Yang, Yongqiang Wang, Zhenyu Wu, Hongbo Zhang. Identification of novel CRBN molecular glue ternary binders from a highly diverse CRBN MG library [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6402.

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Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6402
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
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article

Abstract 6402: Identification of novel CRBN molecular glue ternary binders from a highly diverse CRBN MG library

H. Zhang, Hailong Yang, Qingbo Xu, Zhenyu Wu
Cancer Research
Protein Degradation and Inhibitors
article

Abstract 6402: Identification of novel CRBN molecular glue ternary binders from a highly diverse CRBN MG library

H. Zhang, Hailong Yang, Qingbo Xu, Zhenyu Wu
article en

Abstract

Abstract High-throughput screening (HTS) of cereblon (CRBN) molecular glue (MG)-biased libraries remains a key strategy for proof-of-concept studies and hit identification against emerging targets. Because the CRBN binding pocket and its induced interface can adopt multiple conformations, and the substrate binding pocket is often unpredictable at the early stages of discovery, the structural diversity of both CRBN binders and substrate-recognition motifs is crucial to screening efficiency.In this work, we constructed a high-quality, CRBN MG-biased library derived from more than 40 validated CRBN binders. To further enhance chemical diversity, we introduced novel fragments using a tailored AI-based molecular generation model, designed to maximize variations in substrate-binding motifs. HTS case studies demonstrated that this library effectively identified CRBN-substrate ternary binders and degraders with unique scaffolds, representing promising starting points for further optimization. Citation Format: Qingbo Xu, Hailong Yang, Yongqiang Wang, Zhenyu Wu, Hongbo Zhang. Identification of novel CRBN molecular glue ternary binders from a highly diverse CRBN MG library [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6402.

Cancer ResearchVol. 86(7_Supplement)
Wilmington University (US)
Openalex Percentile: Top 22%
Protein Degradation and Inhibitors
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