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April 5, 2026Cancer Research0 citations

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

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QXQingbo XuHYHailong YangYWYing Wang

Key Points

  • The study aims to enhance the identification of CRBN molecular glue binders through a diverse library and AI-driven methods.
  • Constructed a CRBN molecular glue-biased library with over 40 validated binders.
  • Introduced novel fragments through an AI-based molecular generation model for increased diversity.
  • Conducted high-throughput screening to evaluate the library's efficiency in identifying binders.
  • The library successfully identified unique CRBN-substrate ternary binders.
  • Several degraders with novel scaffolds were discovered, indicating high potential for optimization.

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.

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Cite This Study

Xu et al. (2026) studied this question.

synapsesocial.com/papers/69d1fca7a79560c99a0a2428https://doi.org/10.1158/1538-7445.am2026-6402
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