Large Language Model Agent for Modular Task Execution in Drug Discovery.

Authors

Janghoon Ock, Radheesh Sharma Meda, Srivathsan Badrinarayanan, Neha S Aluru, Achuth Chandrasekhar, Amir Barati Farimani

Published in

Journal of chemical information and modeling. Volume 66. Issue 4. Pages 2055-2068. Feb 23, 2026. Epub Feb 09, 2026.

Abstract

We present a modular framework powered by large language models (LLMs) that automates and streamlines key tasks across the early stage computational drug discovery pipeline. By combining LLM reasoning with domain-specific tools, the framework performs biomedical data retrieval, literature-grounded question answering via retrieval-augmented generation, molecular generation, multiproperty prediction, property-aware molecular refinement, and 3D protein-ligand structure generation. The agent autonomously retrieves relevant biomolecular information, including FASTA sequences, SMILES representations, and literature, and answers mechanistic questions with improved contextual accuracy compared to standard LLMs. It then generates chemically diverse seed molecules and predicted 75 properties, including ADMET-related and general physicochemical descriptors, which guids iterative molecular refinement. Across two refinement rounds, the number of molecules with QED >0.6 increased from 34 to 55. The number of molecules satisfying empirical drug-likeness filters also rose; for example, compliance with the Ghose filter increased from 32 to 55 within a pool of 100 molecules. The framework also employed Boltz-2 to generate 3D protein-ligand complexes and provide rapid binding affinity estimates for candidate compounds. These results demonstrate that the approach effectively supports molecular screening, prioritization, and structure evaluation. Its modular design enables flexible integration of evolving tools and models, providing a scalable foundation for AI-assisted therapeutic discovery.

PMID:
41662220
Bibliographic data and abstract were imported from PubMed on 16 Sep 2026.

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