Evidence map›Paper›PMID 41341056›Full record

ArticleACS central science2025

SynLlama: Generating Synthesizable Molecules and Their Analogs with Large Language Models.

Kunyang Sun, Dorian Bagni, Joseph M Cavanagh, Yingze Wang, Jacob M Sawyer, Bo Zhou, Andrew Gritsevskiy, Oufan Zhang, Teresa Head-Gordon

Abstract read
In one paragraph

Article in ACS central science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. SynthesizabilityChemical science · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Kunyang Sun†Kenneth S. Pitzer Theory Center and Department of Chemistry, ‡Department of Bioengineering, and §Department of Chemical and Biomolecular Engineering, University of California, Berkeley, California 94720, United States.ORCID https://orcid.org/0000-0001-6472-1665
Dorian Bagni†Kenneth S. Pitzer Theory Center and Department of Chemistry, ‡Department of Bioengineering, and §Department of Chemical and Biomolecular Engineering, University of California, Berkeley, California 94720, United States.
Joseph M Cavanagh†Kenneth S. Pitzer Theory Center and Department of Chemistry, ‡Department of Bioengineering, and §Department of Chemical and Biomolecular Engineering, University of California, Berkeley, California 94720, United States.
Yingze Wang†Kenneth S. Pitzer Theory Center and Department of Chemistry, ‡Department of Bioengineering, and §Department of Chemical and Biomolecular Engineering, University of California, Berkeley, California 94720, United States.
Jacob M SawyerDepartment of Chemistry, University of Minnesota, 207 Pleasant Street SE, Minneapolis, Minnesota 55455, United States.
Bo ZhouDepartment of Pharmaceutical Sciences, University of Illinois Chicago, 833 S Wood St, Chicago, Illinois 60612, United States.ORCID https://orcid.org/0009-0001-5603-4221
Andrew GritsevskiyContramont Research, San Francisco, California 94158, United States.
Oufan Zhang†Kenneth S. Pitzer Theory Center and Department of Chemistry, ‡Department of Bioengineering, and §Department of Chemical and Biomolecular Engineering, University of California, Berkeley, California 94720, United States.
Teresa Head-Gordon†Kenneth S. Pitzer Theory Center and Department of Chemistry, ‡Department of Bioengineering, and §Department of Chemical and Biomolecular Engineering, University of California, Berkeley, California 94720, United States.ORCID https://orcid.org/0000-0003-0025-8987

Funding

Project 5: Pandemic Virus Helicase InhibitorsU19AI171954 · NIAID · UNIVERSITY OF MINNESOTA · PI Reuben S Harris, Fang Li · 2022 to 2026
$100.9M
NIAID NIH HHS U19 AI171954
6 · The paper itself

Abstract

Generative machine learning models for exploring chemical space have shown immense promise, but many molecules that they generate are too difficult to synthesize, making them impractical for further investigation or development. In this work, we present a novel approach by fine-tuning Meta's Llama3 Large Language Models (LLMs) to create SynLlama, which generates full synthetic pathways made of commonly accessible building blocks and robust organic reaction templates. SynLlama explores a large synthesizable space using significantly less data and offers strong performance in both forward and bottom-up synthesis planning compared to other state-of-the-art methods. We find that SynLlama, even without training on external building blocks, can effectively generalize to unseen yet purchasable building blocks, meaning that its reconstruction capabilities extend to a broader synthesizable chemical space than those of the training data. We also demonstrate the use of SynLlama in a pharmaceutical context for synthesis planning of analog molecules and hit expansion leads for proposed inhibitors of target proteins, offering medicinal chemists a valuable tool for discovery.

Identifiers

PMID41341056
PMCPMC12670306

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.