{
  "abstract": "Molecular graphs and molecular strings are two well-established molecular representations for deep learning, with complementary strengths: while graphs make atom and bond properties explicit, strings are sequential and straightforward to generate. Here, we introduce a novel molecular representation than bridges these two representations: Multichannel Atom and Topology for Chemical Representation Series (MATCHERS). In a single representation, MATCHERS encode user-defined atomic properties, explicit molecular topology, as well as bond properties, while maintaining the sequential character typical of molecular strings. In this proof-of-concept, we show that MATCHERS outperform sequential string representations (SMILES and SELFIES) for bioactivity prediction, and that they can be used for de novo molecular design. MATCHERS illustrate the untapped opportunity of explicitly encoding chemical knowledge into new molecular representations that remain compatible with deep learning.",
  "abstract_shown": true,
  "affiliations": [
    "Department of Biomedical Engineering",
    "Institute for Complex Molecular Systems (ICMS), Eindhoven University of Technology",
    "Department of Mathematics and Computer Science",
    "Freie Universität Berlin"
  ],
  "article_type": null,
  "arxiv": null,
  "author_total": 4,
  "authors": [
    {
      "affs": [
        0,
        1
      ],
      "name": "Helena Brinkmann"
    },
    {
      "affs": [
        0,
        1
      ],
      "name": "Rıza Özçelik"
    },
    {
      "affs": [
        0,
        1,
        2,
        3
      ],
      "name": "Katarina Elez"
    },
    {
      "affs": [
        0,
        1
      ],
      "name": "Francesca Grisoni"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/ec83nbnr8qyav.bib",
  "cited_by": 0,
  "doi": "10.26434/chemrxiv.15011134/v1",
  "fulltext_url": null,
  "id": "ec83nbnr8qyav",
  "issns": [],
  "landing_url": "https://chemrxiv.org/doi/full/10.26434/chemrxiv.15011134/v1",
  "language": null,
  "licence": "CC-BY",
  "licence_label": "CC BY",
  "licence_source": "journal",
  "licence_url": "https://creativecommons.org/licenses/by/4.0/",
  "metadata_licence": null,
  "native_subjects": [
    [
      "openalex",
      "1703|Computational Drug Discovery Methods"
    ]
  ],
  "openalex": "W7224003636",
  "pdf_url": null,
  "pmcid": null,
  "pmid": null,
  "published": "2026-10-27",
  "publisher": "American Chemical Society (ACS)",
  "ris": "https://research.draconitic.com/paper/ec83nbnr8qyav.ris",
  "sources": [
    {
      "first_seen": "2026-10-30T12:17:26Z",
      "native_id": "10.26434/chemrxiv.15011134",
      "source": "chemrxiv",
      "url": "https://chemrxiv.org/doi/full/10.26434/chemrxiv.15011134/v1"
    }
  ],
  "subjects": [
    {
      "field": "chemistry",
      "origin": "source:chemrxiv",
      "subfield": "general"
    }
  ],
  "title": "MATCHERS: a ‘chemistry-infused’ representation bridging molecular graphs and strings",
  "title_text": "MATCHERS: a ‘chemistry-infused’ representation bridging molecular graphs and strings",
  "type": "preprint",
  "updated_at": "2026-10-30T12:17:26Z",
  "url": "https://research.draconitic.com/paper/ec83nbnr8qyav",
  "venue": "ChemRxiv",
  "versions": []
}