SmartChemist─Simplifying Communication About Organic Chemical Structures

Communication between collaborators of different (scientific) backgrounds can be difficult in any interdisciplinary work. Frequently used language of different disciplines can be partially unknown or sometimes even contradict each other. One example of this is knowledge about organic chemical nomenclature used by chemists. Although highly efficient, this nomenclature can be challenging to learn and confusing for scientists new to it. Today, interdisciplinary teams in chemistry often consist of a diverse range of experts, including those from biology, pharmacology, medicine, computer science, and mathematics. This can complicate communication regarding chemical structures, impeding a productive work environment and potentially introducing errors. To address this issue, we present a new web tool called SmartChemist. This tool enables users to upload molecular files or enter SMILES of molecules. It then displays the names of identified substructures, including cyclic substructures, functional groups, and common biologically relevant organic molecules. It utilizes a database of over 40,000 patterns that have been carefully generated for this purpose, and it only shows the most specific substructures found while enabling novices to inquire about all substructures found.

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Publication Details

Journal
Journal of Chemical Information and Modeling
Published
2025-06-09
DOI
https://doi.org/10.1021/acs.jcim.5c00599
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
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article

SmartChemist─Simplifying Communication About Organic Chemical Structures

Uschi Dolfus, Patrick Penner, Torben Gutermuth, Jochen Sieg et al.
Journal of Chemical Information and Modeling
Computational Drug Discovery Methods
article

SmartChemist─Simplifying Communication About Organic Chemical Structures

Uschi Dolfus, Patrick Penner, Torben Gutermuth, Jochen Sieg, Matthias Rarey
article en

Abstract

Communication between collaborators of different (scientific) backgrounds can be difficult in any interdisciplinary work. Frequently used language of different disciplines can be partially unknown or sometimes even contradict each other. One example of this is knowledge about organic chemical nomenclature used by chemists. Although highly efficient, this nomenclature can be challenging to learn and confusing for scientists new to it. Today, interdisciplinary teams in chemistry often consist of a diverse range of experts, including those from biology, pharmacology, medicine, computer science, and mathematics. This can complicate communication regarding chemical structures, impeding a productive work environment and potentially introducing errors. To address this issue, we present a new web tool called SmartChemist. This tool enables users to upload molecular files or enter SMILES of molecules. It then displays the names of identified substructures, including cyclic substructures, functional groups, and common biologically relevant organic molecules. It utilizes a database of over 40,000 patterns that have been carefully generated for this purpose, and it only shows the most specific substructures found while enabling novices to inquire about all substructures found.

Journal of Chemical Information and ModelingVol. 65(17)
Universität Hamburg (DE)
Openalex Percentile: Top 86%
Computational Drug Discovery Methods
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SmartChemist─Simplifying Communication About Organic Chemical Structures — Uschi Dolfus, Patrick Penner, et al. · Journal of Chemical Information and Modeling (2025) | TGRS Research Map | TGRS