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MACAW: An Accessible Tool for Molecular Embedding and Inverse Molecular Design.
Blay, Vincent; Radivojevic, Tijana; Allen, Jonathan E; Hudson, Corey M; Garcia Martin, Hector.
Affiliation
  • Blay V; Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
  • Radivojevic T; Biofuels and Bioproducts Division, DOE Joint BioEnergy Institute, Emeryville, California 94608, United States.
  • Allen JE; Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
  • Hudson CM; Biofuels and Bioproducts Division, DOE Joint BioEnergy Institute, Emeryville, California 94608, United States.
  • Garcia Martin H; DOE Agile BioFoundry, Emeryville, California 94608, United States.
J Chem Inf Model ; 62(15): 3551-3564, 2022 08 08.
Article in En | MEDLINE | ID: mdl-35857932
The growing capabilities of synthetic biology and organic chemistry demand tools to guide syntheses toward useful molecules. Here, we present Molecular AutoenCoding Auto-Workaround (MACAW), a tool that uses a novel approach to generate molecules predicted to meet a desired property specification (e.g., a binding affinity of 50 nM or an octane number of 90). MACAW describes molecules by embedding them into a smooth multidimensional numerical space, avoiding uninformative dimensions that previous methods often introduce. The coordinates in this embedding provide a natural choice of features for accurately predicting molecular properties, which we demonstrate with examples for cetane and octane numbers, flash points, and histamine H1 receptor binding affinity. The approach is computationally efficient and well-suited to the small- and medium-size datasets commonly used in biosciences. We showcase the utility of MACAW for virtual screening by identifying molecules with high predicted binding affinity to the histamine H1 receptor and limited affinity to the muscarinic M2 receptor, which are targets of medicinal relevance. Combining these predictive capabilities with a novel generative algorithm for molecules allows us to recommend molecules with a desired property value (i.e., inverse molecular design). We demonstrate this capability by recommending molecules with predicted octane numbers of 40, 80, and 120, which is an important characteristic of biofuels. Thus, MACAW augments classical retrosynthesis tools by providing recommendations for molecules on specification.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Histamine H1 / Octanes Type of study: Prognostic_studies Language: En Journal: J Chem Inf Model Journal subject: INFORMATICA MEDICA / QUIMICA Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Histamine H1 / Octanes Type of study: Prognostic_studies Language: En Journal: J Chem Inf Model Journal subject: INFORMATICA MEDICA / QUIMICA Year: 2022 Type: Article Affiliation country: United States