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[ CAS No. 66338-96-3 ] {[proInfo.proName]}

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Chemical Structure| 66338-96-3
Chemical Structure| 66338-96-3
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Jonathan M. Stokes ; Kevin Yang ; Kyle Swanson , et al. DOI: PubMed ID:

Abstract: Due to the rapid emergence of antibiotic-resistant bacteria, there is a growing need to discover new antibiotics. To address this challenge, we trained a deep neural network capable of predicting molecules with antibacterial activity. We performed predictions on multiple chemical libraries and discovered a molecule from the Drug Repurposing Hub—halicin—that is structurally divergent from conventional antibiotics and displays bactericidal activity against a wide phylogenetic spectrum of pathogens including Mycobacterium tuberculosis and carbapenem-resistant Enterobacteriaceae. Halicin also effectively treated Clostridioides difficile and pan-resistant Acinetobacter baumannii infections in murine models. Additionally, from a discrete set of 23 empirically tested predictions from >107 million molecules curated from the ZINC15 database, our model identified eight antibacterial compounds that are structurally distant from known antibiotics. This work highlights the utility of deep learning approaches to expand our antibiotic arsenal through the discovery of structurally distinct antibacterial molecules.

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Product Details of [ 66338-96-3 ]

CAS No. :66338-96-3 MDL No. :MFCD00062754
Formula : C5H5N3O3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 187.18 Pubchem ID :-
Synonyms :

Safety of [ 66338-96-3 ]

Signal Word:Danger Class:4.1,6.1
Precautionary Statements:P240-P210-P241-P280-P370+P378-P501-P261-P270-P271-P264-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405 UN#:2926
Hazard Statements:H228-H301+H311+H331-H315-H319 Packing Group:
GHS Pictogram:
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