Algorithm-driven activity-directed expansion of a series of antibacterial quinazolinones
Author:
Affiliation:
1. School of Chemistry, University of Leeds, Leeds, LS2 9JT, UK
2. Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK
3. School of Molecular and Cellular Biology, University of Leeds, Leeds, LS2 9JT, UK
Abstract
Funder
University of Leeds
Engineering and Physical Sciences Research Council
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01404A
Reference34 articles.
1. Activity‐Directed Synthesis: A Flexible Approach for Lead Generation
2. Synthetic fermentation of bioactive molecules
3. Synthetic fermentation of bioactive non-ribosomal peptides without organisms, enzymes or reagents
4. Synthetic fermentation of β-peptide macrocycles by thiadiazole-forming ring-closing reactions
5. Antibiotic Discovery with Synthetic Fermentation: Library Assembly, Phenotypic Screening, and Mechanism of Action of β-Peptides Targeting Penicillin-Binding Proteins
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1. Synthesis, antibacterial evaluation, crystal structure determination, hirshfeld surface analysis and density functional theory analysis of novel 3-amino-2-(2-thienyl)-4(3H)-quinazolinone;Journal of Molecular Structure;2024-11
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