Not Every Hit‐Identification Technique Works on 1‐Deoxy‐ d ‐Xylulose 5‐Phosphate Synthase (DXPS): Making the Most of a Virtual Screening Campaign

Abstract: In this work, we demonstrate how important it is to investigate not only on‐target activity but to keep antibiotic activity against critical pathogens in mind. Since antimicrobial resistance is spreading in bacteria such as Mycobacterium tuberculosis, investigations into new targets are urgently needed. One promising new target is 1‐deoxy‐d‐xylulose 5‐phosphate synthase (DXPS) of the 2‐C‐methyl‐d‐erythritol 4‐phosphate (MEP) pathway. We have recently solved the crystal structure of truncated M. tuberculosis DXPS and used it to perform a virtual screening in collaboration with Atomwise Inc. using their deep convolutional neural network‐based AtomNet® platform. Of 94 virtual hit compounds only one showed interesting results in binding and activity studies. We synthesized 30 close derivatives using a straightforward synthetic route that allowed for easy derivatization. However, no improvement in activity was observed for any of the derivatives. Therefore, we tested them against a variety of pathogens and found them to be good inhibitors against Escherichia coli.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Not Every Hit‐Identification Technique Works on 1‐Deoxy‐ d ‐Xylulose 5‐Phosphate Synthase (DXPS): Making the Most of a Virtual Screening Campaign ; day:14 ; month:04 ; year:2023 ; extent:10
ChemMedChem ; (14.04.2023) (gesamt 10)

Urheber
Johannsen, Sandra
Gierse, Robin M.
Olshanova, Aleksandra
Smerznak, Ellie
Laggner, Christian
Eschweiler, Lea
Adeli, Zahra
Hamid, Rawia
Alhayek, Alaa
Reiling, Norbert
Haupenthal, Jörg
Hirsch, Anna K. H.

DOI
10.1002/cmdc.202200590
URN
urn:nbn:de:101:1-2023041515132630470445
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:58 MESZ

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