High-Throughput Virtual Screening of Compounds with Electrophilic Fragments for New Potential Covalent Inhibitors of Bacterial Proteins-Reference-Cited by-同舟云学术

High-Throughput Virtual Screening of Compounds with Electrophilic Fragments for New Potential Covalent Inhibitors of Bacterial Proteins

Published:2022-11-14 Issue: Volume: Page:
ISSN:
Container-title:The 26th International Electronic Conference on Synthetic Organic Chemistry
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Author:

Yakovets Polina¹,Staravoitava Viktoryia²^ORCID,Faletrov Yaroslav¹²,Shkumatov Vladimir¹²

Affiliation:

1. Department of Chemistry, Belarusian State University, 14 Leningradskaya St., 220006 Minsk, Belarus

2. Research Institute for Physical Chemical Problems of the Belarusian State University, Minsk, Belarus 14 Leningradskaya St., 220030 Minsk, Belarus

Publisher

MDPI

Link

https://www.mdpi.com/2673-4583/12/1/87/pdf

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3. Interaction of Nitrobenzoxadiazole Derivatives of Piperazine and Aniline with Bovine Serum Albumine in Silico and in Vitro;Faletrov;J. Belarusian State Univ. Chem.,2021

4. Faletrov, Y.V., Staravoitava, V.A., Dudko, A.R., and Shkumatov, V.M. (2022). Application of Docking-Based Inverse High Throughput Virtual Screening to Found Phytochemical Covalent Inhibitors of SARS-CoV-2 Main Protease, NSP12 and NSP16, preprint.

5. Mycobacterium tuberculosis β-Ketoacyl Acyl Carrier Protein Synthase III (mtFabH) Assay: Principles and Method;Champney;New Antibiotic Targets. Methods In Molecular Medicine™,2008

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