Structure-based drug design of an inhibitor of the SARS-CoV-2 (COVID-19) main protease using free software: a tutorial for students and scientists (Q98577324)

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Structure-based drug design of an inhibitor of the SARS-CoV-2 (COVID-19) main protease using free software: A tutorial for students and scientists

23 August 2020

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title

Structure-based drug design of an inhibitor of the SARS-CoV-2 (COVID-19) main protease using free software (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32817929%20AND%20SRC:MED&resulttype=core&format=json

23 August 2020

subtitle

A tutorial for students and scientists (English)

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23 August 2020

Maj Krumberger

2

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23 August 2020

Michael A Morris

3

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23 August 2020

Chelsea Marie T Parrocha

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23 August 2020

Adam G Kreutzer

6

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23 August 2020

James Nowick

7

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23 August 2020

author name string

James H Griffin

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23 August 2020

publication date

12 August 2020

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23 August 2020

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Creative Commons Attribution 4.0 International

23 August 2020

copyright license

start time

24 August 2020

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April 2022 Public Data File from Crossref

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cites work

Structure-based design of antiviral drug candidates targeting the SARS-CoV-2 main protease

1 reference

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Structure of Mpro from COVID-19 virus and discovery of its inhibitors

10 February 2021

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Crystal structure of SARS-CoV-2 main protease provides a basis for design of improved α-ketoamide inhibitors

10 February 2021

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α-Ketoamides as Broad-Spectrum Inhibitors of Coronavirus and Enterovirus Replication: Structure-Based Design, Synthesis, and Activity Assessment

10 February 2021

1 reference

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Understanding Cell Penetration of Cyclic Peptides

10 February 2021

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Macrocyclic Peptides as Drug Candidates: Recent Progress and Remaining Challenges

10 February 2021

1 reference

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Cyclic Peptides: Promising Scaffolds for Biopharmaceuticals

10 February 2021

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Constrained peptides' time to shine?

10 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=7430054

SARS-CoV 3CL protease cleaves its C-terminal autoprocessing site by novel subsite cooperativity.

10 February 2021

1 reference

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Recent Progress in the Development of HIV-1 Protease Inhibitors for the Treatment of HIV/AIDS

10 February 2021

1 reference

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HIV protease inhibitors: a review of molecular selectivity and toxicity

10 February 2021

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HIV-1 antiretroviral drug therapy

10 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=7430054

In vitro selection of highly modified cyclic peptides that act as tight binding inhibitors

10 February 2021

1 reference

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AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading

10 February 2021

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UCSF Chimera--a visualization system for exploratory research and analysis

10 February 2021

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Adherence to protease inhibitor therapy and outcomes in patients with HIV infection

10 February 2021

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Inhibitors of HIV-1 protease: a major success of structure-assisted drug design

10 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=7430054

10 February 2021

HIV-protease inhibitors

1 reference

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Structure-based inhibitors of HIV-1 protease

10 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=7430054

10.26434/CHEMRXIV.12791954

10 February 2021

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32817929%20AND%20SRC:MED&resulttype=core&format=json

23 August 2020

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23 August 2020

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