An efficient method for the synthesis of peptide aldehyde libraries employed in the discovery of reversible SARS coronavirus main protease (SARS-CoV Mpro) inhibitors (Q33243091)

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English	An efficient method for the synthesis of peptide aldehyde libraries employed in the discovery of reversible SARS coronavirus main protease (SARS-CoV Mpro) inhibitors	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

24 July 2017

An efficient method for the synthesis of peptide aldehyde libraries employed in the discovery of reversible SARS coronavirus main protease (SARS-CoV Mpro) inhibitors (English)

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Europe PubMed Central

PubMed publication ID

24 July 2017

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1 reference

based on heuristic

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Samer I Al-Gharabli

object named as

Samer I Al-Gharabli

1

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object named as

Jörg Rademann

9

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Rolf Hilgenfeld

8

object named as

Rolf Hilgenfeld

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Europe PubMed Central

PubMed publication ID

24 July 2017

author name string

Syed T Ali Shah

2

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Europe PubMed Central

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24 July 2017

Steffen Weik

3

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Europe PubMed Central

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24 July 2017

Marco F Schmidt

4

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Europe PubMed Central

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24 July 2017

Jeroen R Mesters

5

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Europe PubMed Central

PubMed publication ID

24 July 2017

Daniel Kuhn

6

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24 July 2017

Gerhard Klebe

7

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24 July 2017

publication date

1 July 2006

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24 July 2017

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Europe PubMed Central

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24 July 2017

7

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24 July 2017

7

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24 July 2017

1048-1055

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24 July 2017

Conservation medicine and a new agenda for emerging diseases

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Molecular mechanisms of severe acute respiratory syndrome (SARS)

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Aetiology: Koch's postulates fulfilled for SARS virus

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Gene therapy progress and prospects: novel gene therapy approaches for AIDS.

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Insertions in the human immunodeficiency virus type 1 protease and reverse transcriptase genes: clinical impact and molecular mechanisms

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The crystal structures of severe acute respiratory syndrome virus main protease and its complex with an inhibitor

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Coronavirus main proteinase (3CLpro) structure: basis for design of anti-SARS drugs

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

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Peptide aldehydes as inhibitors of HIV protease.

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A novel heterodimeric cysteine protease is required for interleukin-1 beta processing in monocytes

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Preparations of psi-peptide bond and peptide-aldehyde inhibitors of atrial granule serine proteinase, a candidate processing enzyme of pro-atrial natriuretic factor

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21 January 2018

A simple method for semi-synthesis of peptidyl-argininals as potent inhibitors of trypsin-like proteases

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Oxidizing Polymers: A Polymer-Supported, Recyclable Hypervalent Iodine(V) Reagent for the Efficient Conversion of Alcohols, Carbonyl Compounds, and Unsaturated Carbamates in Solution J.R. gratefully acknowledges generous support from Prof. M. E. Mai

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

A new method to detect related function among proteins independent of sequence and fold homology.

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21 January 2018

A fast flexible docking method using an incremental construction algorithm.

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Progress in the preparation of peptide aldehydes via polymer supported IBX oxidation and scavenging by threonyl resin

1 reference

https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

pH-dependent conformational flexibility of the SARS-CoV main proteinase (M(pro)) dimer: molecular dynamics simulations and multiple X-ray structure analyses

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Design of wide-spectrum inhibitors targeting coronavirus main proteases

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Crystal structures of the main peptidase from the SARS coronavirus inhibited by a substrate-like aza-peptide epoxide.

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Solid-phase synthesis of oligourea peptidomimetics employing the Fmoc protection strategy.

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Backbone amide linker (BAL) strategy for Nalpha-9-fluorenylmethoxycarbonyl (Fmoc) solid-phase synthesis of peptide aldehydes

1 reference

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21 January 2018

Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides

1 reference

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21 January 2018

Improved solid phase synthesis of C-terminal peptide aldehydes

1 reference

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21 January 2018

Aldehydic peptides inhibiting renin

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Preparation and evaluation of peptidic aspartyl hemiacetals as reversible inhibitors of interleukin-1 beta converting enzyme (ICE)

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21 January 2018

Inhibition studies of some serine and thiol proteinases by new leupeptin analogues

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21 January 2018

Screening for fibrinolysis inhibitory effect of synthetic thrombin inhibitors

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https://api.crossref.org/works/10.1002%2FCBIC.200500533

21 January 2018

Synthesis of lipopeptides using hydrazone chemical ligation

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https://pubmed.ncbi.nlm.nih.gov/16688706

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SARS risk perceptions in healthcare workers, Japan

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[Severe acute respiratory syndrome. The public health laboratory in a global emergency].

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12 December 2020

based on heuristic

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Identifiers

10.1002/CBIC.200500533

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

PMC publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

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