(Q31440216)

2 July 2017

title

New bivalent thrombin inhibitors with N(alpha)(methyl)arginine at the P1-position (English)

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2 July 2017

8

Stürzebecher J

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2 July 2017

Steinmetzer T

1

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2 July 2017

Batdordshjin M

2

1 reference

2 July 2017

Pineda F

3

1 reference

2 July 2017

Seyfarth L

4

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2 July 2017

Vogel A

5

1 reference

2 July 2017

Reissmann S

6

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2 July 2017

Hauptmann J

7

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2 July 2017

language of work or name

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1 July 2000

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2 July 2017

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2 July 2017

volume

381

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2 July 2017

issue

7

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2 July 2017

page(s)

603-610

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The refined 1.9-Å X-ray crystal structure of d-Phe-Pro-Arg chloromethylketone-inhibited human α-thrombin: Structure analysis, overall structure, electrostatic properties, detailed active-site geometry, and structure-function relationships

2 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Use of site-directed mutagenesis to investigate the basis for the specificity of hirudin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Proline specific peptidases

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Synthesis of a homologous series of ketomethylene arginyl pseudodipeptides and application to low molecular weight hirudin-like thrombin inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Synthetic inhibitors of thrombin and factor Xa: from bench to bedside

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Designing peptide and protein ligands for biological receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Hirulog peptides with scissile bond replacements resistant to thrombin cleavage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Synthesis, structure, and structure-activity relationships of divalent thrombin inhibitors containing an alpha-keto-amide transition-state mimetic

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Probing intermolecular main chain hydrogen bonding in serine proteinase-protein inhibitor complexes: chemical synthesis of backbone-engineered turkey ovomucoid third domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Structure of the hirulog 3-thrombin complex and nature of the S' subsites of substrates and inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Crystal structure of a peptidyl pyridinium methyl ketone inhibitor with thrombin

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

The structure of a complex of recombinant hirudin and human alpha-thrombin

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Design and evaluation of novel bivalent thrombin inhibitors based on amidinophenylalanines

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Kinetics of the inhibition of thrombin by hirudin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

A player of many parts: the spotlight falls on thrombin's structure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

Design of potent bivalent thrombin inhibitors based on hirudin sequence: incorporation of nonsubstrate-type active site inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

LIGPLOT: a program to generate schematic diagrams of protein-ligand interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2000.077

21 January 2018

Identifiers

DOI

10.1515/BC.2000.077

1 reference

2 July 2017

1 reference