Peptide-derived transition state analogue inhibitors of thrombin; Synthesis, activity and selectivity (Q71797846)

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21 October 2019

title

Peptide-derived transition state analogue inhibitors of thrombin; synthesis, activity and selectivity (English)

1 reference

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21 October 2019

Peptide-derived transition state analogue inhibitors of thrombin; Synthesis, activity and selectivity (English)

1 reference

https://api.crossref.org/works/10.1016/0968-0896(95)00102-M

23 May 2024

author name string

M. Jetten

1

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23 May 2024

C. A. Peters

2

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23 May 2024

A. Visser

3

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23 May 2024

P. D. Grootenhuis

4

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23 May 2024

J. W. van Nispen

5

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23 May 2024

H. C. Ottenheijm

6

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language of work or name

English

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publication date

1 August 1995

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full work available at URL

21 October 2019

https://api.elsevier.com/content/article/PII:096808969500102M?httpAccept=text/xml

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https://api.elsevier.com/content/article/PII:096808969500102M?httpAccept=text/plain

23 May 2024

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Bioorganic & Medicinal Chemistry

23 May 2024

published in

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21 October 2019

volume

3

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21 October 2019

issue

8

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21 October 2019

page(s)

1099-1114

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21 October 2019

2

25

597

Wallis

1989

1 reference

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Synthesis and biological activity of ketomethylene pseudopeptide analogues as thrombin inhibitors

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8

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A new series of synthetic thrombin-inhibitors (OM-inhibitors) having extremely potent and selective action

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11

1 reference

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Potent inhibition of thrombin by the newly synthesized arginine derivative No. 805. The importance of stereo-structure of its hydrophobic carboxamide portion

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12

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D-PHE-PRO-ARGCH2Cl-A selective affinity label for thrombin

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Highly active and selective anticoagulants: D-Phe-Pro-Arg-H, a free tripeptide aldehyde prone to spontaneous inactivation, and its stable N-methyl derivative, D-MePhe-Pro-Arg-H

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16

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Cyclic amides of N alpha-arylsulfonylaminoacylated 4-amidinophenylalanine--tight binding inhibitors of thrombin

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Molecular Architecture and Biological Reactions

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18

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Transition State Analogues for Enzyme Catalysis

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20

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The interaction of thrombin with fibrinogen. A structural basis for its specificity

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22

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On the size of the active site in proteases. I. Papain

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23

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Journal of Biological Chemistry

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24

260

14

1985

1 reference

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

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Study of the Specificity of Thrombin with Tripeptidyl-p-nitroanilide Substrates

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A new class of potent thrombin inhibitors that incorporates a scissile pseudopeptide bond

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Synthesis of arphamenine A and epi-arphamenine A

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A new synthesis of N alpha,NG,G-tribenzyloxycarbonyl-L-arginine and related derivatives

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High-performance liquid chromatographic determination of enantiomeric amino acids and amino alcohols after derivatization with o-phthaldialdehyde and various chiral mercaptans. Application to peptide hydrolysates

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Converting trypsin to chymotrypsin: the role of surface loops

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Identifiers

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21 October 2019

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