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Chemical structure and properties of low-molecular furin inhibitors

Ukrainian biochemical journal, 2016-11, Vol.88 (6), p.5-25

2016

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Synthesis, biological evaluation and docking of novel bisamidinohydrazones as non-peptide inhibitors of furin

Ukrainian biochemical journal, 2015, Vol.87 (1), p.55-63

2015

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Influence of organic solvents on the furin activity

Ukrainian biochemical journal, 2018-10, Vol.90 (5), p.28-33

2018

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Synthesis and investigation of the derivatives of amidinohydrazonelated aromatic compounds as furin inhibitors

Ukrainian biochemical journal, 2017-12, Vol.89 (6), p.3-12

2017

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Influence of cations on furin activity

Ukrainian biochemical journal, 2017-10, Vol.89 (5), p.15-20

2017

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FURIN INHIBITORS BASED ON THE DERIVATIVES OF CALIX[4]ARENE CX3im

Ukrainian biochemical journal, 2015-05, Vol.87 (3), p.31-36

2015

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Non-peptide furin inhibitors based on amidinohydrazones of diarylaldehydes

Ukrainian biochemical journal, 2013-02, Vol.85 (1), p.22-32

2013

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References. Mechanisms of biochemical reactions: a textbook edited by Professor N.O. Sibirna. Second Edition, supplemented. Lviv: Ivan Franko LNU.2011. – 320 p. – Series "Biological Studies"

Bìologìčnì studìï, 2012, Vol.6 (3), p.255-235

Kibirev, V. K.

2012

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1,3-Oxazol-4-ylphosphonium salts as new non-peptide inhibitors of furin

Ukrainian biochemical journal, 2019-08, Vol.91 (4), p.5-16

2019

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Synthesis and Study on a Novel Inhibitor of Thrombin Containing No Side Chain at the P1 Position of the Polypeptide Chain

Seminars in thrombosis and hemostasis, 1996, Vol.22 (4), p.343-345

1996

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The synthesis of arginine derivatives of chromone and azauracil

Russian journal of bioorganic chemistry, 2006-05, Vol.32 (3), p.277-279

2006

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The synthesis of arginine derivatives of chromone and azauracil

Bioorganicheskaia khimiia, 2006-05, Vol.32 (3), p.308

2006

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New donor-acceptor pairs for fluorogenic substrates with intramolecular fluorescence energy transfer for thrombin and trypsin

Bioorganicheskaia khimiia, 1998-03, Vol.24 (3), p.179

1998

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Structure and properties of proprotein convertase inhibitors

Ukrains'kyi biokhimichnyi zhurnal (1999 ), 2012-03, Vol.84 (2), p.5

2012

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Synthesis and antithrombin activity of phosphoalanine-containing peptides

Bioorganicheskaia khimiia, 2003-05, Vol.29 (3), p.247

2003

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Solid-state conjugation of proteins with hydrophobic compounds in non-denaturing conditions: I. Acylation of proteins by dansyl proline using a polymeric N-hydroxysuccinimide ester

Journal of biochemical and biophysical methods, 2000-09, Vol.45 (2), p.183-191

2000

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Non-peptide furin inhibitors based on amidinohydrazones of diarylaldehydes

Ukrains'kyi biokhimichnyi zhurnal (1999 ), 2013-01, Vol.85 (1), p.22

2013

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Furin and its biological role

Ukrains'kyi biokhimichnyi zhurnal (1999 ), 2007-11, Vol.79 (6), p.5

2007

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New non-peptide inhibitors of furin

Ukrains'kyi biokhimichnyi zhurnal (1999 ), 2010-03, Vol.82 (2), p.15

2010

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Affinity chromatography of human gamma-thrombin on fibrin-agarose

Ukrainskij biohimičeskij žurnal, 1988-07, Vol.60 (4), p.24

1988

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Similarity of the effects of tosyl-L-arginine methyl ester, atropine, caffeine and antitumour alkylating agent on some biological functions of thrombin and platelet 12-lipoxygenase

Ukrainskij biohimičeskij žurnal, 1993-09, Vol.65 (5), p.37

1993

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Study on derivatives of 5-amino-4-acylamino-1H-pyrazole as inhibitors of furin

Ukrains'kyi biokhimichnyi zhurnal (1999 ), 2011-01, Vol.83 (1), p.30

2011

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Study on secondary structure and properties of alpha- and gamma-forms of human thrombin

Ukrains'kyi biokhimichnyi zhurnal (1999 ), 2006-01, Vol.78 (1), p.87

2006

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Chromogenic and fluorogenic peptide substrates of proteolytic enzymes

Bioorganicheskaia khimiia, 1988-11, Vol.14 (11), p.1461

1988

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Natural and synthetic inhibitors of thrombin. II. Synthetic low-molecular-weight inhibitors

Ukrains'kyi biokhimichnyi zhurnal (1999 ), 1999-01, Vol.71 (1), p.16

1999

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Chemical structure and properties of low-molecular furin inhibitors

Synthesis, biological evaluation and docking of novel bisamidinohydrazones as non-peptide inhibitors of furin

Influence of organic solvents on the furin activity

Synthesis and investigation of the derivatives of amidinohydrazonelated aromatic compounds as furin inhibitors

Influence of cations on furin activity

FURIN INHIBITORS BASED ON THE DERIVATIVES OF CALIX[4]ARENE CX3im

Non-peptide furin inhibitors based on amidinohydrazones of diarylaldehydes

References. Mechanisms of biochemical reactions: a textbook edited by Professor N.O. Sibirna. Second Edition, supplemented. Lviv: Ivan Franko LNU.2011. – 320 p. – Series "Biological Studies"

1,3-Oxazol-4-ylphosphonium salts as new non-peptide inhibitors of furin

Synthesis and Study on a Novel Inhibitor of Thrombin Containing No Side Chain at the P1 Position of the Polypeptide Chain

The synthesis of arginine derivatives of chromone and azauracil

The synthesis of arginine derivatives of chromone and azauracil

New donor-acceptor pairs for fluorogenic substrates with intramolecular fluorescence energy transfer for thrombin and trypsin

Structure and properties of proprotein convertase inhibitors

Synthesis and antithrombin activity of phosphoalanine-containing peptides

Solid-state conjugation of proteins with hydrophobic compounds in non-denaturing conditions: I. Acylation of proteins by dansyl proline using a polymeric N-hydroxysuccinimide ester

Non-peptide furin inhibitors based on amidinohydrazones of diarylaldehydes

Furin and its biological role

New non-peptide inhibitors of furin

Affinity chromatography of human gamma-thrombin on fibrin-agarose

Similarity of the effects of tosyl-L-arginine methyl ester, atropine, caffeine and antitumour alkylating agent on some biological functions of thrombin and platelet 12-lipoxygenase

Study on derivatives of 5-amino-4-acylamino-1H-pyrazole as inhibitors of furin

Study on secondary structure and properties of alpha- and gamma-forms of human thrombin

Chromogenic and fluorogenic peptide substrates of proteolytic enzymes

Natural and synthetic inhibitors of thrombin. II. Synthetic low-molecular-weight inhibitors

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