A. Prahl

发表

Gold nanoparticles dispersion stability under dynamic coating conditions in capillary zone electrophoresis.

Krzesimir Ciura, B. Wielgomas, Szymon Dziomba, 2018, Journal of chromatography. A.

Studies of the Biological Properties of Human β-Defensin 1*

Jacek Lubkowski, D. Hoover, J. Lubkowski, 2007, Journal of Biological Chemistry.

Positional Scanning Identifies the Molecular Determinants of a High Affinity Multi-Leucine Inhibitor for Furin and PACE4.

R. Day, A. Kwiatkowska, A. Prahl, 2017, Journal of medicinal chemistry.

The Multi-Leu Peptide Inhibitor Discriminates Between PACE4 and Furin And Exhibits Antiproliferative Effects On Prostate Cancer Cells

R. Houghten, R. Day, M. Fugère, 2012, Journal of medicinal chemistry.

Interaction of Bradykinin and B2 Bradykinin Receptor Antagonists with Colloidal Au Surface Explored by Surface-Enhanced Raman Scattering

E. Proniewicz, A. Prahl, Dominika Skołuba, 2014 .

Influence of applied potential on bradykinin adsorption onto Ag, Au, and Cu electrodes

G. Niaura, E. Proniewicz, I. Ignatjev, 2013 .

Role of Phe‐D5 isotopically labeled analogues of bradykinin on elucidation of its adsorption mode on Ag, Au, and Cu electrodes. Surface‐enhanced Raman spectroscopy studies

G. Niaura, E. Proniewicz, I. Ignatjev, 2013 .

Improvement of derivatized amino acid detection sensitivity in micellar electrokinetic capillary chromatography by means of acid-induced pH-mediated stacking technique

T. Bączek, A. Bekasiewicz, P. Kowalski, 2014, Analytical and Bioanalytical Chemistry.

Design, Synthesis and Structure–Activity Relationship of New Arginine Vasopressin Analogues Containing Proline Derivatives in Position 2

M. Lewandowska, J. Slaninová, A. Kwiatkowska, 2013, Chemical biology & drug design.

Structure and conformation of Arg8 vasopressin modified analogs

L. Proniewicz, A. Prahl, E. Podstawka-Proniewicz, 2012 .

Novel analogues of arginine vasopressin containing α‐2‐indanylglycine enantiomers in position 2

J. Slaninová, A. Kwiatkowska, A. Prahl, 2010, Journal of peptide science : an official publication of the European Peptide Society.

Label-Free Electrochemical Test of Protease Interaction with a Peptide Substrate Modified Gold Electrode

A. Prahl, T. Ossowski, P. Niedziałkowski, 2021, Chemosensors.

Label-Free Electrochemical Test of Protease Interaction with a Peptide Substrate Modiﬁed Gold Electrode

A. Prahl, T. Ossowski, P. Niedziałkowski, 2021 .

Design and Structure-Activity Relationship of a Potent Furin Inhibitor Derived from Influenza Hemagglutinin.

R. Day, A. Kwiatkowska, A. Prahl, 2021, ACS medicinal chemistry letters.

Design, Synthesis, and Structure−Activity Relationship Studies of a Potent PACE4 Inhibitor

S. Beauchemin, R. Day, A. Kwiatkowska, 2014 .

Influence of enantiomers of 1-naphthylalanine in position 2 of VAVP and dVAVP on their pharmacological properties.

W. Kowalczyk, A. Prahl, H. Trzeciak, 2005, European journal of medicinal chemistry.

Is the Use of Surface-Enhanced Infrared Spectroscopy Justified in the Selection of Peptide Fragments That Play a Role in Substrate–Receptor Interactions? Adsorption of Amino Acids and Neurotransmitters on Colloidal Ag and Au Nanoparticles

E. Proniewicz, A. Prahl, E. Iłowska, 2021, The journal of physical chemistry. B.

B2 bradykinin receptor antagonists: adsorption mechanism on electrochemically roughened Ag substrate

A. Kudelski, E. Proniewicz, L. Proniewicz, 2013 .

Characterization of adsorption mode of new B2 bradykinin receptor antagonists onto colloidal Ag substrate

Y. Ozaki, E. Proniewicz, L. Proniewicz, 2013 .

Novel analogues of bradykinin conformationally restricted in the C‐terminal part of the molecule

J. Slaninová, A. Prahl, T. Wierzba, 2011, Journal of peptide science : an official publication of the European Peptide Society.

New bradykinin B(2) receptor antagonists - influence of C-terminal segment modifications on their pharmacological properties.

J. Zabrocki, J. Slaninová, A. Kwiatkowska, 2009, Acta biochimica Polonica.

New bradykinin analogues acylated on the N-terminus: effect on rat uterus and blood pressure.

J. Slaninová, A. Prahl, T. Wierzba, 2007, Acta biochimica Polonica.

New acylated bradykinin analogues: effect on rat blood pressure and rat uterus

W. Kowalczyk, J. Slaninová, A. Prahl, 2005, Journal of peptide science : an official publication of the European Peptide Society.

Potent bradykinin antagonists containing N-benzylglycine or N-benzyl-l-alanine in position 8.

W. Kowalczyk, J. Zabrocki, A. Prahl, 2008, The journal of peptide research : official journal of the American Peptide Society.

Novel Bradykinin Analogues Modified in the N-Terminal Part of the Molecule with a Variety of Acyl Substituents

J. Slaninová, A. Prahl, T. Wierzba, 2012, International Journal of Peptide Research and Therapeutics.

New bradykinin analogs in contraction of rat uterus,☆

A. Prahl, H. Trzeciak, B. Lammek, 2000, Peptides.

Lipidation of Temporin-1CEb Derivatives as a Tool for Activity Improvement, Pros and Cons of the Approach

A. Lesner, E. Sikorska, D. Wyrzykowski, 2021, International journal of molecular sciences.

Arginine-, d-arginine-vasopressin, and their inverso analogues in micellar and liposomic models of cell membrane: CD, NMR, and molecular dynamics studies

E. Sikorska, E. Lubecka, J. Slaninová, 2015, European Biophysics Journal.

Improving Fmoc Solid Phase Synthesis of Human Beta Defensin 3

G. Bulaj, A. Prahl, Aleksandra Walewska, 2022, International journal of molecular sciences.

Design, synthesis and biological activity of new neurohypophyseal hormones analogues conformationally restricted in the N-terminal part of the molecule. Highly potent OT receptor antagonists

J. Slaninová, A. Kwiatkowska, A. Prahl, 2011, Amino Acids.

Simultaneous determination of scopolamine, hyoscyamine and anisodamine in in vitro growth media of selected Solanaceae hairy roots by CE method.

P. Kowalski, Szymon Dziomba, A. Prahl, 2015, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Simultaneous Separation of Eight Benzodiazepines in Human Urine Using Field-Amplified Sample Stacking Micellar Electrokinetic Chromatography.

T. Bączek, A. Prahl, I. Olędzka, 2015, Journal of analytical toxicology.

Analogues of arginine vasopressin and its agonist and antagonist modified in the N-terminal part of the molecule with l-beta-homophenylalanine.

W. Kowalczyk, J. Zabrocki, J. Slaninová, 2005, The journal of peptide research : official journal of the American Peptide Society.

Reconstruction of the Conserved β-Bulge in Mammalian Defensins Using d-Amino Acids*

J. Lubkowski, Weiyue Lu, Wuyuan Lu, 2005, Journal of Biological Chemistry.

Studies on Sporopollenin Biosynthesis: The Effect of Inhibitors of Carotenoid Biosynthesis on Sporopollenin Accumulation

A. Prahl, R. Wiermann, K. Grumbach, 1985 .

Understanding the Role of Self-Assembly and Interaction with Biological Membranes of Short Cationic Lipopeptides in the Effective Design of New Antibiotics

Aleksandra Hać, E. Sikorska, W. Kamysz, 2022, Antibiotics.

Novel Bradykinin Analogues Modified in the N-Terminal Part of the Molecule with a Variety of Acyl Substituents

J. Slaninová, A. Prahl, T. Wierzba, 2012, International Journal of Peptide Research and Therapeutics.

Analogues of AVP modified in the N‐terminal part of the molecule with Pip isomers: TFA‐catalysed peptide bond hydrolysis

J. Slaninová, A. Kwiatkowska, A. Prahl, 2009, Journal of peptide science : an official publication of the European Peptide Society.

The effects of N-terminal part modification of arginine vasopressin analogues with 2-aminoindane-2-carboxylic acid: a highly potent V2 agonist.

W. Kowalczyk, J. Slaninová, A. Prahl, 2007, Journal of medicinal chemistry.

Analogues of neurohypophyseal hormones, oxytocin and arginine vasopressin, conformationally restricted in the N-terminal part of the molecule.

W. Kowalczyk, J. Zabrocki, J. Slaninová, 2006, Journal of medicinal chemistry.

New bradykinin analogues modified in the C-terminal part with sterically restricted 1-aminocyclohexane-1-carboxylic acid.

Tomasz H Wierzba, W. Kowalczyk, J. Slaninová, 2005, Journal of medicinal chemistry.

Highly potent 1-aminocyclohexane-1-carboxylic acid substituted V2 agonists of arginine vasopressin.

W. Kowalczyk, J. Slaninová, Wioleta Kowalczyk, 2004, Journal of medicinal chemistry.

Analogues of arginine vasopressin modified in the N-terminal part of the molecule with enantiomers of N-methylphenylalanine.

W. Kowalczyk, J. Slaninová, A. Prahl, 2004, The journal of peptide research : official journal of the American Peptide Society.

Arginine vasopressin and its analogues--the influence of position 2 modification with 3,3-diphenylalanine enantiomers. Highly potent V2 agonists.

J. Slaninová, A. Kwiatkowska, A. Prahl, 2009, European journal of medicinal chemistry.

Analogues of arginine vasopressin modified at position 2 with proline derivatives: selective antagonists of oxytocin in vitro.

J. Slaninová, A. Prahl, B. Lammek, 2009, Advances in Experimental Medicine and Biology.

Adsorption of (Phe-h5)/(Phe-d5)-substituted peptides from neurotensin family on the nanostructured surfaces of Ag and Cu: SERS studies.

A. Kudelski, E. Proniewicz, A. Prahl, 2020, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

Highly Potent Antidiuretic Antagonists: Conformational Studies of Vasopressin Analogues Modified with 1‐Naphthylalanine Enantiomers at Position 2

E. Sikorska, E. Lubecka, A. Prahl, 2012, Chemical biology & drug design.

The influence of 1‐aminocyclopentane‐1‐carboxylic acid at position 2 or 3 of AVP and its analogues on their pharmacological properties

W. Kowalczyk, J. Slaninová, A. Prahl, 2005, Journal of peptide science : an official publication of the European Peptide Society.

Structure of the isoaspartyl peptidase with L-asparaginase activity from Escherichia coli.

W. Lockau, J. Lubkowski, Mahdi Hejazi, 2004, Acta Crystallographica Section D: Biological Crystallography.

Structure of human monocyte chemoattractant protein 4 (MCP-4/CCL13).

J. Lubkowski, C. Bařinka, A. Prahl, 2008, Acta crystallographica. Section D, Biological crystallography.

Potent antidiuretic agonists, deamino‐vasopressin and desmopressin, and their inverso analogs: NMR structure and interactions with micellar and liposomic models of cell membrane

E. Sikorska, E. Lubecka, J. Slaninová, 2016, Biopolymers.

Macrocyclization of a potent PACE4 inhibitor: Benefits and limitations.

R. Day, A. Kwiatkowska, A. Prahl, 2017, European journal of cell biology.

nfluence of photoinitiator type on the rate of olymerization , degree of conversion , hardness nd yellowing of dental resin composites uis

A. Prahl, F. Schneidera, C. Pfeiferb, 2008 .

New Aspects of Sporopollenin Biosynthesis

A. Prahl, R. Wiermann, M. Rittscher, 1986 .

Influence of conformationally constrained amino acids replacing positions 2 and 3 of arginine vasopressin (AVP) and its analogues on their pharmacological properties.

J. Slaninová, A. Kwiatkowska, A. Prahl, 2007, Protein and peptide letters.

Bradykinin and Neurotensin Analogues as Potential Compounds in Colon Cancer Therapy

A. Prahl, E. Iłowska, A. Olejniczak-Kęder, 2023, International journal of molecular sciences.

Spectroscopic characterization and in vitro studies of biological activity of bradykinin derivatives

E. Proniewicz, A. Prahl, G. Burnat, 2022, Scientific Reports.

New bradykinin analogues substituted in positions 7 and 8 with sterically restricted 1‐aminocyclopentane‐1‐carboxylic acid

W. Kowalczyk, J. Slaninová, A. Prahl, 2006, Journal of Peptide Science.

Bradykinin analogues acylated on their N-terminus--some recent development.

A. Prahl, D. Sobolewski, 2009, Advances in experimental medicine and biology.

Application of Alanine Scanning to Determination of Amino Acids Essential for Peptide Adsorption at the Solid/Solution Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared Spectroscopy versus Bioactivity Assays

E. Proniewicz, A. Prahl, M. Makowska, 2021, Journal of medicinal chemistry.

Tip-enhanced Raman spectroscopy of bradykinin and its B 2 receptor antagonists onto colloidal suspended Ag nanowires

Y. Ozaki, S. Vantasin, E. Proniewicz, 2015 .

Modifications in the bradykinin main chain are not necessary for antagonistic activity in rat blood pressure assay

A. Prahl, 2007, Journal of peptide science : an official publication of the European Peptide Society.

Desing and synhesis of new bradykinin antagonist with N-terminal acylation.

A. Prahl, T. Wierzba, B. Lammek, 1997 .

Antagonists of Bradykinin Modified with Conformationally Restricted Dipeptide Fragment.

P. Winklewski, A. Prahl, T. Wierzba, 1997 .

New analogues of bradykinin containing a conformationally restricted dipeptide fragment in their molecules.

A. Prahl, H. Trzeciak, K. Neubert, 2001, The journal of peptide research : official journal of the American Peptide Society.

INFLUENCE OF C-TERMINAL MODIFICATIONS OF BRADYKININ ANTAGONISTS ON THEIR ACTIVITY

P. Winklewski, A. Prahl, T. Wierzba, 1997 .

From pro defensins to defensins: synthesis and characterization of human neutrophil pro alpha-defensin-1 and its mature domain.

J. Lubkowski, A. Prahl, Bryan Ericksen, 2003, The journal of peptide research : official journal of the American Peptide Society.

Tip-enhanced Raman spectroscopy of bradykinin and its B2 receptor antagonists adsorbed onto colloidal suspended Ag nanowires.

Y. Ozaki, S. Vantasin, E. Proniewicz, 2015, Physical chemistry chemical physics : PCCP.

Lipidation of Naturally Occurring α-Helical Antimicrobial Peptides as a Promising Strategy for Drug Design

E. Sikorska, D. Wyrzykowski, A. Prahl, 2023, International journal of molecular sciences.

Evaluation of sample injection precision in respect to sensitivity in capillary electrophoresis using various injection modes.

M. Markuszewski, Krzesimir Ciura, J. Nowakowska, 2017, Journal of separation science.

Human β-defensin 4 - defensin without the "twist".

J. Lubkowski, M. Pazgier, J. Alexandratos, 2016, Postepy biochemii.

Analogs of arginine vasopressin modified in the N‐terminal part of the molecule with a conformationally constrained cis‐peptide bond motif

K. Kaczmarek, J. Zabrocki, J. Slaninová, 2007, Journal of peptide science : an official publication of the European Peptide Society.

Analogues of arginine vasopressin modified in position 2 and 3 with conformationally constrained dipeptide fragments

W. Kowalczyk, Elżbieta Łempicka, A. Prahl, 2005, Journal of peptide science : an official publication of the European Peptide Society.

Design, Synthesis, and Structure−Activity Relationship Studies of a Potent PACE4 Inhibitor

S. Beauchemin, R. Day, A. Kwiatkowska, 2014 .

[Proprotein convertases - family of serine proteases with a broad spectrum of physiological functions].

E. Sikorska, A. Prahl, Aleksandra Walewska, 2016, Postepy biochemii.