J. Slaninová

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Effect of hydrocarbon stapling on the properties of α-helical antimicrobial peptides isolated from the venom of hymenoptera

V. Čeřovský, L. Bednárová, Hubert Chapuis, 2012, Amino Acids.

The influence of steric interactions on the conformation and biology of oxytocin. Synthesis and analysis of penicillamine(6)-oxytocin and penicillamine(6)-5-tert-butylproline(7)-oxytocin analogs.

L. Bélec, W. Lubell, J. Slaninová, 2001, The journal of peptide research : official journal of the American Peptide Society.

Pseudoprolines for Studying Bioactive cis -Prolyl Conformations

M. Mutter, J. Slaninová, L. Patiny, 2001 .

Structure–activity study of macropin, a novel antimicrobial peptide from the venom of solitary bee Macropis fulvipes (Hymenoptera: Melittidae)

V. Veverka, V. Čeřovský, L. Bednárová, 2014, Journal of peptide science : an official publication of the European Peptide Society.

Structure-activity studies of a novel bicyclic oxytocin antagonist.

V. Hruby, D. Smith, J. Slaninová, 1992, Journal of medicinal 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.

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.

Synthesis and biological activity of oxytocin analogues containing unnatural amino acids in position 9: structure activity study

P. Cordopatis, J. Slaninová, V. Magafa, 2010, Amino Acids.

Oxytocin analogues with amide groups substituted by tetrazole groups in position 4, 5 or 9.

J. Slaninová, Z. Grzonka, Lenka Borovičková, 2007, Acta biochimica Polonica.

Synthesis and biological evaluation of oxytocin analogues containing l-α-t-butylglycine [Gly(Bu t )] in positions 8 or 9

P. Cordopatis, M. Fragiadaki, J. Slaninová, 2003, Peptides.

Effect of cholecystokinin on feeding is attenuated in monosodium glutamate obese mice

A. Kiss, M. Haluzík, J. Slaninová, 2006, Regulatory Peptides.

Cholecystokinin Analogs with Suppressed Central Activities

J. Slaninová, L. Maletínská, J. Hlaváček, 1998, Peptides.

Pharmacological characterization of new cholecystokinin analogues.

M. Galas, J. Slaninová, L. Maletínská, 1992, European journal of pharmacology.

In vitro binding and in vivo biodistribution studies of the neuroprotective peptide humanin using [125I]humanin derivatives

D. Benaki, J. Slaninová, P. Bouziotis, 2009, Peptides.

Melectin MAPs: the influence of dendrimerization on antimicrobial and hemolytic activity

J. Ježek, V. Čeřovský, L. Bednárová, 2010, Amino Acids.

Functional characterization of two defensin isoforms of the hard tick Ixodes ricinus

D. Růžek, N. Rudenko, L. Grubhoffer, 2011, Parasites & Vectors.

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.

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.

The Dose-Dependent Effects of Multifunctional Enkephalin Analogs on the Protein Composition of Rat Spleen Lymphocytes, Cortex, and Hippocampus; Comparison with Changes Induced by Morphine

P. Svoboda, J. Slaninová, Y. Lee, 2022, Biomedicines.

The antifungal effect of peptides from hymenoptera venom and their analogs

V. Čeřovský, J. Slaninová, L. Monincová, 2011, Central European Journal of Biology.

Interaction of a novel antimicrobial peptide isolated from the venom of solitary bee Colletes daviesanus with phospholipid vesicles and Escherichia coli cells

V. Čeřovský, L. Bednárová, J. Slaninová, 2014, Journal of peptide science : an official publication of the European Peptide Society.

Synthesis of lucifensin by native chemical ligation and characteristics of its isomer having different disulfide bridge pattern

V. Čeřovský, L. Bednárová, J. Slaninová, 2014, Journal of peptide science : an official publication of the European Peptide Society.

Lucifensin, a Novel Insect Defensin of Medicinal Maggots: Synthesis and Structural Study

V. Čeřovský, L. Bednárová, J. Slaninová, 2011, Chembiochem : a European journal of chemical biology.

Cocaine- and amphetamine-regulated transcript (CART) peptide specific binding in pheochromocytoma cells PC12.

E. Šloncová, J. Slaninová, B. Železná, 2007, European journal of pharmacology.

In position 7 l- and d-Tic-substituted oxytocin and deamino oxytocin: NMR study and conformational insights

G. Spyroulias, P. Cordopatis, M. Fragiadaki, 2010, Amino Acids.

Designing peptidomimetic antagonists for peptide receptors: topochemical differences of agonists and antagonists

V. Hruby, H. Yamamura, F. Porreca, 1999 .

Insect oostatic peptide: absence of effect on mice ovaries.

J. Slaninová, R. Tykva, B. Bennettová, 2002, Chemosphere.

Oostatic peptides containing d-amino acids: synthesis, oostatic activity, degradation, accumulation in ovaries and NMR study

J. Slaninová, M. Buděšínský, R. Tykva, 2012, Amino Acids.

1-Deamino-1(15)-carba and -Dicarba Analogues of Endothelin-1

J. Slaninová, M. Buděšínský, J. Hlaváček, 2000 .

Rational design, efficient syntheses and biological evaluation of N,N'-symmetrically bis-substituted butylimidazole analogs as a new class of potent Angiotensin II receptor blockers.

G. Melagraki, A. Afantitis, G. Liapakis, 2013, European journal of medicinal chemistry.

Novel biologically active peptides from the venom of the solitary bee Macropis fulvipes (hymenoptera: melittidae)

Z. Voburka, V. Čeřovský, L. Bednárová, 2009 .

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.

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.

Analogs of oxytocin conformationally restricted in the N-terminal part of the molecule.

J. Slaninová, B. Lammek, I. Derdowska, 2001, The journal of peptide research : official journal of the American Peptide Society.

Panurgines, novel antimicrobial peptides from the venom of communal bee Panurgus calcaratus (Hymenoptera: Andrenidae)

Z. Voburka, V. Čeřovský, L. Bednárová, 2013, Amino Acids.

Lasiocepsin, a novel cyclic antimicrobial peptide from the venom of eusocial bee Lasioglossum laticeps (Hymenoptera: Halictidae)

Z. Voburka, V. Čeřovský, L. Bednárová, 2012, Amino Acids.

Cyclic enkephalin analogs that are hybrids of DPDPE-related peptides and metenkephalin-Arg-Gly-Leu: prohormone analogs that retain good potency and selectivity for delta opioid receptors.

V. Hruby, H. Yamamura, F. Porreca, 1999, The journal of peptide research : official journal of the American Peptide Society.

Radiochromatographic assay of metabolites of the oostatic peptide labeled in different positions of the peptide chain.

J. Slaninová, R. Tykva, B. Černý, 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Non‐sequential vasopressin peptides. Stereochemistry and biological activity

A. Machová, M. Zaoral, J. Slaninová, 2000, Journal of peptide science : an official publication of the European Peptide Society.

Cholecystokinin analogues with alkylated carboxy terminal phenylalanine

J. Slaninová, P. Majer, L. Maletínská, 1991 .

Solid phase synthesis and biological activities of [Arg8]-vasopressin methylenedithioether.

M. Ueki, M. Williamson, T. Asakura, 1999, Bioorganic & medicinal chemistry letters.

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.

Direct evidence for an angiotensin AT1 receptor type in rat vas deferens.

J. Slaninová, B. Železná, J. Kuneš, 1998, European journal of pharmacology.

Oostatic peptides containing d-amino acids: synthesis, oostatic activity, degradation, accumulation in ovaries and NMR study

J. Slaninová, M. Buděšínský, R. Tykva, 2012, Amino Acids.

Study of Oostatic Peptide Uptake and Metabolism in Developing Ovaries of the Flesh Fly, Neobellieria bullata

J. Slaninová, R. Tykva, J. Holík, 2010, Journal of insect science.

Metabolic cleavage of N- and C-terminal amino acids of an insect oostatic peptide H-Tyr-Asp-Pro-Ala-Pro-OH

J. Slaninová, R. Tykva, B. Černý, 2005 .

Activity and mechanism of action of insect oostatic peptides in flesh fly.

P. Šimek, J. Slaninová, R. Tykva, 2004, Bioorganic chemistry.

Opioid receptor binding properties of analgesic analogues of cholecystokinin octapeptide.

V. Hruby, T. Burks, R. Knapp, 1991, European journal of pharmacology.

Antinociceptive profile of biphalin, a dimeric enkephalin analog.

S. Appleyard, A. Misicka, H. Yamamura, 1993, The Journal of pharmacology and experimental therapeutics.

Cyclic enkephalin analogs with exceptional potency at peripheral delta opioid receptors.

V. Hruby, H. Yamamura, T. Zalewska, 1994, Journal of medicinal chemistry.

[125I-Tyr1]biphalin binding to opioid receptors of rat brain and NG108-15 cell membranes.

S. Appleyard, V. Hruby, R. Knapp, 1998, Life sciences.

Cyclic enkephalin analogues with exceptional potency and selectivity for δ-opioid receptors

V. Hruby, H. Yamamura, T. Zalewska, 1997 .

Cyclic enkephalin analogues with exceptional potency and selectivity for delta-opioid receptors.

V. Hruby, H. Yamamura, T. Zalewska, 1997, Journal of medicinal chemistry.

Analogues of cholecystokinin 26–33 selective for B-type CCK receptors possess δ opioid receptor agonist activity in vitro and in vivo: Evidence for similarities in CCK-B and δ opioid receptor requirements

V. Hruby, G. Nikiforovich, T. Burks, 1994 .

[125I]SNF 8702: A selective radioligand for CCKB receptors

V. Hruby, R. Knapp, H. Yamamura, 1995, Peptides.

Neuroprotective peptides as drug candidates against Alzheimer's diasease

J. Patočka, J. Slaninová, G. Kunešová, 2005 .

Bioportide: an emergent concept of bioactive cell-penetrating peptides

C. Östenson, J. McKeating, Ü. Langel, 2012, Cellular and Molecular Life Sciences.

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.

Depletion of calcium stores contributes to progesterone-induced attenuation of calcium signaling of G protein-coupled receptors

G. Gimpl, Katja Gehrig-Burger, J. Slaninová, 2010, Cellular and Molecular Life Sciences.

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.

Influence of 1-aminocyclohexane-1-carboxylic acid in position 2 or 3 of AVP and its analogues on their pharmacological properties.

W. Kowalczyk, B. Jastrzebska, A. Machová, 2003, The journal of peptide research : official journal of the American Peptide Society.

The multiple T-maze in vivo testing of the neuroprotective effect of humanin analogues

D. Benaki, J. Patočka, J. Slaninová, 2008, Peptides.

Effect of humanin analogues on experimentally induced impairment of spatial memory in rats

J. Patočka, J. Slaninová, G. Krejčová, 2004, Journal of peptide science : an official publication of the European Peptide Society.

Novel strategies for the design of receptor‐selective vasopressin analogues: Aib‐substitution and retro‐inverso transformation

J. Howl, M. Wheatley, J. Slaninová, 1999, British journal of pharmacology.

Synthesis and biological activity of oxytocin analogues containing conformationally-restricted residues in position 7.

P. Cordopatis, M. Fragiadaki, J. Slaninová, 2007, European journal of medicinal chemistry.

The analogs of oxytocin and D-homoarginine vasopressin with bulky substituted phenylalanine in position 2

J. Slaninová, Z. Procházka, M. Žertová, 2000, Letters in Peptide Science.

Structural studies with weak oxytocin antagonists

N. Assimomytis, P. Cordopatis, J. Slaninová, 1996, Letters in Peptide Science.

Activity of the Parallel Dimer of Jl)eamino-Oxytocin

J. Slaninová, M. Munson, 1993 .

Novel antimicrobial peptides from the venom of the eusocial bee Halictus sexcinctus (Hymenoptera: Halictidae) and their analogs

Z. Voburka, J. Cvačka, V. Čeřovský, 2010, Amino Acids.

Lasioglossins: Three Novel Antimicrobial Peptides from the Venom of the Eusocial Bee Lasioglossum laticeps (Hymenoptera: Halictidae)

Z. Voburka, J. Cvačka, V. Čeřovský, 2009, Chembiochem : a European journal of chemical biology.

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.

THE DEAMINO-CARBA ANALOGS OF VASOTOCIN. SYNTHESIS AND SOME BIOLOGICAL PROPERTIES*

M. Lebl, J. Slaninová, P. Melin, 1994 .

Analogs of Deamino Carba Oxytocin with Inhibitory Properties; Synthesis and Biological Activities

M. Lebl, T. Barth, J. Slaninová, 1992 .

Amino and Deamino Analogs of 8-D-Homoarginin-vasopressin with Modified Tyrosine in Position 2: Synthesis and Some Biological Properties

M. Lebl, T. Barth, J. Slaninová, 1992 .

Oxytocin analogues with non-coded amino acid residues in position 8: [8-Neopentylglycine]oxytocin and [8-cycloleucine]oxytocin

V. Hruby, J. Slaninová, J. Hlaváček, 1987 .

The deamino carba analogs of [Phe2, Orn8]vasotocin

M. Lebl, J. Slaninová, P. Melin, 1993 .

Amino Acids and Peptides. Part 202. Oxytocin Analogues with Non-Coded Amino Acid Residues in Position 8: (8-Neopentylglycine)oxytocin and (8-Cycloleucine)oxytocin.

V. Hruby, J. Slaninová, J. Hlaváček, 1988 .

Design of novel bicyclic analogues derived from a potent oxytocin antagonist

O. Chaloin, G. Flouret, J. Slaninová, 2006, Journal of peptide science : an official publication of the European Peptide Society.

Antagonists of oxytocin featuring replacement with modified β‐mercaptopropionic acids at position 1

O. Chaloin, G. Flouret, W. Brieher, 2002, Journal of peptide science : an official publication of the European Peptide Society.

Weak oxytocin agonist converted to highly potent oxytocin antagonist through bicyclization

V. Hruby, J. Slaninová, P. Hill, 1988 .

Magnesium and biological activity of oxytocin analogues modified on aromatic ring of amino acid in position 2

J. Vondrášek, J. Slaninová, L. Maletínská, 2001, Journal of peptide science : an official publication of the European Peptide Society.

The analogs of oxytocin and vasopressin with a bulky amino acid in position 2

J. Slaninová, Z. Procházka, 1995 .

Amino Acids and Peptides. Part 226. Amino and Deamino Analogues of 8‐D‐ Homoarginin‐vasopressin with Modified Tyrosine in Position 2: Synthesis and Some Biological Properties.

M. Lebl, T. Barth, J. Slaninová, 1992 .

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.

Prolonged antidiuretic action of vasopressin analogues in relation to their primary structure

T. Barth, J. Slaninová, J. Škopková, 1981 .

Tissue-specific protective properties of lithium: comparison of rat kidney, erythrocytes and brain

M. Alda, P. Svoboda, J. Slaninová, 2021, Naunyn-Schmiedeberg's Archives of Pharmacology.

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.

Production of porcine antibodies with high specificity to [8-D-arginine] deamino-vasopressin (dDAVP)

T. Barth, J. Slaninová, F. Franek, 1977, Experientia.

Synthesis of the carboxy-terminal octapeptide of cholecystokinin (CKK-8) based on incorporation of O 4 -sulfotyrosine by enzymatically catalyzed formation of peptide bonds

V. Čeřovský, K. Jošt, J. Slaninová, 1988 .

Amino Acids and Peptides. Part 204. Synthesis of the Carboxy-Terminal Octapeptide of Cholecystokinin (CCK-8) Based on Incorporation of O4-Sulfotyrosine by Enzymatically Catalyzed Formation of Peptide Bonds.

V. Čeřovský, K. Jošt, J. Slaninová, 1988 .

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.

New potent antimicrobial peptides from the venom of Polistinae wasps and their analogs

V. Čeřovský, L. Bednárová, J. Slaninová, 2008, Peptides.

Structure–activity relationship of CART (cocaine- and amphetamine-regulated transcript) peptide fragments

W. Kowalczyk, J. Slaninová, B. Železná, 2007, Peptides.

Defensin from the ornate sheep tick Dermacentor marginatus and its effect on Lyme borreliosis spirochetes.

L. Grubhoffer, V. Čeřovský, J. Slaninová, 2014, Developmental and comparative immunology.

Analogues of oxytocin antagonists bearing a ureido group in the amino acid side chain at position 4 or 5

O. Chaloin, G. Flouret, J. Slaninová, 2006, Journal of peptide science : an official publication of the European Peptide Society.

Analogs of arginine vasopressin modified in position 3 with (R)-alpha-hydroxymethylphenylalanine.

A. Olma, J. Slaninová, B. Lammek, 1999, The journal of peptide research : official journal of the American Peptide Society.

Melectin: A Novel Antimicrobial Peptide from the Venom of the Cleptoparasitic Bee Melecta albifrons

Z. Voburka, J. Cvačka, V. Čeřovský, 2008, Chembiochem : a European journal of chemical biology.

The discovery of new potent non-peptide Angiotensin II AT1 receptor blockers: a concise synthesis, molecular docking studies and biological evaluation of N-substituted 5-butylimidazole derivatives.

G. Liapakis, S. Durdağı, J. Matsoukas, 2012, European journal of medicinal chemistry.

Toxicity study of antimicrobial peptides from wild bee venom and their analogs toward mammalian normal and cancer cells

V. Čeřovský, J. Slaninová, L. Monincová, 2012, Peptides.

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.

Synthesis, Bioassay and NMR Study of Methyleneoxy Isosters of Oxytocin and Vasopressin

J. Slaninová, M. Buděšínský, J. Hlaváček, 2002 .

Contribution to characterization of anorectic protein similar to satietin from urine

J. Slaninová, L. Maletínská, 1995, Pharmacology Biochemistry and Behavior.

Antimicrobial Peptide from the Wild Bee Hylaeus signatus Venom and Its Analogues: Structure-Activity Study and Synergistic Effect with Antibiotics.

V. Veverka, V. Čeřovský, L. Bednárová, 2016, Journal of natural products.

The synthesis and opioid receptor binding affinities of analogues of dermorphin and its N-terminal tetrapeptide fragment with dibasic acids in position 2.

V. Hruby, A. Lipkowski, A. Misicka, 1995, Life sciences.

The synthesis and opioid receptor binding affinities of dermorphin and deltorphin analogs with dibasic amino acids in position 2

R. Horváth, V. Hruby, A. Lipkowski, 1993 .

New analogs of arginine-vasopressin containing β-homo-L-amino acid residues

T. Barth, J. Slaninová, K. Bańkowski, 1989 .

Synthesis and biological properties of vasopressin analogues containing 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

M. Lebl, T. Barth, A. Machová, 1990 .

Oxytocin Analogues with O-Glycosylated Serine and Threonine in Position 4

J. Slaninová, Z. Grzonka, A. Marcinkowska, 2007 .

Lysine-Vasopressin Analogues with Glycoconjugates in Position 8

J. Slaninová, Z. Grzonka, A. Marcinkowska, 2006 .

Synthesis and biological properties of cholecystokinin heptapeptide analogues containing D- and L-forms of tert-leucine or neopentylglycine in position 5

J. Slaninová, L. Maletínská, J. Hlaváček, 1991 .

Comparison of anorectic, analgetic and sedative activities of cholecystokinin heptapeptide 27–33 analogues modified in the C-terminal part

J. Slaninová, L. Maletínská, J. Hlaváček, 1993 .

Conformationally restricted analogs of oxytocin; stabilization of inhibitory conformation.

M. Lebl, V. Hruby, W. Kazmierski, 2009, International journal of peptide and protein research.

Inhibitors of Nα-acetyl-l-ornithine deacetylase: synthesis, characterization and analysis of their inhibitory potency

J. Pícha, J. Slaninová, M. Buděšínský, 2010, Amino Acids.

Conformationally restricted analogs of oxytocin; stabilization of inhibitory conformation.

W. Kazmierski, J. Slaninová, Victor J. Hruby, 2009 .

Synthesis of methylated phenylalanines via hydrogenolysis of corresponding 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids. Synthesis and biological activity of oxytocin analogs with methylated phenylalanines in position 2.

M. Lebl, J. Slaninová, P. Majer, 2009, International journal of peptide and protein research.

Conformationally biased analogs of oxytocin.

M. Lebl, V. Hruby, J. Slaninová, 2009, International journal of peptide and protein research.

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 a potent oxytocin antagonist with truncated c‐terminus or shorter amino acid side chain of the basic amino acid at position 8

O. Chaloin, G. Flouret, J. Slaninová, 2003, Journal of peptide science : an official publication of the European Peptide Society.

Utilization of some non coded amino acids as isosters of peptide building blocks

J. Slaninová, J. Hlaváček, J. Slaninová, 1996, Amino Acids.