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Theoretical Studies of Leu-Pro-Arg-Asp-Ala Pentapeptide (LPRDA) Binding to Sortase A of Staphylococcus aureus

Molecules (Basel, Switzerland), 2022-11, Vol.27 (23), p.8182

2022

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Selection of Promising Novel Fragment Sized S. aureus SrtA Noncovalent Inhibitors Based on QSAR and Docking Modeling Studies

Molecules (Basel, Switzerland), 2021-12, Vol.26 (24), p.7677

2021

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Oligopeptide Sortase Inhibitor Modulates Staphylococcus aureus Cell Adhesion and Biofilm Formation

Antibiotics (Basel), 2022-12, Vol.11 (12), p.1836

2022

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Alternating Asymmetric Self-Induction in Functionalized Pyrrolidine Oligomers

Angewandte Chemie International Edition, 2013-11, Vol.52 (48), p.12736-12740

International ed. in English, 2013

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Probing of the cis-5-phenyl proline scaffold as a platform for the synthesis of mechanism-based inhibitors of the Staphylococcus aureus sortase SrtA isoform

Bioorganic & medicinal chemistry, 2009-04, Vol.17 (7), p.2886-2893

2009

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Ensemble Docking as a Tool for the Rational Design of Peptidomimetic Staphylococcus aureus Sortase A Inhibitors

International journal of molecular sciences, 2024-10, Vol.25 (20), p.11279

2024

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Pyrrolidine/Azepane Ring Expansion via Intramolecular Ullmann-Type Annulation/Rearrangement Cascade: Synthesis of Highly Functionalized 1H‑Benzazepines

Organic letters, 2023-10, Vol.25 (41), p.7573-7577

2023

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Theoretical and NMR Conformational Studies of β-Proline Oligopeptides With Alternating Chirality of Pyrrolidine Units

Frontiers in chemistry, 2018-03, Vol.6, p.91

2018

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Pharmacological Correction of Stress-Induced Gastric Ulceration by Novel Small-Molecule Agents with Antioxidant Profile

TheScientificWorld, 2014-01, Vol.2014 (2014), p.1-6

2014

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Chemoselectivity issues of the asymmetric interaction between cyclohexanone, β‐nitrostyrene, and benzoic acid under 5‐aryl prolinate's organocatalysis

Chirality (New York, N.Y.), 2020-06, Vol.32 (6), p.833-841

2020

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Interplay of Pyrrolidine Units with Homo/Hetero Chirality and CF3–Aryl Substituents on Secondary Structures of β‑Proline Tripeptides in Solution

Journal of organic chemistry, 2020-07, Vol.85 (14), p.8865-8871

2020

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Solution NMR Studies of LPRDA Peptide: an Oligopeptide Inhibitor of Staphylococcus aureus Sortase A

Applied magnetic resonance, 2024-04, Vol.55 (4), p.451-461

2024

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4-[(1RS,5RS,7SR)-5-Methyl-2,4-dioxo-3,6-diaza-bicyclo-[3.2.1]octan-7-yl]benzonitrile

Acta crystallographica. Section E, Structure reports online, 2012-06, Vol.68 (Pt 6), p.o1718-o1718

2012

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Interplay of Pyrrolidine Units with Homo/Hetero Chirality and CF 3 -Aryl Substituents on Secondary Structures of β-Proline Tripeptides in Solution

Journal of organic chemistry, 2020-07, Vol.85 (14), p.8865-8871

2020

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Control of Azomethine Cycloaddition Stereochemistry by CF3 Group: Structural Diversity of Fluorinated β‑Proline Dimers

Organic letters, 2016-09, Vol.18 (18), p.4698-4701

2016

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Menthols as Chiral Auxiliaries for Asymmetric Cycloadditive Oligomerization: Syntheses and Studies of β‑Proline Hexamers

Organic letters, 2015-12, Vol.17 (24), p.6178-6181

2015

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Efficient Synthesis of Functionalized Diazacyclopenta[c]pentalene with Multiple Intermolecular Interactions in Crystal

Heterocycles, 2011, Vol.83 (2), p.323

V. Kudryavtsev, Konstantin

2011

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Crystal structure of 4-[(1 R ,2 S ,5 R )-2-isopropyl-5-methylcyclohexyl] 2-methyl (2 S ,4 S ,5 R )-1-[(2 S ,3 R ,5 R )-5-methoxycarbonyl-2-(2-methylphenyl)pyrrolidine-3-carbonyl]-5-(2-methylphenyl)pyrrolidine-2,4-dicarboxylate

Acta crystallographica. Section E, Crystallographic communications, 2019-05, Vol.75 (5), p.537-539

2019

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Enantiomerically pure β-dipeptide derivative induces anticancer activity against human hormone-refractory prostate cancer through both PI3K/Akt-dependent and -independent pathways

Oncotarget, 2017-11, Vol.8 (57), p.96668-96683

2017

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Structural Studies and Anticancer Activity of a Novel Class of β-Peptides

Chemistry, an Asian journal, 2015-02, Vol.10 (2), p.383-389

2015

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Crystal structure of 4-[(1 R ,2 S ,5 R )-2-isopropyl-5-methyl-cyclo-hex-yl] 2-methyl (2 S ,4 S ,5 R )-1-[(2 S ,3 R ,5 R )-5-meth-oxy-carbonyl-2-(2-methyl-phen-yl)pyrrolidine-3-carbon-yl]-5-(2-methyl-phen-yl)pyrrolidine-2,4-di-carboxyl-ate

Acta crystallographica. Section E, Crystallographic communications, 2019-05, Vol.75 (Pt 5), p.537-539

2019

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Theoretical Studies of Leu-Pro-Arg-Asp-Ala Pentapeptide Binding to Sortase A of IStaphylococcus aureus/I

Molecules (Basel, Switzerland), 2022-11, Vol.27 (23)

2022

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KUD773, a phenylthiazole derivative, displays anticancer activity in human hormone-refractory prostate cancers through inhibition of tubulin polymerization and anti-Aurora A activity

Journal of biomedical science, 2015-01, Vol.22 (1), p.2-2, Article 2

2015

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Pyrrolidine/Azepane Ring Expansion via Intramolecular Ullmann-Type Annulation/Rearrangement Cascade: Synthesis of Highly Functionalized 1 H -Benzazepines

Organic letters, 2023-10, Vol.25 (41), p.7573-7577

2023

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2-(1 H -Imidazol-1-yl)-4-[3-(trifluoromethyl)phenyl]-1,3-thiazole

Acta crystallographica. Section E, Structure reports online, 2013-02, Vol.69 (2), p.o238-o238

2013

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Theoretical Studies of Leu-Pro-Arg-Asp-Ala Pentapeptide (LPRDA) Binding to Sortase A of Staphylococcus aureus

Selection of Promising Novel Fragment Sized S. aureus SrtA Noncovalent Inhibitors Based on QSAR and Docking Modeling Studies

Oligopeptide Sortase Inhibitor Modulates Staphylococcus aureus Cell Adhesion and Biofilm Formation

Alternating Asymmetric Self-Induction in Functionalized Pyrrolidine Oligomers

Probing of the cis-5-phenyl proline scaffold as a platform for the synthesis of mechanism-based inhibitors of the Staphylococcus aureus sortase SrtA isoform

Ensemble Docking as a Tool for the Rational Design of Peptidomimetic Staphylococcus aureus Sortase A Inhibitors

Pyrrolidine/Azepane Ring Expansion via Intramolecular Ullmann-Type Annulation/Rearrangement Cascade: Synthesis of Highly Functionalized 1H‑Benzazepines

Theoretical and NMR Conformational Studies of β-Proline Oligopeptides With Alternating Chirality of Pyrrolidine Units

Pharmacological Correction of Stress-Induced Gastric Ulceration by Novel Small-Molecule Agents with Antioxidant Profile

Chemoselectivity issues of the asymmetric interaction between cyclohexanone, β‐nitrostyrene, and benzoic acid under 5‐aryl prolinate's organocatalysis

Interplay of Pyrrolidine Units with Homo/Hetero Chirality and CF3–Aryl Substituents on Secondary Structures of β‑Proline Tripeptides in Solution

Solution NMR Studies of LPRDA Peptide: an Oligopeptide Inhibitor of Staphylococcus aureus Sortase A

4-[(1RS,5RS,7SR)-5-Methyl-2,4-dioxo-3,6-diaza-bicyclo-[3.2.1]octan-7-yl]benzonitrile

Interplay of Pyrrolidine Units with Homo/Hetero Chirality and CF 3 -Aryl Substituents on Secondary Structures of β-Proline Tripeptides in Solution

Control of Azomethine Cycloaddition Stereochemistry by CF3 Group: Structural Diversity of Fluorinated β‑Proline Dimers

Menthols as Chiral Auxiliaries for Asymmetric Cycloadditive Oligomerization: Syntheses and Studies of β‑Proline Hexamers

Efficient Synthesis of Functionalized Diazacyclopenta[c]pentalene with Multiple Intermolecular Interactions in Crystal

Crystal structure of 4-[(1 R ,2 S ,5 R )-2-isopropyl-5-methylcyclohexyl] 2-methyl (2 S ,4 S ,5 R )-1-[(2 S ,3 R ,5 R )-5-methoxycarbonyl-2-(2-methylphenyl)pyrrolidine-3-carbonyl]-5-(2-methylphenyl)pyrrolidine-2,4-dicarboxylate

Enantiomerically pure β-dipeptide derivative induces anticancer activity against human hormone-refractory prostate cancer through both PI3K/Akt-dependent and -independent pathways

Structural Studies and Anticancer Activity of a Novel Class of β-Peptides

Crystal structure of 4-[(1 R ,2 S ,5 R )-2-isopropyl-5-methyl-cyclo-hex-yl] 2-methyl (2 S ,4 S ,5 R )-1-[(2 S ,3 R ,5 R )-5-meth-oxy-carbonyl-2-(2-methyl-phen-yl)pyrrolidine-3-carbon-yl]-5-(2-methyl-phen-yl)pyrrolidine-2,4-di-carboxyl-ate

Theoretical Studies of Leu-Pro-Arg-Asp-Ala Pentapeptide Binding to Sortase A of IStaphylococcus aureus/I

KUD773, a phenylthiazole derivative, displays anticancer activity in human hormone-refractory prostate cancers through inhibition of tubulin polymerization and anti-Aurora A activity

Pyrrolidine/Azepane Ring Expansion via Intramolecular Ullmann-Type Annulation/Rearrangement Cascade: Synthesis of Highly Functionalized 1 H -Benzazepines

2-(1 H -Imidazol-1-yl)-4-[3-(trifluoromethyl)phenyl]-1,3-thiazole

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