I. Schepetkin

发表

Osteoblastic differentiation of mesenchymal stem cells by mumie extract

A. Khlebnikov, Cho-Rok Jung, B. Kwon, 2002 .

Complement‐fixing activity of fulvic acid from Shilajit and other natural sources

M. Jutila, G. Xie, M. Quinn, 2009, Phytotherapy research : PTR.

Further modifications of 1H‐pyrrolo[2,3‐b]pyridine derivatives as inhibitors of human neutrophil elastase

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2019, Drug development research.

1H-pyrrolo[2,3-b]pyridine: A new scaffold for human neutrophil elastase (HNE) inhibitors.

E. Teodori, A. Khlebnikov, C. Vergelli, 2018, Bioorganic & medicinal chemistry.

Cinnoline derivatives as human neutrophil elastase inhibitors

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2016, Journal of enzyme inhibition and medicinal chemistry.

Synthesis of Five‐ and Six‐Membered N‐Phenylacetamido Substituted Heterocycles as Formyl Peptide Receptor Agonists

R. Ye, C. Vergelli, M. Giovannoni, 2017, Drug development research.

2-Arylacetamido-4-phenylamino-5-substituted pyridazinones as formyl peptide receptors agonists.

R. Ye, A. Khlebnikov, C. Vergelli, 2016, Bioorganic & medicinal chemistry.

Immunomodulatory activity of polysaccharides isolated from Alchornea cordifolia.

M. Jutila, A. Yapi, M. Quinn, 2013, Journal of ethnopharmacology.

Immunomodulatory activity of polysaccharides isolated from Clerodendrum splendens: Beneficial effects in experimental autoimmune encephalomyelitis

M. Jutila, D. Khramova, A. Yapi, 2013, BMC Complementary and Alternative Medicine.

Development of small molecule non-peptide formyl peptide receptor (FPR) ligands and molecular modeling of their recognition.

A. Khlebnikov, M. Giovannoni, A. Cilibrizzi, 2014, Current medicinal chemistry.

Computational structure-activity relationship analysis of small-molecule agonists for human formyl peptide receptors.

A. Khlebnikov, M. Quinn, I. Schepetkin, 2010, European journal of medicinal chemistry.

Computational structure-activity relationship analysis of non-peptide inducers of macrophage tumor necrosis factor-alpha production.

A. Khlebnikov, M. Quinn, I. Schepetkin, 2008, Bioorganic & medicinal chemistry.

Structure-activity relationship analysis of N-benzoylpyrazoles for elastase inhibitory activity: a simplified approach using atom pair descriptors.

A. Khlebnikov, M. Quinn, I. Schepetkin, 2008, Bioorganic & medicinal chemistry.

Electrosprayed poly(lactic-co-glycolic acid) particles as a promising drug delivery system for the novel JNK inhibitor IQ-1.

E. Bolbasov, K. Stankevich, S. Tverdokhlebov, 2020, European polymer journal.

Decomposition of reactive oxygen species by copper(II) bis(1-pyrazolyl)methane complexes

A. Khlebnikov, E. Korotkova, G. Malovichko, 2006, JBIC Journal of Biological Inorganic Chemistry.

Macrophage immunomodulatory activity of polysaccharides isolated from Opuntia polyacantha.

M. Jutila, G. Xie, M. Quinn, 2008, International immunopharmacology.

Botanical polysaccharides: macrophage immunomodulation and therapeutic potential.

M. Quinn, Igor A Schepetkin, Mark T Quinn, 2006, International immunopharmacology.

Polysaccharides Isolated from Açaí Fruit Induce Innate Immune Responses

J. Holderness, J. Hedges, B. Freedman, 2011, PloS one.

Immunomodulatory Activity of Oenothein B Isolated from Epilobium angustifolium1

M. Jutila, A. Khlebnikov, M. Quinn, 2009, The Journal of Immunology.

Fractionation and characterization of biologically-active polysaccharides from Artemisia tripartita.

G. Xie, M. Quinn, I. Schepetkin, 2008, Phytochemistry.

Immunomodulatory activity of acidic polysaccharides isolated from Tanacetum vulgare L.

G. Xie, M. Quinn, I. Schepetkin, 2007, International immunopharmacology.

Macrophage immunomodulatory activity of polysaccharides isolated from Juniperus scopolorum.

M. Quinn, I. Schepetkin, J. Wiley, 2005, International immunopharmacology.

Molecular Mechanisms for Regulation of Neutrophil Apoptosis under Normal and Pathological Conditions

D. Atochin, I. Schepetkin, E. M. Noseykina, 2021, Journal of Evolutionary Biochemistry and Physiology.

Synthesis, characterization and potent superoxide dismutase-like activity of novel bis(pyrazole)-2,2'-bipyridyl mixed ligand copper(II) complexes.

A. Khlebnikov, M. Quinn, A. Potapov, 2009, Dalton transactions.

Identification of Novel Formyl Peptide Receptor-Like 1 Agonists That Induce Macrophage Tumor Necrosis Factor α Production

R. Ye, A. Khlebnikov, Jun Tian, 2008, Molecular Pharmacology.

Osteoclastic Bone Resorption: Normal and Pathological

I. Schepetkin, Igor Schepetkin, 1997, Annals of the New York Academy of Sciences.

1,5,6,7-Tetrahydro-4H-indazol-4-ones as human neutrophil elastase (HNE) inhibitors.

G. Bartolucci, E. Teodori, C. Vergelli, 2021, Bioorganic & medicinal chemistry letters.

Poly(ε-caprolactone) Scaffolds Doped with c-Jun N-terminal Kinase Inhibitors Modulate Phagocyte Activation.

K. Stankevich, S. Goreninskii, S. Tverdokhlebov, 2019, ACS biomaterials science & engineering.

Therapeutic Effects of Tryptanthrin and Tryptanthrin-6-Oxime in Models of Rheumatoid Arthritis

D. Hammaker, A. Khlebnikov, M. Quinn, 2020, Frontiers in Pharmacology.

Characterization and biological activities of humic substances from mumie.

B. Kwon, A. Khlebnikov, I. Schepetkin, 2003, Journal of agricultural and food chemistry.

Decreased luminol-dependent chemiluminescence response of neutrophils to recombinant human tumour necrosis factor in patients with gastric cancer

I. Schepetkin, N. Cherdyntseva, E. Borunov, 2005, Journal of Cancer Research and Clinical Oncology.

Pyridazinones and Structurally Related Derivatives with Anti-Inflammatory Activity

A. Khlebnikov, M. Giovannoni, M. Quinn, 2022, Molecules.

Pyridinone Derivatives as Interesting Formyl Peptide Receptor (FPR) Agonists for the Treatment of Rheumatoid Arthritis

C. Ghelardini, E. Lucarini, L. di Cesare Mannelli, 2021, Molecules.

Novel formyl peptide receptors (FPRs) agonists with pyridinone and pyrimidindione scaffolds that are potentially useful for the treatment of rheumatoid arthritis.

C. Ghelardini, C. Parisio, L. di Cesare Mannelli, 2020, Bioorganic chemistry.

E. Lacivita, M. Leopoldo, M. Quinn, 2019, MedChemComm.

Novel ureidopropanamide based N-formyl peptide receptor 2 (FPR2) agonists with potential application for central nervous system disorders characterized by neuroinflammation.

E. Lacivita, M. Leopoldo, R. Perrone, 2017, European journal of medicinal chemistry.

Antagonism of human formyl peptide receptor 1 with natural compounds and their synthetic derivatives.

A. Khlebnikov, M. Quinn, I. Schepetkin, 2016, International immunopharmacology.

Novel 3-(1H-indol-3-yl)-2-[3-(4-methoxyphenyl)ureido]propanamides as selective agonists of human formyl-peptide receptor 2.

E. Lacivita, M. Leopoldo, R. Perrone, 2015, Bioorganic & medicinal chemistry.

Antagonism of human formyl peptide receptor 1 (FPR1) by chromones and related isoflavones.

R. Ye, A. Khlebnikov, M. Quinn, 2014, Biochemical pharmacology.

Synthesis, HPLC enantioresolution, and X-ray analysis of a new series of C5-methyl pyridazines as N-formyl peptide receptor (FPR) agonists.

G. Bartolucci, C. Vergelli, M. Giovannoni, 2013, Chirality.

Synthesis, enantioresolution, and activity profile of chiral 6-methyl-2,4-disubstituted pyridazin-3(2H)-ones as potent N-formyl peptide receptor agonists.

G. Bartolucci, C. Vergelli, M. Giovannoni, 2012, Bioorganic & medicinal chemistry.

Identification of Novel Small-Molecule Agonists for Human Formyl Peptide Receptors and Pharmacophore Models of Their Recognition

M. Jutila, R. Ye, A. Khlebnikov, 2010, Molecular Pharmacology.

High-Throughput Screening for Small-Molecule Activators of Neutrophils: Identification of Novel N-Formyl Peptide Receptor Agonists

A. Khlebnikov, M. Quinn, I. Schepetkin, 2007, Molecular Pharmacology.

6-methyl-2,4-disubstituted pyridazin-3(2H)-ones: a novel class of small-molecule agonists for formyl peptide receptors.

J. Holderness, R. Ye, C. Vergelli, 2009, Journal of medicinal chemistry.

Nicotinamide Glycolates Antagonize CXCR2 Activity through an Intracellular Mechanism

M. Quinn, J. Zebala, D. Maeda, 2010, Journal of Pharmacology and Experimental Therapeutics.

The experimental model of type 2 diabetes mellitus caused by a high-fat diet with low-dose streptozotocin in rats

V. V. Ivanov, I. Schepetkin, E. Buyko, 2020, Bulletin of Siberian Medicine.

Neuroprotective Effects of the Lithium Salt of a Novel JNK Inhibitor in an Animal Model of Cerebral Ischemia–Reperfusion

A. Khlebnikov, E. Plotnikov, M. Quinn, 2022, Biomedicines.

Neuroprotective Effects of a Novel Inhibitor of c-Jun N-Terminal Kinase in the Rat Model of Transient Focal Cerebral Ischemia

D. Atochin, A. Khlebnikov, I. Schepetkin, 2020, Cells.

c-Jun N-Terminal Kinases (JNKs) in Myocardial and Cerebral Ischemia/Reperfusion Injury

D. Atochin, E. Atochina-Vasserman, I. Schepetkin, 2018, Front. Pharmacol..

Design, synthesis and biological evaluation of novel O-substituted tryptanthrin oxime derivatives as c-Jun N-terminal kinase inhibitors

A. Khlebnikov, M. Quinn, M. Cook, 2022, Frontiers in Pharmacology.

Osteoblastic Differentiation of Mesenchymal Stem Cells by

A. Khlebnikov, Cho-Rok Jung, B. Kwon, 2002 .

Inhibitory effect of IQ-1S, a selective c-Jun N-terminal kinase (JNK) inhibitor, on phenotypical and cytokine-producing characteristics in human macrophages and T-cells.

D. Atochin, G. Seledtsova, I. Schepetkin, 2020, European journal of pharmacology.

Aging influences the response of T cells to stimulation by the ellagitannin, oenothein B.

M. Jutila, M. Quinn, I. Schepetkin, 2015, International immunopharmacology.

Synthesis, Biological Evaluation, and Molecular Modeling of Aza-Crown Ethers

A. Khlebnikov, T. Kirichenko, M. Quinn, 2021, Molecules.

Synthesis, anticancer activity, and molecular modeling of 1,4-naphthoquinones that inhibit MKK7 and Cdc25.

Igor A. Levandovskiy, A. Khlebnikov, M. Quinn, 2019, European journal of medicinal chemistry.

4‐Aroyl‐3‐hydroxy‐5‐phenyl‐1H‐pyrrol‐2(5H)‐ones as N‐formyl peptide receptor 1 (FPR1) antagonists

R. Ye, A. Khlebnikov, D. Kominsky, 2017, Biochemical pharmacology.

Physicochemical Characterization and Antioxidant Activity of Humic Acids Isolated from Peat of Various Origins

M. Yusubov, M. Quinn, I. Schepetkin, 2018, Molecules.

Immunomodulatory and hemagglutinating activities of acidic polysaccharides isolated from Combretum racemosum.

M. Jutila, A. Yapi, M. Quinn, 2013, International immunopharmacology.

Synthesis and Pharmacological Evaluation of New Pyridazin‐Based Thioderivatives as Formyl Peptide Receptor (FPR) Agonists

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2013 .

Synthesis and Cytotoxicity of bis(pyrazol-1-yl)-Alkane Derivatives with Polymethylene Linkers and Related Mono- and Dipyrazolium Salts

A. Khlebnikov, T. Petrenko, A. Potapov, 2016, Chemistry of Heterocyclic Compounds.

Neutrophil Immunomodulatory Activity of Nerolidol, a Major Component of Essential Oils from Populus balsamifera Buds and Propolis

A. Khlebnikov, T. Özek, M. Quinn, 2022, Plants.

Chemical composition and phagocyte immunomodulatory activity of Ferula iliensis essential oils

A. Khlebnikov, M. Quinn, I. Schepetkin, 2017, Journal of leukocyte biology.

Neutrophil Immunomodulatory Activity of Farnesene, a Component of Artemisia dracunculus Essential Oils

A. Khlebnikov, T. Özek, M. Quinn, 2022, Pharmaceuticals.

Further studies on 2-arylacetamide pyridazin-3(2H)-ones: design, synthesis and evaluation of 4,6-disubstituted analogs as formyl peptide receptors (FPRs) agonists.

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2013, European journal of medicinal chemistry.

Synthesis, biological evaluation, and molecular modeling of 11H-indeno[1,2-b]quinoxalin-11-one derivatives and tryptanthrin-6-oxime as c-Jun N-terminal kinase inhibitors.

D. Atochin, A. Khlebnikov, M. Quinn, 2019, European journal of medicinal chemistry.

Identification and Characterization of a Novel Class of c-Jun N-terminal Kinase Inhibitors

Irina Kochetkova, Irina A. Kochetkova, M. Jutila, 2012, Molecular Pharmacology.

Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold

A. Khlebnikov, I. Bagryanskaya, M. Quinn, 2021, Molecules.

Exploration of nitrogen heterocycle scaffolds for the development of potent human neutrophil elastase inhibitors.

G. Bartolucci, G. Floresta, A. Khlebnikov, 2020, Bioorganic & medicinal chemistry.

Optimization of N-benzoylindazole derivatives as inhibitors of human neutrophil elastase.

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2013, Journal of medicinal chemistry.

Design, synthesis and evaluation of N-benzoylindazole derivatives and analogues as inhibitors of human neutrophil elastase.

A. Khlebnikov, V. D. Piaz, C. Vergelli, 2011, Bioorganic & medicinal chemistry.

N-Benzoylpyrazoles Are Novel Small-Molecule Inhibitors of Human Neutrophil Elastase

A. Khlebnikov, M. Quinn, I. Schepetkin, 2007 .

Oximes: Novel Therapeutics with Anticancer and Anti-Inflammatory Potential

A. Khlebnikov, M. Quinn, I. Schepetkin, 2021, Biomolecules.

A patenting perspective on human neutrophil elastase (HNE) inhibitors (2014-2018) and their therapeutic applications

M. Giovannoni, M. Quinn, I. Schepetkin, 2019, Expert opinion on therapeutic patents.

Essential Oils from Monarda fistulosa: Chemical Composition and Activation of Transient Receptor Potential A1 (TRPA1) Channels

A. Khlebnikov, T. Özek, M. Quinn, 2020, Molecules.

Fulvic acid fractions from mumie

A. Khlebnikov, I. Schepetkin, S. Woo, 2004, Proceedings. The 8th Russian-Korean International Symposium on Science and Technology, 2004. KORUS 2004..

Medical drugs from humus matter: Focus on mumie

B. Kwon, A. Khlebnikov, I. Schepetkin, 2002 .

Innate Immunomodulatory Activity of Cedrol, a Component of Essential Oils Isolated from Juniperus Species.

A. Khlebnikov, T. Özek, M. Quinn, 2021, Molecules.

Novel innate polysaccharide agonists derived from Funtumia elastica tree bark (Yamoa™)

J. Graff, J. Hedges, B. Freedman, 2008 .

Neutrophil Immunomodulatory Activity of (−)-Borneol, a Major Component of Essential Oils Extracted from Grindelia squarrosa

A. Khlebnikov, T. Özek, M. Quinn, 2022, Molecules.

Chemical Composition and Immunomodulatory Activity of Essential Oils from Rhododendron albiflorum

A. Khlebnikov, T. Özek, M. Quinn, 2021, Molecules.

Chemical Composition and Immunomodulatory Activity of Hypericum perforatum Essential Oils †

A. Khlebnikov, T. Özek, M. Quinn, 2020, Biomolecules.

Inhibition of T Cell Receptor Activation by Semi-Synthetic Sesquiterpene Lactone Derivatives and Molecular Modeling of Their Interaction with Glutathione and Tyrosine Kinase ZAP-70

S. Adekenov, A. Khlebnikov, M. Quinn, 2019, Molecules.

The natural sesquiterpene lactones arglabin, grosheimin, agracin, parthenolide, and estafiatin inhibit T cell receptor (TCR) activation.

S. Adekenov, M. Quinn, I. Schepetkin, 2018, Phytochemistry.

Modulation of Human Neutrophil Responses by the Essential Oils from Ferula akitschkensis and Their Constituents.

P. Sinharoy, A. Khlebnikov, T. Özek, 2016, Journal of agricultural and food chemistry.

Inhibition of Human Neutrophil Responses by the Essential Oil of Artemisia kotuchovii and Its Constituents.

K. Başer, T. Özek, M. Quinn, 2015, Journal of agricultural and food chemistry.

Design, Synthesis, Biological Evaluation, and Computational Studies of Novel Ureidopropanamides as Formyl Peptide Receptor 2 (FPR2) Agonists to Target the Resolution of Inflammation in Central Nervous System Disorders.

E. Lacivita, M. Leopoldo, Mauro Niso, 2022, Journal of medicinal chemistry.

Neutrophil Immunomodulatory Activity of Natural Organosulfur Compounds

A. Khlebnikov, M. Quinn, I. Schepetkin, 2019, Molecules.

Chemical Composition and Antibacterial Activity of Essential Oils from Ferula L. Species against Methicillin-Resistant Staphylococcus aureus

J. Voyich, T. Özek, M. Quinn, 2018, Molecules.

N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase.

A. Khlebnikov, M. Quinn, I. Schepetkin, 2007, Journal of medicinal chemistry.

Therapeutic Potential of Polyphenols from Epilobium Angustifolium (Fireweed)

M. Jutila, J. Voyich, M. Quinn, 2016, Phytotherapy research : PTR.

Synthesis, biological evaluation, molecular modeling, and structural analysis of new pyrazole and pyrazolone derivatives as N‐formyl peptide receptors agonists

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2021, Chemical biology & drug design.

3-(1H-indol-3-yl)-2-[3-(4-nitrophenyl)ureido]propanamide enantiomers with human formyl-peptide receptor agonist activity: molecular modeling of chiral recognition by FPR2.

E. Lacivita, M. Leopoldo, A. Khlebnikov, 2013, Biochemical pharmacology.

Gastrin-Releasing Peptide/Neuromedin B Receptor Antagonists PD176252, PD168368, and Related Analogs Are Potent Agonists of Human Formyl-Peptide Receptors

M. Jutila, A. Khlebnikov, M. Quinn, 2011, Molecular Pharmacology.

Functional N‐Formyl Peptide Receptor 2 (FPR2) Antagonists Based on the Ureidopropanamide Scaffold Have Potential To Protect Against Inflammation‐Associated Oxidative Stress

E. Lacivita, M. Leopoldo, R. Perrone, 2017, ChemMedChem.

Molecular docking of 2-(benzimidazol-2-ylthio)-N-phenylacetamide-derived small-molecule agonists of human formyl peptide receptor 1

M. Jutila, A. Khlebnikov, C. Dahlgren, 2012, Journal of Molecular Modeling.

Modeling of the anticancer action for radical derivatives of nitroazoles: quantitative structure-activity relationship (QSAR) study.

B. Kwon, A. Khlebnikov, I. Schepetkin, 2002, Cancer biotherapy & radiopharmaceuticals.

Sanazole as substrate of xanthine oxidase and microsomal NADPH/cytochrome P450 reductase.

I. Schepetkin, N. Cherdyntseva, V. Kagiya, 2001, Pathophysiology : the official journal of the International Society for Pathophysiology.

Improved quantitative structure-activity relationship models to predict antioxidant activity of flavonoids in chemical, enzymatic, and cellular systems.

A. Khlebnikov, M. Quinn, Andrei I Khlebnikov, 2007, Bioorganic & medicinal chemistry.

Anti-Inflammatory Effects and Joint Protection in Collagen-Induced Arthritis after Treatment with IQ-1S, a Selective c-Jun N-Terminal Kinase Inhibitor

G. Firestein, D. Hammaker, A. Khlebnikov, 2015, The Journal of Pharmacology and Experimental Therapeutics.

Therapeutic Effect of Novel Cyanopyrrolidine-Based Prolyl Oligopeptidase Inhibitors in Rat Models of Amnesia

A. Khlebnikov, T. Voronina, M. Quinn, 2021, Frontiers in Chemistry.

Protective Effects of a New C-Jun N-terminal Kinase Inhibitor in the Model of Global Cerebral Ischemia in Rats

D. Atochin, A. Khlebnikov, I. Schepetkin, 2019, Molecules.

Oenothein B, a Cyclic Dimeric Ellagitannin Isolated from Epilobium angustifolium, Enhances IFNγ Production by Lymphocytes

M. Jutila, M. Quinn, I. Schepetkin, 2012, PloS one.

Suppression by radiosensitizer AK-2123 of early phorbol myristate acetate-stimulated chemiluminescence response of human neutrophils induced by gamma-irradiation (short communication).

I. Schepetkin, 1998, Cancer biotherapy & radiopharmaceuticals.

Role of NADPH Oxidase in Formation and Function of Multinucleated Giant Cells

M. Quinn, I. Schepetkin, 2009, Journal of Innate Immunity.

Isoxazol-5(2H)-one: a new scaffold for potent human neutrophil elastase (HNE) inhibitors

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2017, Journal of enzyme inhibition and medicinal chemistry.

Cardioprotective Effects of a Selective c-Jun N-terminal Kinase Inhibitor in a Rat Model of Myocardial Infarction

D. Atochin, A. Khlebnikov, M. Quinn, 2023, Biomedicines.

Quantitative structure-activity relationships for small non-peptide antagonists of CXCR2: indirect 3D approach using the frontal polygon method.

A. Khlebnikov, M. Quinn, I. Schepetkin, 2006, Bioorganic & medicinal chemistry.

Novel Sulfonamide Analogs of Sivelestat as Potent Human Neutrophil Elastase Inhibitors

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2020, Frontiers in Chemistry.

New 3‐unsubstituted isoxazolones as potent human neutrophil elastase inhibitors: Synthesis and molecular dynamic simulation

E. Teodori, C. Vergelli, M. Giovannoni, 2019, Drug development research.

Alarmins and c-Jun N-Terminal Kinase (JNK) Signaling in Neuroinflammation

D. Atochin, M. Quinn, I. Schepetkin, 2020, Cells.

Synthesis, biological evaluation, and molecular modelling studies of potent human neutrophil elastase (HNE) inhibitors

G. Bartolucci, Marta Menicatti, C. Vergelli, 2018, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and analytical characterization of new thiazol-2-(3H)-ones as human neutrophil elastase (HNE) inhibitors

G. Bartolucci, Marta Menicatti, A. Khlebnikov, 2017, Chemistry Central Journal.

Synthesis and Pharmacological Evaluation of Indole Derivatives as Deaza Analogues of Potent Human Neutrophil Elastase Inhibitors

A. Khlebnikov, C. Vergelli, M. Giovannoni, 2016, Drug development research.

Polysaccharides derived from Yamoa (Funtumia elastica) prime gammadelta T cells in vitro and enhance innate immune responses in vivo.

J. Holderness, J. Graff, J. Hedges, 2009, International immunopharmacology.

Different Metabolic Effects of Ganglioside GM1 in Brain Synaptosomes and Phagocytic Cells

Y. Tyurina, V. Tyurin, I. Gamaley, 2002, Neurochemical Research.

Immune response to haptenized tumor antigen as possible mechanism of anticancer action of hypoxic bioreductive agents at low doses.

I. Schepetkin, 1999, Cancer biotherapy & radiopharmaceuticals.

Antihypertensive activity of a new c-Jun N-terminal kinase inhibitor in spontaneously hypertensive rats

D. Atochin, A. Khlebnikov, I. Schepetkin, 2020, Hypertension Research.

Inhibition of Acetylcholinesterase by Novel Lupinine Derivatives

A. Khlebnikov, M. Quinn, I. Schepetkin, 2023, Molecules.

Neutrophil isolation from nonhuman species.

Adeline R. Whitney, B. Lei, F. DeLeo, 2014, Methods in molecular biology.

Neutrophil isolation from nonhuman species.

Benfang Lei, B. Lei, M. Quinn, 2007, Methods in molecular biology.

Novel small-molecule inhibitors of anthrax lethal factor identified by high-throughput screening.

A. Khlebnikov, M. Quinn, I. Schepetkin, 2006, Journal of medicinal chemistry.

Synthesis and biological activity of hydrazones of o- and p-hydroxybenzoic acids. Spatial structure of 5-Bromo-2-hydroxybenzylidene-4-hydroxybenzohydrazide

K. M. Turdybekov, A. Khlebnikov, I. Schepetkin, 2017, Russian Journal of General Chemistry.

Nasal Acai Polysaccharides Potentiate Innate Immunity to Protect against Pulmonary Francisella tularensis and Burkholderia pseudomallei Infections

J. Holderness, M. Jutila, S. Dow, 2012, PLoS pathogens.

Isolation of Neutrophils from Nonhuman Species.

B. Lei, F. DeLeo, Natalia Małachowa, 2020, Methods in molecular biology.

Novel Tryptanthrin Derivatives with Selectivity as c–Jun N–Terminal Kinase (JNK) 3 Inhibitors

A. Khlebnikov, M. Quinn, I. Schepetkin, 2023, Molecules.

Composition and Biological Activity of the Essential Oils from Wild Horsemint, Yarrow, and Yampah from Subalpine Meadows in Southwestern Montana: Immunomodulatory Activity of Dillapiole

A. Khlebnikov, T. Özek, M. Quinn, 2023, Plants.

A novel dual NO-donating oxime and c-Jun N-terminal kinase inhibitor protects against cerebral ischemia–reperfusion injury in mice

D. Atochin, Paul L Huang, A. Khlebnikov, 2016, Neuroscience Letters.

Neuroprotective Effects of Tryptanthrin-6-Oxime in a Rat Model of Transient Focal Cerebral Ischemia

D. Atochin, A. Khlebnikov, E. Plotnikov, 2023, Pharmaceuticals.