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Protein Cargo Delivery Properties of Cell-Penetrating Peptides. A Comparative Study

Bioconjugate chemistry, 2004-11, Vol.15 (6), p.1246-1253

2004

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Dissection of Protein Kinase Pathways in Live Cells Using Photoluminescent Probes: Surveillance or Interrogation?

Chemosensors, 2018-06, Vol.6 (2), p.19

2018

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Conjugation of Adenosine and Hexa-(d-arginine) Leads to a Nanomolar Bisubstrate-Analog Inhibitor of Basophilic Protein Kinases

Journal of medicinal chemistry, 2006-11, Vol.49 (24), p.7150-7159

2006

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Construction of Covalent Bisubstrate Inhibitor of Protein Kinase Reacting with Cysteine Residue at Substrate-Binding Site

Journal of medicinal chemistry, 2022-08, Vol.65 (16), p.10975-10991

2022

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Oligo-aspartic acid conjugates with benzo[c][2,6]naphthyridine-8-carboxylic acid scaffold as picomolar inhibitors of CK2

Bioorganic & medicinal chemistry, 2017-04, Vol.25 (7), p.2277-2284

2017

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Thiazole- and selenazole-comprising high-affinity inhibitors possess bright microsecond-scale photoluminescence in complex with protein kinase CK2

Bioorganic & medicinal chemistry, 2018-10, Vol.26 (18), p.5062-5068

2018

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Discovery of strong inhibitory properties of a monoclonal antibody of PKA and use of the antibody and a competitive photoluminescent orthosteric probe for analysis of the protein kinase

Biochimica et biophysica acta. Proteins and proteomics, 2020-08, Vol.1868 (8), p.140427-140427, Article 140427

2020

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Discovery and Exploration of Protein Kinase CK2 Binding Sites Using CK2α′Cys336Ser as an Exquisite Crystallographic Tool

Kinases and Phosphatases, 2023-11, Vol.1 (4), p.306-322

2023

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Binding assay for characterization of protein kinase inhibitors possessing sub-picomolar to sub-millimolar affinity

Analytical biochemistry, 2017-08, Vol.531, p.67-77

2017

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Progesterone triggers Rho kinase-cofilin axis during in vitro and in vivo endometrial decidualization

Human reproduction (Oxford), 2021-08, Vol.36 (8), p.2230-2248

2021

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Unexpected CK2β-antagonistic functionality of bisubstrate inhibitors targeting protein kinase CK2

Bioorganic chemistry, 2020-03, Vol.96, p.103608-103608, Article 103608

2020

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High-affinity bisubstrate probe for fluorescence anisotropy binding/displacement assays with protein kinases PKA and ROCK

Analytical biochemistry, 2009-02, Vol.385 (1), p.85-93

2009

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Benzoselenadiazole-based responsive long-lifetime photoluminescent probes for protein kinases

Chemical communications (Cambridge, England), 2014-04, Vol.50 (31), p.4096-4098

2014

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FRET-based screening assay using small-molecule photoluminescent probes in lysate of cells overexpressing RFP-fused protein kinases

Analytical biochemistry, 2015-07, Vol.481, p.10-17

2015

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A subnanomolar fluorescent probe for protein kinase CK2 interaction studies

Organic & biomolecular chemistry, 2012-11, Vol.10 (43), p.8645-8653

2012

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Benzoselenadiazole-based responsive long-lifetime photoluminescent probes for protein kinasesElectronic supplementary information (ESI) available: Experimental details and further characterization. See DOI: 10.1039/c3cc49198f

2014-03

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Responsive microsecond-lifetime photoluminescent probes for analysis of protein kinases and their inhibitors

Biochimica et biophysica acta, 2013-07, Vol.1834 (7), p.1330-1335

2013

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Bisubstrate fluorescent probes and biosensors in binding assays for HTS of protein kinase inhibitors

Biochimica et biophysica acta, 2010-03, Vol.1804 (3), p.541-546

2010

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A subnanomolar fluorescent probe for protein kinase CK2 interaction studiesElectronic supplementary information (ESI) available: HPLC-MS data of synthesized compounds, selectivity table, X-ray diffraction data and copies of UV, 1H NMR and 13C NMR spectra of new compounds. See DOI: 10.1039/c2ob26022k

2012-11

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Surface-plasmon-resonance-based biosensor with immobilized bisubstrate analog inhibitor for the determination of affinities of ATP- and protein-competitive ligands of cAMP-dependent protein kinase

Analytical biochemistry, 2007-03, Vol.362 (2), p.268-277

2007

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Fluorometric TLC assay for evaluation of protein kinase inhibitors

Analytical biochemistry, 2005-05, Vol.340 (1), p.165-170

2005

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Liquid-phase synthesis of a pegylated adenosine–oligoarginine conjugate, cell-permeable inhibitor of cAMP-dependent protein kinase

Bioorganic & medicinal chemistry letters, 2003-09, Vol.13 (18), p.3035-3039

2003

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Liquid-phase synthesis of a pegylated adenosine-oligoarginine conjugate, cell-permeable inhibitor of cAMP-dependent protein kinase: Recent advances in the design of kinase inhibitors as novel therapeutic agents

Bioorganic & medicinal chemistry letters, 2003, Vol.13 (18), p.3035-3039

2003

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Amyloid precursor protein carboxy-terminal fragments modulate G-proteins and adenylate cyclase activity in Alzheimer’s disease brain

Brain research. Molecular brain research., 2003-09, Vol.117 (1), p.73-82

2003

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Protein Cargo Delivery Properties of Cell-Penetrating Peptides. A Comparative Study

Dissection of Protein Kinase Pathways in Live Cells Using Photoluminescent Probes: Surveillance or Interrogation?

Conjugation of Adenosine and Hexa-(d-arginine) Leads to a Nanomolar Bisubstrate-Analog Inhibitor of Basophilic Protein Kinases

Construction of Covalent Bisubstrate Inhibitor of Protein Kinase Reacting with Cysteine Residue at Substrate-Binding Site

Oligo-aspartic acid conjugates with benzo[c][2,6]naphthyridine-8-carboxylic acid scaffold as picomolar inhibitors of CK2

Thiazole- and selenazole-comprising high-affinity inhibitors possess bright microsecond-scale photoluminescence in complex with protein kinase CK2

Discovery of strong inhibitory properties of a monoclonal antibody of PKA and use of the antibody and a competitive photoluminescent orthosteric probe for analysis of the protein kinase

Discovery and Exploration of Protein Kinase CK2 Binding Sites Using CK2α′Cys336Ser as an Exquisite Crystallographic Tool

Binding assay for characterization of protein kinase inhibitors possessing sub-picomolar to sub-millimolar affinity

Progesterone triggers Rho kinase-cofilin axis during in vitro and in vivo endometrial decidualization

Unexpected CK2β-antagonistic functionality of bisubstrate inhibitors targeting protein kinase CK2

High-affinity bisubstrate probe for fluorescence anisotropy binding/displacement assays with protein kinases PKA and ROCK

Benzoselenadiazole-based responsive long-lifetime photoluminescent probes for protein kinases

FRET-based screening assay using small-molecule photoluminescent probes in lysate of cells overexpressing RFP-fused protein kinases

A subnanomolar fluorescent probe for protein kinase CK2 interaction studies

Benzoselenadiazole-based responsive long-lifetime photoluminescent probes for protein kinasesElectronic supplementary information (ESI) available: Experimental details and further characterization. See DOI: 10.1039/c3cc49198f

Responsive microsecond-lifetime photoluminescent probes for analysis of protein kinases and their inhibitors

Bisubstrate fluorescent probes and biosensors in binding assays for HTS of protein kinase inhibitors

A subnanomolar fluorescent probe for protein kinase CK2 interaction studiesElectronic supplementary information (ESI) available: HPLC-MS data of synthesized compounds, selectivity table, X-ray diffraction data and copies of UV, 1H NMR and 13C NMR spectra of new compounds. See DOI: 10.1039/c2ob26022k

Surface-plasmon-resonance-based biosensor with immobilized bisubstrate analog inhibitor for the determination of affinities of ATP- and protein-competitive ligands of cAMP-dependent protein kinase

Fluorometric TLC assay for evaluation of protein kinase inhibitors

Liquid-phase synthesis of a pegylated adenosine–oligoarginine conjugate, cell-permeable inhibitor of cAMP-dependent protein kinase

Liquid-phase synthesis of a pegylated adenosine-oligoarginine conjugate, cell-permeable inhibitor of cAMP-dependent protein kinase: Recent advances in the design of kinase inhibitors as novel therapeutic agents

Amyloid precursor protein carboxy-terminal fragments modulate G-proteins and adenylate cyclase activity in Alzheimer’s disease brain

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