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The knowledge modeling for chronic urticaria assessment in clinical decision support system with PDA

AMIA ... Annual Symposium proceedings, 2003, Vol.2003, p.902-902

2003

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Nanoformulated Single‐Stranded RNA‐Based Adjuvant with a Coordinative Amphiphile as an Effective Stabilizer: Inducing Humoral Immune Response by Activation of Antigen‐Presenting Cells

Angewandte Chemie International Edition, 2020-07, Vol.59 (28), p.11540-11549

International ed. in English, 2020

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Discovery of New Quinolone-Based Diarylamides as Potent B-RAFV600E/C-RAF Kinase Inhibitors Endowed with Promising In Vitro Anticancer Activity

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3216

2023

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Discovery of new 6-ureido/amidocoumarins as highly potent and selective inhibitors for the tumour-relevant carbonic anhydrases IX and XII

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2154603-2154603

2023

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Overcoming the imatinib-resistant BCR-ABL mutants with new ureidobenzothiazole chemotypes endowed with potent and broad-spectrum anticancer activity

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2189097-2189097

2023

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Identification of New N -methyl-piperazine Chalcones as Dual MAO-B/AChE Inhibitors

Pharmaceuticals (Basel, Switzerland), 2023-01, Vol.16 (1), p.83

2023

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Discovery of New Quinoline-Based Diarylamides as Potent B-RAFV600E/C-RAF Kinase Inhibitors Endowed with Promising In Vitro Anticancer Activity

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3216

2023

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Discovery of 3-((3-amino-1H-indazol-4-yl)ethynyl)-N-(4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide (AKE-72), a potent Pan-BCR-ABL inhibitor including the T315I gatekeeper resistant mutant

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2228515-2228515

2023

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Discovery and development of heat shock protein 90 inhibitors as anticancer agents: a review of patented potent geldanamycin derivatives

Expert opinion on therapeutic patents, 2013-08, Vol.23 (8), p.919-943

2013

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Structure-activity relationship (SAR) studies on the mutagenic properties of 2,7-diaminofluorene and 2,7-diaminocarbazole derivatives

Bioorganic & medicinal chemistry letters, 2021-01, Vol.31, p.127662, Article 127662

2021

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Coordinative Amphiphiles as Tunable siRNA Transporters

Bioconjugate chemistry, 2016-08, Vol.27 (8), p.1850-1856

2016

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Synthesis and T-type calcium channel-blocking effects of aryl(1,5-disubstituted-pyrazol-3-yl)methyl sulfonamides for neuropathic pain treatment

European journal of medicinal chemistry, 2016-11, Vol.123, p.665-672

2016

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Sulfur(vi) fluoride exchange as a key reaction for synthesizing biaryl sulfate core derivatives as potent hepatitis C virus NS5A inhibitors and their structure-activity relationship studies

RSC advances, 2018-01, Vol.8 (55), p.31803-31821

2018

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Structural Basis for Design of New Purine-Based Inhibitors Targeting the Hydrophobic Binding Pocket of Hsp90

International journal of molecular sciences, 2020-12, Vol.21 (24), p.9377

2020

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Discovery of G Protein-Biased Antagonists against 5‑HT7R

Journal of medicinal chemistry, 2021-09, Vol.64 (18), p.13766-13779

2021

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Identification of Ureidocoumarin-Based Selective Discoidin Domain Receptor 1 (DDR1) Inhibitors via Drug Repurposing Approach, Biological Evaluation, and In Silico Studies

Pharmaceuticals (Basel, Switzerland), 2024-03, Vol.17 (4), p.427

2024

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Design and Synthesis of New 4-(3,4,5-Trimethoxyphenyl)Thiazole-Pyrimidine Derivatives as Potential Antiproliferative Agents

Medicina (Kaunas, Lithuania), 2023-06, Vol.59 (6), p.1076

2023

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Discovery of G Protein-Biased Antagonists against 5-HT 7 R

Journal of medicinal chemistry, 2021-09, Vol.64 (18), p.13766-13779

2021

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Discovery of thiophen-2-ylmethylene bis-dimedone derivatives as novel WRN inhibitors for treating cancers with microsatellite instability

Bioorganic & medicinal chemistry, 2024-02, Vol.100, p.117588-117588, Article 117588

2024

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Synthesis and in Vitro Evaluation of the Antitubercular and Antibacterial Activity of Novel Oxazolidinones Bearing Octahydrocyclopenta[c]pyrrol-2-yl Moieties

Chemical and Pharmaceutical Bulletin, 2014/12/01, Vol.62(12), pp.1214-1224

2014

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Analyzing immune responses to varied mRNA and protein vaccine sequences

npj vaccines, 2023-06, Vol.8 (1), p.84-84, Article 84

2023

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A novel tropomyosin-related kinase A inhibitor, KK5101 to treat pancreatic cancer

Cancer letters, 2018-07, Vol.426, p.25-36

2018

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Novel coumarin benzamides as potent and reversible monoamine oxidase-B inhibitors: Design, synthesis, and neuroprotective effects

Bioorganic chemistry, 2024-01, Vol.142, p.106939, Article 106939

2024

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Analysis of the Immunostimulatory Effects of Cytokine-Expressing Internal Ribosome Entry Site-Based RNA Adjuvants and Their Applications

The Journal of infectious diseases, 2024-05, Vol.229 (5), p.1408-1418

2024

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The knowledge modeling for chronic urticaria assessment in clinical decision support system with PDA

Nanoformulated Single‐Stranded RNA‐Based Adjuvant with a Coordinative Amphiphile as an Effective Stabilizer: Inducing Humoral Immune Response by Activation of Antigen‐Presenting Cells

mRNA‐HPV vaccine encoding E6 and E7 improves therapeutic potential for HPV‐mediated cancers via subcutaneous immunization

Discovery of New Quinolone-Based Diarylamides as Potent B-RAFV600E/C-RAF Kinase Inhibitors Endowed with Promising In Vitro Anticancer Activity

Discovery of new 6-ureido/amidocoumarins as highly potent and selective inhibitors for the tumour-relevant carbonic anhydrases IX and XII

Overcoming the imatinib-resistant BCR-ABL mutants with new ureidobenzothiazole chemotypes endowed with potent and broad-spectrum anticancer activity

Identification of New N -methyl-piperazine Chalcones as Dual MAO-B/AChE Inhibitors

Discovery of New Quinoline-Based Diarylamides as Potent B-RAFV600E/C-RAF Kinase Inhibitors Endowed with Promising In Vitro Anticancer Activity

Discovery of 3-((3-amino-1H-indazol-4-yl)ethynyl)-N-(4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide (AKE-72), a potent Pan-BCR-ABL inhibitor including the T315I gatekeeper resistant mutant

Discovery and development of heat shock protein 90 inhibitors as anticancer agents: a review of patented potent geldanamycin derivatives

Structure-activity relationship (SAR) studies on the mutagenic properties of 2,7-diaminofluorene and 2,7-diaminocarbazole derivatives

Coordinative Amphiphiles as Tunable siRNA Transporters

Synthesis and T-type calcium channel-blocking effects of aryl(1,5-disubstituted-pyrazol-3-yl)methyl sulfonamides for neuropathic pain treatment

Sulfur(vi) fluoride exchange as a key reaction for synthesizing biaryl sulfate core derivatives as potent hepatitis C virus NS5A inhibitors and their structure-activity relationship studies

Structural Basis for Design of New Purine-Based Inhibitors Targeting the Hydrophobic Binding Pocket of Hsp90

Discovery of G Protein-Biased Antagonists against 5‑HT7R

Identification of Ureidocoumarin-Based Selective Discoidin Domain Receptor 1 (DDR1) Inhibitors via Drug Repurposing Approach, Biological Evaluation, and In Silico Studies

Design and Synthesis of New 4-(3,4,5-Trimethoxyphenyl)Thiazole-Pyrimidine Derivatives as Potential Antiproliferative Agents

Discovery of G Protein-Biased Antagonists against 5-HT 7 R

Discovery of thiophen-2-ylmethylene bis-dimedone derivatives as novel WRN inhibitors for treating cancers with microsatellite instability

Synthesis and in Vitro Evaluation of the Antitubercular and Antibacterial Activity of Novel Oxazolidinones Bearing Octahydrocyclopenta[c]pyrrol-2-yl Moieties

Analyzing immune responses to varied mRNA and protein vaccine sequences

A novel tropomyosin-related kinase A inhibitor, KK5101 to treat pancreatic cancer

Novel coumarin benzamides as potent and reversible monoamine oxidase-B inhibitors: Design, synthesis, and neuroprotective effects

Analysis of the Immunostimulatory Effects of Cytokine-Expressing Internal Ribosome Entry Site-Based RNA Adjuvants and Their Applications

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