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Structural insights into the inhibition of cytosolic 5'-nucleotidase II (cN-II) by ribonucleoside 5'-monophosphate analogues

PLoS computational biology, 2011-12, Vol.7 (12), p.e1002295-e1002295

2011

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From a Natural Product Lead to the Identification of Potent and Selective Benzofuran-3-yl-(indol-3-yl)maleimides as Glycogen Synthase Kinase 3β Inhibitors That Suppress Proliferation and Survival of Pancreatic Cancer Cells

Journal of medicinal chemistry, 2009-04, Vol.52 (7), p.1853-1863

2009

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Glycogen synthase kinase 3β inhibitors induce apoptosis in ovarian cancer cells and inhibit in-vivo tumor growth

Anti-cancer drugs, 2011-11, Vol.22 (10), p.978-985

2011

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Ex-Chiral-Pool Synthesis of β-Hydroxyphosphonate Nucleoside Analogues

European Journal of Organic Chemistry, 2007-02, Vol.2007 (6), p.925-933

2007

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Developing an efficient route to the synthesis of nucleoside 1-alkynylphosphonates

Tetrahedron, 2009-08, Vol.65 (31), p.6039-6046

2009

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Developing an efficient route to the synthesis of nucleoside 1-alkylnylphosphonates

Tetrahedron, 2009, Vol.65, p.6039-6046

2009

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Novel Glycogen Synthase Kinase 3beta Inhibitors Induce Apoptosis in Ovarian Cancer

Biology of reproduction, 2010-11, Vol.83 (Suppl_1), p.691-691

2010

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Structural Insights into the Inhibition of Cytosolic 5'-Nucleotidase II (cN-II) by Ribonucleoside 5'-Monophosphate Analogues: e1002295

PLoS computational biology, 2011-12, Vol.7 (12)

2011

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Use of microwave irradiation for sugar and nucleoside phosphonates synthesis

Tetrahedron letters, 2006-10, Vol.47 (44), p.7719-7721

2006

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5′,6′-Nucleoside Phosphonate Analogues Architecture: Synthesis and Comparative Evaluation towards Metabolic Enzymes

ChemMedChem, 2011-06, Vol.6 (6), p.1094-1106

2011

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Use of molecular modeling, docking, and 3D-QSAR studies for the determination of the binding mode of benzofuran-3-yl-(indol-3-yl)maleimides as GSK-3β inhibitors

Journal of molecular modeling, 2009-12, Vol.15 (12), p.1463-1479

2009

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Use of Molecular Modelling, Docking, and 3D-QSAR Studies for the Determination of the Binding Mode of 3-Benzofuranyl-4-indolyl-maleimides as GSK-3β Inhibitors

Journal of molecular modeling, 2009-05, Vol.15 (12), p.1463-1479

2009

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Improvement of the Synthesis of Sugar Phosphonates Using Microwave Irradiations

Nucleosides, nucleotides & nucleic acids, 2007-01, Vol.26 (10-12), p.1513-1515

2007

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Use of molecular modeling, docking, and 3D-QSAR studies for the determination of the binding mode of benzofuran-3-yl-(indol-3-yl)maleimides as GSK-3beta inhibitors

Journal of molecular modeling, 2009-12, Vol.15 (12), p.1463-1479

2009

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From a natural product lead to the identification of potent and selective benzofuran-3-yl-(indol-3-yl)maleimides as glycogen synthase kinase 3beta inhibitors that suppress proliferation and survival of pancreatic cancer cells

Journal of medicinal chemistry, 2009-04, Vol.52 (7), p.1853-1863

2009

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ChemInform Abstract: Developing an Efficient Route to the Synthesis of Nucleoside 1-Alkynylphosphonates

ChemInform, 2009-11, Vol.40 (47), p.no-no

2009

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Use of Microwave Irradiation for Sugar and Nucleoside Phosphonates Synthesis

ChemInform, 2007-02, Vol.38 (7), p.no-no

2007

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The role of thermophoresis on aluminum oxide lobe formation

Combustion and flame, 2021-06, Vol.228, p.142-153

2021

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Aluminum Combustion Driven Instabilities in Solid Rocket Motors

Journal of propulsion and power, 2009-03, Vol.25 (2), p.509-521

2009

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Synthesis and antitumor activities investigation of a C-nucleoside analogue of ribavirin

European journal of medicinal chemistry, 2020-02, Vol.188, p.112009, Article 112009

2020

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Studies of membranotropic and fusogenic activity of two putative HCV fusion peptides

Biochimica et biophysica acta. Biomembranes, 2019-01, Vol.1861 (1), p.50-61

2019

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Structural insights into the inhibition of cytosolic 5'-nucleotidase II (cN-II) by ribonucleoside 5'-monophosphate analogues

From a Natural Product Lead to the Identification of Potent and Selective Benzofuran-3-yl-(indol-3-yl)maleimides as Glycogen Synthase Kinase 3β Inhibitors That Suppress Proliferation and Survival of Pancreatic Cancer Cells

Glycogen synthase kinase 3β inhibitors induce apoptosis in ovarian cancer cells and inhibit in-vivo tumor growth

Ex-Chiral-Pool Synthesis of β-Hydroxyphosphonate Nucleoside Analogues

Developing an efficient route to the synthesis of nucleoside 1-alkynylphosphonates

Developing an efficient route to the synthesis of nucleoside 1-alkylnylphosphonates

Novel Glycogen Synthase Kinase 3beta Inhibitors Induce Apoptosis in Ovarian Cancer

Structural Insights into the Inhibition of Cytosolic 5'-Nucleotidase II (cN-II) by Ribonucleoside 5'-Monophosphate Analogues: e1002295

Use of microwave irradiation for sugar and nucleoside phosphonates synthesis

5′,6′-Nucleoside Phosphonate Analogues Architecture: Synthesis and Comparative Evaluation towards Metabolic Enzymes

Use of molecular modeling, docking, and 3D-QSAR studies for the determination of the binding mode of benzofuran-3-yl-(indol-3-yl)maleimides as GSK-3β inhibitors

Use of Molecular Modelling, Docking, and 3D-QSAR Studies for the Determination of the Binding Mode of 3-Benzofuranyl-4-indolyl-maleimides as GSK-3β Inhibitors

Improvement of the Synthesis of Sugar Phosphonates Using Microwave Irradiations

Use of molecular modeling, docking, and 3D-QSAR studies for the determination of the binding mode of benzofuran-3-yl-(indol-3-yl)maleimides as GSK-3beta inhibitors

From a natural product lead to the identification of potent and selective benzofuran-3-yl-(indol-3-yl)maleimides as glycogen synthase kinase 3beta inhibitors that suppress proliferation and survival of pancreatic cancer cells

ChemInform Abstract: Developing an Efficient Route to the Synthesis of Nucleoside 1-Alkynylphosphonates

Use of Microwave Irradiation for Sugar and Nucleoside Phosphonates Synthesis

The role of thermophoresis on aluminum oxide lobe formation

Aluminum Combustion Driven Instabilities in Solid Rocket Motors

Synthesis and antitumor activities investigation of a C-nucleoside analogue of ribavirin

Studies of membranotropic and fusogenic activity of two putative HCV fusion peptides

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