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Caffeic Acid Phenethyl Ester is a Potent and Specific Inhibitor of Activation of Nuclear Transcription Factor NF-κ B

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (17), p.9090-9095

1996

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Yersinia pestis and approaches to targeting its outer protein H protein-tyrosine phosphatase (YopH)

Current medicinal chemistry, 2012-11, Vol.19 (33), p.5726-5734

2012

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Coumarin-Based Inhibitors of HIV Integrase

Journal of medicinal chemistry, 1997-01, Vol.40 (2), p.242-249

1997

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Chicoric Acid Analogues as HIV-1 Integrase Inhibitors

Journal of medicinal chemistry, 1999-04, Vol.42 (8), p.1401-1414

1999

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Synergistic anti-leukemic activity of imatinib in combination with a small molecule Grb2 SH2 domain binding antagonist

Leukemia, 2014-04, Vol.28 (4), p.948-951

2014

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Hydroxylated Aromatic Inhibitors of HIV-1 Integrase

Journal of medicinal chemistry, 1995-10, Vol.38 (21), p.4171-4178

1995

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Application of OCT-angiography to characterise the evolution of chorioretinal lesions in acute posterior multifocal placoid pigment epitheliopathy

Eye (London), 2017-10, Vol.31 (10), p.1399-1408

2017

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Diarylsulfones, a novel class of human immunodeficiency virus type 1 integrase inhibitors

Antimicrobial Agents and Chemotherapy, 1997-02, Vol.41 (2), p.385-393

1997

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Potent Blockade of Hepatocyte Growth Factor-stimulated Cell Motility, Matrix Invasion and Branching Morphogenesis by Antagonists of Grb2 Src Homology 2 Domain Interactions

The Journal of biological chemistry, 2001-04, Vol.276 (17), p.14308-14314

2001

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Syp (SH-PTP2) is a positive mediator of growth factor-stimulated mitogenic signal transduction

The Journal of biological chemistry, 1994-08, Vol.269 (33), p.21244-21248

1994

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Antiretroviral Agents as Inhibitors of both Human Immunodeficiency Virus Type 1 Integrase and Protease

Journal of medicinal chemistry, 1996-06, Vol.39 (13), p.2472-2481

1996

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Hydrazide-Containing Inhibitors of HIV-1 Integrase

Journal of medicinal chemistry, 1997-03, Vol.40 (6), p.937-941

1997

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Arylamide Inhibitors of HIV-1 Integrase

Journal of medicinal chemistry, 1997-04, Vol.40 (8), p.1186-1194

1997

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Discovery of HIV-1 Integrase Inhibitors by Pharmacophore Searching

Journal of medicinal chemistry, 1997-03, Vol.40 (6), p.930-936

1997

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CX-4945, a selective inhibitor of casein kinase-2 (CK2), exhibits anti-tumor activity in hematologic malignancies including enhanced activity in chronic lymphocytic leukemia when combined with fludarabine and inhibitors of the B-cell receptor pathway

Leukemia, 2013-10, Vol.27 (10), p.2094-2096

2013

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Potent Inhibition of Grb2 SH2 Domain Binding by Non-Phosphate-Containing Ligands

Journal of medicinal chemistry, 1999-01, Vol.42 (1), p.25-35

1999

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Salicylhydrazine-Containing Inhibitors of HIV-1 Integrase: Implication for a Selective Chelation in the Integrase Active Site

Journal of medicinal chemistry, 1998-08, Vol.41 (17), p.3202-3209

1998

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HIV-1 Integrase and Virus and Cell DNAs: Complex Formation and Perturbation by Inhibitors of Integration

Neurochemical research, 2010-06, Vol.35 (6), p.888-893

2010

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Inhibition of Grb2 SH2 Domain Binding by Non-Phosphate-Containing Ligands. 2. 4-(2-Malonyl)phenylalanine as a Potent Phosphotyrosyl Mimetic

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.911-920

2000

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Structure of the Catalytic Domain of Avian Sarcoma Virus Integrase with a Bound HIV-1 Integrase-Targeted Inhibitor

Proceedings of the National Academy of Sciences - PNAS, 1998-04, Vol.95 (9), p.4831-4836

1998

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Protein-tyrosine phosphatases: Structure, mechanism, and inhibitor discovery

BIOPOLYM, 1998, Vol.47 (3), p.225-241

1998

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Viral Entry as the Primary Target for the Anti-HIV Activity of Chicoric Acid and Its Tetra-Acetyl Esters

Molecular pharmacology, 2000-09, Vol.58 (3), p.641-648

2000

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4‘-O-[2-(2-Fluoromalonyl)]-l-tyrosine: A Phosphotyrosyl Mimic for the Preparation of Signal Transduction Inhibitory Peptides

Journal of medicinal chemistry, 1996-03, Vol.39 (5), p.1021-1027

1996

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Phosphonate inhibitors of protein-tyrosine and serine/threonine phosphatases

Biochemical journal, 1995-11, Vol.311 ( Pt 3) (3), p.1025-1031

1995

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Structural Basis for Inhibition of the Protein Tyrosine Phosphatase 1B by Phosphotyrosine Peptide Mimetics

Biochemistry (Easton), 1998-12, Vol.37 (51), p.17773-17783

1998

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Caffeic Acid Phenethyl Ester is a Potent and Specific Inhibitor of Activation of Nuclear Transcription Factor NF-κ B

Yersinia pestis and approaches to targeting its outer protein H protein-tyrosine phosphatase (YopH)

Coumarin-Based Inhibitors of HIV Integrase

Chicoric Acid Analogues as HIV-1 Integrase Inhibitors

Synergistic anti-leukemic activity of imatinib in combination with a small molecule Grb2 SH2 domain binding antagonist

Hydroxylated Aromatic Inhibitors of HIV-1 Integrase

Application of OCT-angiography to characterise the evolution of chorioretinal lesions in acute posterior multifocal placoid pigment epitheliopathy

Diarylsulfones, a novel class of human immunodeficiency virus type 1 integrase inhibitors

Potent Blockade of Hepatocyte Growth Factor-stimulated Cell Motility, Matrix Invasion and Branching Morphogenesis by Antagonists of Grb2 Src Homology 2 Domain Interactions

Syp (SH-PTP2) is a positive mediator of growth factor-stimulated mitogenic signal transduction

Antiretroviral Agents as Inhibitors of both Human Immunodeficiency Virus Type 1 Integrase and Protease

Hydrazide-Containing Inhibitors of HIV-1 Integrase

Arylamide Inhibitors of HIV-1 Integrase

Discovery of HIV-1 Integrase Inhibitors by Pharmacophore Searching

CX-4945, a selective inhibitor of casein kinase-2 (CK2), exhibits anti-tumor activity in hematologic malignancies including enhanced activity in chronic lymphocytic leukemia when combined with fludarabine and inhibitors of the B-cell receptor pathway

Potent Inhibition of Grb2 SH2 Domain Binding by Non-Phosphate-Containing Ligands

Salicylhydrazine-Containing Inhibitors of HIV-1 Integrase: Implication for a Selective Chelation in the Integrase Active Site

HIV-1 Integrase and Virus and Cell DNAs: Complex Formation and Perturbation by Inhibitors of Integration

Inhibition of Grb2 SH2 Domain Binding by Non-Phosphate-Containing Ligands. 2. 4-(2-Malonyl)phenylalanine as a Potent Phosphotyrosyl Mimetic

Structure of the Catalytic Domain of Avian Sarcoma Virus Integrase with a Bound HIV-1 Integrase-Targeted Inhibitor

Protein-tyrosine phosphatases: Structure, mechanism, and inhibitor discovery

Viral Entry as the Primary Target for the Anti-HIV Activity of Chicoric Acid and Its Tetra-Acetyl Esters

4‘-O-[2-(2-Fluoromalonyl)]-l-tyrosine: A Phosphotyrosyl Mimic for the Preparation of Signal Transduction Inhibitory Peptides

Phosphonate inhibitors of protein-tyrosine and serine/threonine phosphatases

Structural Basis for Inhibition of the Protein Tyrosine Phosphatase 1B by Phosphotyrosine Peptide Mimetics

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