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Selective Inhibition of the Platelet-Derived Growth Factor Signal Transduction Pathway by a Protein-Tyrosine Kinase Inhibitor of the 2- Phenylaminopyrimidine Class

Proceedings of the National Academy of Sciences - PNAS, 1995-03, Vol.92 (7), p.2558-2562

1995

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Alterations in ornithine decarboxylase characteristics account for tolerance of Trypanosoma brucei rhodesiense to D,L-alpha-difluoromethylornithine

Antimicrobial Agents and Chemotherapy, 1997-09, Vol.41 (9), p.1922-1925

1997

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PTK787/ZK 222584, a novel and potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, impairs vascular endothelial growth factor-induced responses and tumor growth after oral administration

Cancer research (Chicago, Ill.), 2000-04, Vol.60 (8), p.2178-2189

2000

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4,5-Dianilinophthalimide: A Protein-Tyrosine Kinase Inhibitor with Selectivity for the Epidermal Growth Factor Receptor Signal Transduction Pathway and Potent in vivo Antitumor Activity

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (6), p.2334-2338

1994

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Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative

Cancer research (Chicago, Ill.), 1996, Vol.56 (1), p.100-104

1996

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Use of a Pharmacophore Model for the Design of EGF-R Tyrosine Kinase Inhibitors: 4-(Phenylamino)pyrazolo[3,4-d]pyrimidines

Journal of medicinal chemistry, 1997-10, Vol.40 (22), p.3601-3616

1997

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In vitro trypanocidal activities of new S-adenosylmethionine decarboxylase inhibitors

Antimicrobial Agents and Chemotherapy, 1996-06, Vol.40 (6), p.1442-1447

1996

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Potent and selective inhibitors of the Abl-kinase: phenylamino-pyrimidine (PAP) derivatives

Bioorganic & medicinal chemistry letters, 1997-01, Vol.7 (2), p.187-192

1997

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Inhibitors of Protein Kinases: CGP 41251, a Protein Kinase Inhibitor with Potential as an Anticancer Agent

Pharmacology & therapeutics (Oxford), 1999-05, Vol.82 (2), p.293-301

1999

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Use of a Pharmacophore Model for the Design of EGFR Tyrosine Kinase Inhibitors: Isoflavones and 3-Phenyl-4(1H)-quinolones

Journal of medicinal chemistry, 1999-03, Vol.42 (6), p.1018-1026

1999

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4,5-bis(4-fluoroanilino)phthalimide: A selective inhibitor of the epidermal growth factor receptor signal transduction pathway with potent in vivo antitumor activity

Clinical cancer research, 1995-08, Vol.1 (8), p.813-821

1995

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The Target of Penicillin: The Murein Sacculus of Bacterial Cell Walls Architecture and Growth. Proceedings International FEMS Symposium Berlin (West), Germany, March 13-18, 1983

1, 2019

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4-(Phenylamino)pyrrolopyrimidines: Potent and Selective, ATP Site Directed Inhibitors of the EGF-Receptor Protein Tyrosine Kinase

Journal of medicinal chemistry, 1996-06, Vol.39 (12), p.2285-2292

1996

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2,6,9-trisubstituted purines : Optimization towards highly potent and selective CDK1 inhibitors

Bioorganic & medicinal chemistry letters, 1999-01, Vol.9 (1), p.91-96

1999

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Phenylamino-pyrimidine (PAP) — derivatives: a new class of potent and highly selective PDGF-receptor autophosphorylation inhibitors

Bioorganic & medicinal chemistry letters, 1996-06, Vol.6 (11), p.1221-1226

1996

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Physiological studies of the regulation of beta-lactamase expression in Pseudomonas maltophilia

Journal of Bacteriology, 1989-01, Vol.171 (1), p.483-487

1989

Volltextzugriff (PDF)

Author errata

International journal of cancer, 1999-05, Vol.81 (4), p.669-669

1999

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EFFECT OF DRUGS ON THE FORMATION AND STRUCTURE OF INTERMEDIATES OF ESCHERICHIA COLI MUREIN BIOSYNTHESIS

The Target of Penicillin, 2019, p.565-570

Originally published 1983, 2019

Volltextzugriff (PDF)

CGP 48664, a new S-adenosylmethionine decarboxylase inhibitor with broad spectrum antiproliferative and antitumor activity

Cancer research (Chicago, Ill.), 1994-06, Vol.54 (12), p.3210-3217

1994

Volltextzugriff (PDF)

Substituted 5,7-diphenyl-pyrrolo[2,3d]pyrimidines: potent inhibitors of the tyrosine kinase c-Src

Bioorganic & medicinal chemistry letters, 2000-05, Vol.10 (9), p.945-949

2000

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Development of solid-phase enzyme-linked immunosorbent assays for the determination of epidermal growth factor receptor and pp60c-src tyrosine protein kinase activity

Analytical biochemistry, 1992-05, Vol.203 (1), p.151-157

1992

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[(Alkylamino)methyl]acrylophenones: Potent and Selective Inhibitors of the Epidermal Growth Factor Receptor Protein Tyrosine Kinase

Journal of medicinal chemistry, 1995-06, Vol.38 (13), p.2441-2448

1995

Volltextzugriff (PDF)

New Cationic Lipids Form Channel-Like Pores in Phospholipid Bilayers

Biophysical journal, 2003-03, Vol.84 (3), p.1750-1755

2003

Volltextzugriff (PDF)

Effects of low concentrations of antibiotics on Escherichia coli adhesion

Antimicrobial Agents and Chemotherapy, 1982-06, Vol.21 (6), p.864-869

1982

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Duodeno-pancreatic secretions enhance bactericidal activity of antimicrobial drugs

Antimicrobial Agents and Chemotherapy, 1984-07, Vol.26 (1), p.35-38

1984

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Selective Inhibition of the Platelet-Derived Growth Factor Signal Transduction Pathway by a Protein-Tyrosine Kinase Inhibitor of the 2- Phenylaminopyrimidine Class

Alterations in ornithine decarboxylase characteristics account for tolerance of Trypanosoma brucei rhodesiense to D,L-alpha-difluoromethylornithine

PTK787/ZK 222584, a novel and potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, impairs vascular endothelial growth factor-induced responses and tumor growth after oral administration

4,5-Dianilinophthalimide: A Protein-Tyrosine Kinase Inhibitor with Selectivity for the Epidermal Growth Factor Receptor Signal Transduction Pathway and Potent in vivo Antitumor Activity

Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative

Use of a Pharmacophore Model for the Design of EGF-R Tyrosine Kinase Inhibitors: 4-(Phenylamino)pyrazolo[3,4-d]pyrimidines

In vitro trypanocidal activities of new S-adenosylmethionine decarboxylase inhibitors

Potent and selective inhibitors of the Abl-kinase: phenylamino-pyrimidine (PAP) derivatives

Inhibitors of Protein Kinases: CGP 41251, a Protein Kinase Inhibitor with Potential as an Anticancer Agent

Use of a Pharmacophore Model for the Design of EGFR Tyrosine Kinase Inhibitors: Isoflavones and 3-Phenyl-4(1H)-quinolones

4,5-bis(4-fluoroanilino)phthalimide: A selective inhibitor of the epidermal growth factor receptor signal transduction pathway with potent in vivo antitumor activity

The Target of Penicillin: The Murein Sacculus of Bacterial Cell Walls Architecture and Growth. Proceedings International FEMS Symposium Berlin (West), Germany, March 13-18, 1983

4-(Phenylamino)pyrrolopyrimidines: Potent and Selective, ATP Site Directed Inhibitors of the EGF-Receptor Protein Tyrosine Kinase

2,6,9-trisubstituted purines : Optimization towards highly potent and selective CDK1 inhibitors

Phenylamino-pyrimidine (PAP) — derivatives: a new class of potent and highly selective PDGF-receptor autophosphorylation inhibitors

Physiological studies of the regulation of beta-lactamase expression in Pseudomonas maltophilia

Author errata

EFFECT OF DRUGS ON THE FORMATION AND STRUCTURE OF INTERMEDIATES OF ESCHERICHIA COLI MUREIN BIOSYNTHESIS

CGP 48664, a new S-adenosylmethionine decarboxylase inhibitor with broad spectrum antiproliferative and antitumor activity

Substituted 5,7-diphenyl-pyrrolo[2,3d]pyrimidines: potent inhibitors of the tyrosine kinase c-Src

Development of solid-phase enzyme-linked immunosorbent assays for the determination of epidermal growth factor receptor and pp60c-src tyrosine protein kinase activity

[(Alkylamino)methyl]acrylophenones: Potent and Selective Inhibitors of the Epidermal Growth Factor Receptor Protein Tyrosine Kinase

New Cationic Lipids Form Channel-Like Pores in Phospholipid Bilayers

Effects of low concentrations of antibiotics on Escherichia coli adhesion

Duodeno-pancreatic secretions enhance bactericidal activity of antimicrobial drugs

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