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Helmut Mett

Novartis

75

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4708

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Phenylamino-Pyrimidine (PAP)-Derivatives: A New Class of Potent and Highly Selective PDGF-Receptor Autophosphorylation Inhibitors.

2010 ChemInform
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2,6,9-Trisubstituted Purines: Optimization Towards Highly Potent and Selective CDK1 Inhibitors.

2010 ChemInform
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Substituted 5,7-Diphenyl-pyrrolo[2,3-d]pyrimidines: Potent Inhibitors of the Tyrosine Kinase c-Src.

2010 ChemInform
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Semicochliodinol A and B: Inhibitors of HIV-1 Protease and EGF-R Protein Tyrosine Kinase Related to Asterriquinones Produced by the Fungus Chrysosporium merdarium.

2010 ChemInform
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New Cationic Lipids Form Channel-Like Pores in Phospholipid Bilayers

2003 Biophysical Journal
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Substituted 5,7-diphenyl-pyrrolo[2,3d]pyrimidines: potent inhibitors of the tyrosine kinase c-Src.

2000 Bioorganic & Medicinal Chemistry Letters
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Corrigendum to “2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitors”

2000 Bioorganic & Medicinal Chemistry Letters
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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.

2000 Cancer Research
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Use of a Pharmacophore Model for the Design of EGFR Tyrosine Kinase Inhibitors: Isoflavones and 3-Phenyl-4(1H)-quinolones

1999 Journal of Medicinal Chemistry
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Inhibitors of Protein Kinases

1999 Pharmacology & Therapeutics
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