Concepedia

Author

Uwe Trinks

Novartis (Switzerland)

Also Known As

U P Trinks, U Trinks, U. P. TRINKS, Uwe P. Trinks, Uwe TRINKS, Uwe Trinks

13

Publications

586

Citations

8

H-Index

23

Concepts

All Affiliations

Novartis (Switzerland)
UT

About

Uwe Trinks is an author at Novartis (Switzerland) specializing in medicine, pharmacology, and natural sciences.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

7

7

499

2

Natural Sciences

6

6

442

3

Biochemistry

5

5

365

4

Biomolecular Engineering

3

3

181

5

Engineering

1

1

73

Uwe Trinks

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8

Publications

572

Citations

8

H-Index

YearCitations

Modelling study of protein kinase inhibitors: Binding mode of staurosporine and origin of the selectivity of CGP 52411

Pascal Furet, Giorgio Caravatti, Nicholas Lydon,

Journal of Computer-Aided Molecular Design

1995

103

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.

Elisabeth Buchdunger, Uwe Trinks, Helmut Mett,

Proceedings of the National Academy of Sciences

1994

99

Dianilinophthalimides: Potent and Selective, ATP-Competitive Inhibitors of the EGF-Receptor Protein Tyrosine Kinase

Uwe Trinks, Elisabeth Buchdunger, Pascal Furet,

Journal of Medicinal Chemistry

1994

90

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

Peter Traxler, Uwe Trinks, Elisabeth Buchdunger,

Journal of Medicinal Chemistry

1995

77

Ethylene Biosynthesis part 10. Synthesis and study of racemic, (1<i>R</i>, 2<i>S</i>)‐, and (1<i>S</i>, 2<i>R</i>)‐1‐Amino‐2‐(hydroxymethyl)cyclopropanecarboxylic Acid

Michael C. Pirrung, S.E. Dunlap, Uwe Trinks

Helvetica Chimica Acta

1989

73

Inhibitory activity and selectivity of staurosporine derivatives towards protein kinase C

Giorgio Caravatti, Thomas Meyer, Andreas Fredenhagen,

Bioorganic & Medicinal Chemistry Letters

1994

58

Benzopyranones and benzothiopyranones: a class of tyrosine protein kinase inhibitors with selectivity for the v-abl kinase.

Johanna Geissler, Johannes Roesel, Thomas Meyer,

PubMed

1992

41

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

Elisabeth Buchdunger, Helmut Mett, Uwe Trinks,

PubMed

1995

31

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