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Genome-wide shRNA screen reveals increased mitochondrial dependence upon mTORC2 addiction

Oncogene, 2011-03, Vol.30 (13), p.1551-1565

2011

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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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A derivative of staurosporine (CGP 41 251) shows selectivity for protein kinase C inhibition and In vitro anti‐proliferative as well as In vivo anti‐tumor activity

International journal of cancer, 1989-05, Vol.43 (5), p.851-856

1989

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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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Thiazolidine-diones. Biochemical and biological activity of a novel class of tyrosine protein kinase inhibitors

The Journal of biological chemistry, 1990-12, Vol.265 (36), p.22255-22261

1990

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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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Indole alkaloids with in vitro antiproliferative activity from the ammoniacal extract of Nauclea orientalis

Planta medica, 1992-02, Vol.58 (1), p.43-48

1992

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Author errata

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

1999

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Differential inhibition of the epidermal growth factor-, platelet-derived growth factor-, and protein kinase C-mediated signal transduction pathways by the staurosporine derivative CGP 41251

Cancer research (Chicago, Ill.), 1992-10, Vol.52 (19), p.5353-5358

1992

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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

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RETRACTED: 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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[(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

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The protein kinase C inhibitor CGP 41251, a staurosporine derivative with antitumor activity, reverses multidrug resistance

International journal of cancer, 1994-04, Vol.57 (1), p.104-110

1994

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

Journal of medicinal chemistry, 1994-04, Vol.37 (7), p.1015-1027

1994

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Reversal of multidrug resistance by the staurosporine derivatives CGP 41251 and CGP 42700

International journal of cancer, 1998-07, Vol.77 (1), p.64-69

1998

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Involvement of protein kinase C in the growth regulation of human breast cancer cells

Cancer treatment and research, 1992, Vol.61, p.229

1992

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Stable Amplification of the S-Adenosylmethionine Decarboxylase Gene in Chinese Hamster Ovary Cells (∗)

The Journal of biological chemistry, 1995-02, Vol.270 (5), p.2124-2132

1995

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In vitro cultures of epithelial cells from healthy breast tissues and cells from breast carcinomas

Recent results in cancer research, 1989, Vol.113, p.4

1989

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S-Adenosylmethionine decarboxylase inhibitors: new aryl and heteroaryl analogs of methylglyoxal bis(guanylhydrazone)

Journal of medicinal chemistry, 1993, Vol.36 (1), p.46-54

1993

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4-Amidinoindan-1-one 2'-amidinohydrazone: a new potent and selective inhibitor of S-adenosylmethionine decarboxylase

Journal of medicinal chemistry, 1993-07, Vol.36 (15), p.2168-2171

1993

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Zur Systematik der grünen Grubenottern der Gattung Trimeresurus (Serpentes, Crotalidae)

Revue suisse de zoologie, 1981, Vol.88, p.163-205

1981

Volltextzugriff (PDF)

A derivative of staurosporine (CGP 41:251) shows selectivity for PKC inhibition and in vitro antiproliferative effects as well as in vivo antitumor activity. Int. J. Cancer, 43, 851–866 (1989)

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

1999

Volltextzugriff (PDF)

Author errata

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

1999

Volltextzugriff (PDF)

New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activity

Cancer research (Chicago, Ill.), 1992-09, Vol.52 (17), p.4712

1992

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3.27 Optical Assays in Drug Discovery

Comprehensive Medicinal Chemistry II, 2007, Vol.3, p.577-598

2007

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Genome-wide shRNA screen reveals increased mitochondrial dependence upon mTORC2 addiction

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

A derivative of staurosporine (CGP 41 251) shows selectivity for protein kinase C inhibition and In vitro anti‐proliferative as well as In vivo anti‐tumor activity

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

Thiazolidine-diones. Biochemical and biological activity of a novel class of tyrosine protein kinase inhibitors

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

Indole alkaloids with in vitro antiproliferative activity from the ammoniacal extract of Nauclea orientalis

Author errata

Differential inhibition of the epidermal growth factor-, platelet-derived growth factor-, and protein kinase C-mediated signal transduction pathways by the staurosporine derivative CGP 41251

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

RETRACTED: Selective inhibition of the platelet-derived growth factor signal transduction pathway by a protein-tyrosine kinase inhibitor of the 2-phenylaminopyrimidine class

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

The protein kinase C inhibitor CGP 41251, a staurosporine derivative with antitumor activity, reverses multidrug resistance

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

Reversal of multidrug resistance by the staurosporine derivatives CGP 41251 and CGP 42700

Involvement of protein kinase C in the growth regulation of human breast cancer cells

Stable Amplification of the S-Adenosylmethionine Decarboxylase Gene in Chinese Hamster Ovary Cells (∗)

In vitro cultures of epithelial cells from healthy breast tissues and cells from breast carcinomas

S-Adenosylmethionine decarboxylase inhibitors: new aryl and heteroaryl analogs of methylglyoxal bis(guanylhydrazone)

4-Amidinoindan-1-one 2'-amidinohydrazone: a new potent and selective inhibitor of S-adenosylmethionine decarboxylase

Zur Systematik der grünen Grubenottern der Gattung Trimeresurus (Serpentes, Crotalidae)

A derivative of staurosporine (CGP 41:251) shows selectivity for PKC inhibition and in vitro antiproliferative effects as well as in vivo antitumor activity. Int. J. Cancer, 43, 851–866 (1989)

Author errata

New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activity

3.27 Optical Assays in Drug Discovery

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