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Imidazopyrimidines, potent inhibitors of p38 MAP kinase

Bioorganic & medicinal chemistry letters, 2003-02, Vol.13 (3), p.347-350

2003

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Benzazepinones and Benzoxazepinones as Antagonists of Inhibitor of Apoptosis Proteins (IAPs) Selective for the Second Baculovirus IAP Repeat (BIR2) Domain

Journal of medicinal chemistry, 2013-10, Vol.56 (20), p.7772-7787

2013

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In Vivo Characterization of a Dual Adenosine A2A/A1 Receptor Antagonist in Animal Models of Parkinson’s Disease

Journal of medicinal chemistry, 2010-11, Vol.53 (22), p.8104-8115

2010

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Optimization of Benzodiazepinones as Selective Inhibitors of the X‑Linked Inhibitor of Apoptosis Protein (XIAP) Second Baculovirus IAP Repeat (BIR2) Domain

Journal of medicinal chemistry, 2013-10, Vol.56 (20), p.7788-7803

2013

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Methylene amine substituted arylindenopyrimidines as potent adenosine A(2A)/A(1) antagonists

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (9), p.2864-2867

2010

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Methylene amine substituted arylindenopyrimidines as potent adenosine A2A/A1 antagonists

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (9), p.2864-2867

2010

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Optimization of arylindenopyrimidines as potent adenosine A2A/A1 antagonists

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (9), p.2868-2871

2010

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Optimization of arylindenopyrimidines as potent adenosine A(2A)/A(1) antagonists

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (9), p.2868-2871

2010

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6-Amino-2-(4-fluorophenyl)-4-methoxy-3- (4-pyridyl)-1H-pyrrolo[2,3-b]pyridine (RWJ 68354): A Potent and Selective p38 Kinase Inhibitor

Journal of medicinal chemistry, 1998-10, Vol.41 (22), p.4196-4198

1998

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Synthesis of Verbenindenes: A New Class of Chiral Indenyl Ligands Derived from Verbenone

Organometallics, 2002-01, Vol.21 (1), p.144-149

2002

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In Vivo Characterization of a Dual Adenosine A 2A /A 1 Receptor Antagonist in Animal Models of Parkinson’s Disease

Journal of medicinal chemistry, 2010-11, Vol.53 (22), p.8104-8115

2010

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Suzuki Couplings with Phthalimidines - An Efficient Route to Staurosporinone Analogs

Heterocycles, 1997, Vol.45 (11), p.2217

1997

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Optimization of arylindenopyrimidines as potent adenosine A sub(2A)/A sub(1) antagonists

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (9), p.2868-2871

2010

Volltextzugriff (PDF)

Methylene amine substituted arylindenopyrimidines as potent adenosine A sub(2A)/A sub(1) antagonists

Bioorganic & medicinal chemistry letters, 2010-05, Vol.20 (9), p.2864-2867

2010

Volltextzugriff (PDF)

Methylene amine substituted arylindenopyrimidines as potent adenosine A 2A/A 1 antagonists

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (9), p.2864-2867

2010

Volltextzugriff (PDF)

Optimization of arylindenopyrimidines as potent adenosine A 2A/A 1 antagonists

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (9), p.2868-2871

2010

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Potent inhibitors of the MAP kinase p38

Bioorganic & medicinal chemistry letters, 1998-12, Vol.8 (23), p.3335-3340

1998

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The development of novel and selective p56lck tyrosine kinase inhibitors

Bioorganic & medicinal chemistry letters, 1998-09, Vol.8 (18), p.2489-2494

1998

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6-Amino-2-(4-fluorophenyl)-4-methoxy-3- (4-pyridyl)-1 H -pyrrolo[2,3- b ]pyridine (RWJ 68354): A Potent and Selective p38 Kinase Inhibitor

Journal of medicinal chemistry, 1998-10, Vol.41 (22), p.4196-4198

1998

Volltextzugriff (PDF)

The development of novel and selective p56 lck tyrosine kinase inhibitors

Bioorganic & medicinal chemistry letters, 1998, Vol.8 (18), p.2489-2494

1998

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Imidazopyrimidines, Potent Inhibitors of p38 MAP Kinase

ChemInform, 2003-06, Vol.34 (23), p.no-no

2003

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ChemInform Abstract: Potent Inhibitors of the MAP Kinase p38

ChemInform, 1999-03, Vol.30 (11), p.no-no

1999

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Colorectal cancer: texture analysis of portal phase hepatic CT images as a potential marker of survival

Radiology, 2009-02, Vol.250 (2), p.444

2009

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Texture analysis in non-contrast enhanced CT: Impact of malignancy on texture in apparently disease-free areas of the liver

European journal of radiology, 2009-04, Vol.70 (1), p.101-110

2009

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Spatial variability in tree regeneration after wildfire delays and dampens future bark beetle outbreaks

Proceedings of the National Academy of Sciences - PNAS, 2016-11, Vol.113 (46), p.13075-13080

2016

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Imidazopyrimidines, potent inhibitors of p38 MAP kinase

Benzazepinones and Benzoxazepinones as Antagonists of Inhibitor of Apoptosis Proteins (IAPs) Selective for the Second Baculovirus IAP Repeat (BIR2) Domain

In Vivo Characterization of a Dual Adenosine A2A/A1 Receptor Antagonist in Animal Models of Parkinson’s Disease

Optimization of Benzodiazepinones as Selective Inhibitors of the X‑Linked Inhibitor of Apoptosis Protein (XIAP) Second Baculovirus IAP Repeat (BIR2) Domain

Methylene amine substituted arylindenopyrimidines as potent adenosine A(2A)/A(1) antagonists

Methylene amine substituted arylindenopyrimidines as potent adenosine A2A/A1 antagonists

Optimization of arylindenopyrimidines as potent adenosine A2A/A1 antagonists

Optimization of arylindenopyrimidines as potent adenosine A(2A)/A(1) antagonists

6-Amino-2-(4-fluorophenyl)-4-methoxy-3- (4-pyridyl)-1H-pyrrolo[2,3-b]pyridine (RWJ 68354): A Potent and Selective p38 Kinase Inhibitor

Synthesis of Verbenindenes: A New Class of Chiral Indenyl Ligands Derived from Verbenone

In Vivo Characterization of a Dual Adenosine A 2A /A 1 Receptor Antagonist in Animal Models of Parkinson’s Disease

Suzuki Couplings with Phthalimidines - An Efficient Route to Staurosporinone Analogs

Optimization of arylindenopyrimidines as potent adenosine A sub(2A)/A sub(1) antagonists

Methylene amine substituted arylindenopyrimidines as potent adenosine A sub(2A)/A sub(1) antagonists

Methylene amine substituted arylindenopyrimidines as potent adenosine A 2A/A 1 antagonists

Optimization of arylindenopyrimidines as potent adenosine A 2A/A 1 antagonists

Potent inhibitors of the MAP kinase p38

The development of novel and selective p56lck tyrosine kinase inhibitors

6-Amino-2-(4-fluorophenyl)-4-methoxy-3- (4-pyridyl)-1 H -pyrrolo[2,3- b ]pyridine (RWJ 68354): A Potent and Selective p38 Kinase Inhibitor

The development of novel and selective p56 lck tyrosine kinase inhibitors

Imidazopyrimidines, Potent Inhibitors of p38 MAP Kinase

ChemInform Abstract: Potent Inhibitors of the MAP Kinase p38

Colorectal cancer: texture analysis of portal phase hepatic CT images as a potential marker of survival

Texture analysis in non-contrast enhanced CT: Impact of malignancy on texture in apparently disease-free areas of the liver

Spatial variability in tree regeneration after wildfire delays and dampens future bark beetle outbreaks

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