UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Perspectives and Opportunities in Medicinal Chemistry: A View from the Novartis Institute for BioMedical Research Institute in Basel, Switzerland: A Perspective on Chemistry and Society : A Column on the Occasion of the 75th Anniversary of CHIMIA

Chimia, 2021-12, Vol.75 (12), p.1091

2021

Volltextzugriff (PDF)

Perspectives and Opportunities in Medicinal Chemistry: A View from the Novartis Institute for BioMedical Research in Basel, Switzerland

Chimia, 2021-12, Vol.75 (12), p.1091

2021

Volltextzugriff (PDF)

European Medicinal Chemistry Leaders in Industry (EMCL) – On the Status and Future of Medicinal Chemistry Research in Europe

ChemMedChem, 2023-07, Vol.18 (13), p.e202300127-n/a

2023

Volltextzugriff (PDF)

N7-Substituted-5-aryl-pyrrolo[2,3-d]pyrimidines Represent a Versatile Class of Potent Inhibitors of the Tyrosine Kinase c-Src

Mini reviews in medicinal chemistry, 2002-06, Vol.2 (3), p.201-208

2002

Volltextzugriff (PDF)

Novel Purine Nitrile Derived Inhibitors of the Cysteine Protease Cathepsin K

Journal of medicinal chemistry, 2004-11, Vol.47 (24), p.5833-5836

2004

Volltextzugriff (PDF)

A Solid-Phase Assay for the Determination of Protein Tyrosine Kinase Activity of c-src Using Scintillating Microtitration Plates

Analytical biochemistry, 1996-02, Vol.234 (1), p.23-26

1996

Volltextzugriff (PDF)

1-Alkyl-4-phenyl-6-alkoxy-1H-quinazolin-2-ones: A Novel Series of Potent Calcium-Sensing Receptor Antagonists

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.2250-2263

2010

Volltextzugriff (PDF)

2-Cyano-pyrimidines: A New Chemotype for Inhibitors of the Cysteine Protease Cathepsin K

Journal of medicinal chemistry, 2007-02, Vol.50 (4), p.591-594

2007

Volltextzugriff (PDF)

Pineal gland hormone melatonin binds and activates an orphan of the nuclear receptor superfamily

The Journal of biological chemistry, 1994-11, Vol.269 (46), p.28531-28534

1994

Volltextzugriff (PDF)

Novel scaffold for cathepsin K inhibitors

Bioorganic & medicinal chemistry, 2007-11, Vol.17 (22), p.6096-6100

2007

Volltextzugriff (PDF)

Transcriptional activation of the nuclear receptor RZRα by the pineal gland hormone melatonin and identification of CGP 52608 as a synthetic ligand

Nucleic acids research, 1995-02, Vol.23 (3), p.327-333

1995

Volltextzugriff (PDF)

Penta-substituted benzimidazoles as potent antagonists of the calcium-sensing receptor (CaSR-antagonists)

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (17), p.5161-5164

2010

Volltextzugriff (PDF)

Preface

Current pharmaceutical design, 2002-10, Vol.8 (23), p.i-i

2002

Volltextzugriff (PDF)

Dipeptide nitrile inhibitors of cathepsin K

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (9), p.2549-2554

2006

Volltextzugriff (PDF)

N(7)-substituted-5-aryl-pyrrolo[2,3-d]pyrimidines represent a versatile class of potent inhibitors of the tyrosine kinase c-Src

Mini reviews in medicinal chemistry, 2002-06, Vol.2 (3), p.201

2002

Volltextzugriff (PDF)

7-Alkyl- and 7-Cycloalkyl-5-aryl-pyrrolo[2,3- d]pyrimidines—potent inhibitors of the tyrosine kinase c-Src

Bioorganic & medicinal chemistry letters, 2001-03, Vol.11 (6), p.849-852

2001

Volltextzugriff (PDF)

Thiazolidine Diones, Specific Ligands of the Nuclear Receptor Retinoid Z Receptor/Retinoid Acid Receptor-related Orphan Receptor α with Potent Antiarthritic Activity

The Journal of biological chemistry, 1996-06, Vol.271 (23), p.13515-13522

1996

Volltextzugriff (PDF)

1-Alkyl-4-phenyl-6-alkoxy-1 H -quinazolin-2-ones: A Novel Series of Potent Calcium-Sensing Receptor Antagonists

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.2250-2263

2010

Volltextzugriff (PDF)

7-Pyrrolidinyl- and 7-piperidinyl-5-aryl-pyrrolo[2,3- d]pyrimidines—potent inhibitors of the tyrosine kinase c-Src

Bioorganic & medicinal chemistry letters, 2001-03, Vol.11 (6), p.853-856

2001

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

Volltextzugriff (PDF)

[3 + 3]-Carbocyclizations of nitroallylic esters and enamines with stereoselective formation of up to six new stereogenic centers

Journal of the American Chemical Society, 1990-10, Vol.112 (21), p.7625-7638

1990

Volltextzugriff (PDF)

Pineal gland hormone melatonin binds and activates an orphan of the nuclear receptor superfamily

The Journal of biological chemistry, 1997-06, Vol.272 (26), p.16707-16707

1997

Volltextzugriff (PDF)

Active Recombinant Human Tyrosine Kinase c-Yes: Expression in Baculovirus System, Purification, Comparison to c-Src, and Inhibition by a c-Src Inhibitor

Protein expression and purification, 2000-06, Vol.19 (1), p.99-106

2000

Volltextzugriff (PDF)

Specific Activation of the Nuclear Receptors PPARÎ³ and RORA by the Antidiabetic Thiazolidinedione BRL 49653 and the Antiarthritic Thiazolidinedione Derivative CGP 52608

Molecular pharmacology, 1998-06, Vol.53 (6), p.1131

1998

Volltextzugriff (PDF)

Thiazolidine Diones, Specific Ligands of the Nuclear Receptor Retinoid Z Receptor/Retinoid Acid Receptor-related Orphan Receptor Î± with Potent Antiarthritic Activity

The Journal of biological chemistry, 1996-06, Vol.271 (23), p.13515

1996

Volltextzugriff (PDF)

1 – 25 von 38

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(34)
Mit Volltextzugriff
(32)

Publikationsform

Artikel
(38)

Sprache

Englisch
(38)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Perspectives and Opportunities in Medicinal Chemistry: A View from the Novartis Institute for BioMedical Research Institute in Basel, Switzerland: A Perspective on Chemistry and Society : A Column on the Occasion of the 75th Anniversary of CHIMIA

Perspectives and Opportunities in Medicinal Chemistry: A View from the Novartis Institute for BioMedical Research in Basel, Switzerland

European Medicinal Chemistry Leaders in Industry (EMCL) – On the Status and Future of Medicinal Chemistry Research in Europe

N7-Substituted-5-aryl-pyrrolo[2,3-d]pyrimidines Represent a Versatile Class of Potent Inhibitors of the Tyrosine Kinase c-Src

Novel Purine Nitrile Derived Inhibitors of the Cysteine Protease Cathepsin K

A Solid-Phase Assay for the Determination of Protein Tyrosine Kinase Activity of c-src Using Scintillating Microtitration Plates

1-Alkyl-4-phenyl-6-alkoxy-1H-quinazolin-2-ones: A Novel Series of Potent Calcium-Sensing Receptor Antagonists

2-Cyano-pyrimidines: A New Chemotype for Inhibitors of the Cysteine Protease Cathepsin K

Pineal gland hormone melatonin binds and activates an orphan of the nuclear receptor superfamily

Novel scaffold for cathepsin K inhibitors

Transcriptional activation of the nuclear receptor RZRα by the pineal gland hormone melatonin and identification of CGP 52608 as a synthetic ligand

Penta-substituted benzimidazoles as potent antagonists of the calcium-sensing receptor (CaSR-antagonists)

Preface

Dipeptide nitrile inhibitors of cathepsin K

N(7)-substituted-5-aryl-pyrrolo[2,3-d]pyrimidines represent a versatile class of potent inhibitors of the tyrosine kinase c-Src

7-Alkyl- and 7-Cycloalkyl-5-aryl-pyrrolo[2,3- d]pyrimidines—potent inhibitors of the tyrosine kinase c-Src

Thiazolidine Diones, Specific Ligands of the Nuclear Receptor Retinoid Z Receptor/Retinoid Acid Receptor-related Orphan Receptor α with Potent Antiarthritic Activity

1-Alkyl-4-phenyl-6-alkoxy-1 H -quinazolin-2-ones: A Novel Series of Potent Calcium-Sensing Receptor Antagonists

7-Pyrrolidinyl- and 7-piperidinyl-5-aryl-pyrrolo[2,3- d]pyrimidines—potent inhibitors of the tyrosine kinase c-Src

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

[3 + 3]-Carbocyclizations of nitroallylic esters and enamines with stereoselective formation of up to six new stereogenic centers

Pineal gland hormone melatonin binds and activates an orphan of the nuclear receptor superfamily

Active Recombinant Human Tyrosine Kinase c-Yes: Expression in Baculovirus System, Purification, Comparison to c-Src, and Inhibition by a c-Src Inhibitor

Specific Activation of the Nuclear Receptors PPARÎ³ and RORA by the Antidiabetic Thiazolidinedione BRL 49653 and the Antiarthritic Thiazolidinedione Derivative CGP 52608

Thiazolidine Diones, Specific Ligands of the Nuclear Receptor Retinoid Z Receptor/Retinoid Acid Receptor-related Orphan Receptor Î± with Potent Antiarthritic Activity

Suchergebnisse filtern