UB Paderborn / Katalog / Suche / in CDI

Discovery of a Novel 2,6-Disubstituted Glucosamine Series of Potent and Selective Hexokinase 2 Inhibitors

ACS medicinal chemistry letters, 2016-03, Vol.7 (3), p.217-222

2016

Link zum Volltext

Verfügbarkeit prüfen

Structural Basis for Chk1 Inhibition by UCN-01

The Journal of biological chemistry, 2002-11, Vol.277 (48), p.46609-46615

2002

Link zum Volltext

Verfügbarkeit prüfen

Measuring the performance of green investment portfolios for zero-carbon environment: a comparative analysis of digital finance and asset-backed securities

Environmental science and pollution research international, 2024-01, Vol.31 (1), p.357-370

2024

Link zum Volltext

Verfügbarkeit prüfen

Design and synthesis of orally bioavailable serum and glucocorticoid-regulated kinase 1 (SGK1) inhibitors

Bioorganic & medicinal chemistry letters, 2009-08, Vol.19 (15), p.4441-4445

2009

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of Chk1 by the G2 DNA damage checkpoint inhibitor isogranulatimide

Molecular cancer therapeutics, 2004-10, Vol.3 (10), p.1221-1227

2004

Link zum Volltext

Verfügbarkeit prüfen

Nurturing knowledge absorption in the organizations: examining the role of transformational leadership, learning climate, and proactive personality

Current psychology (New Brunswick, N.J.), 2024-05, Vol.43 (17), p.15959-15970

2024

Link zum Volltext

Verfügbarkeit prüfen

N-Phenyl- N-purin-6-yl ureas: The design and synthesis of p38α MAP kinase inhibitors

Bioorganic & medicinal chemistry letters, 2003-03, Vol.13 (6), p.1191-1194

2003

Link zum Volltext

Verfügbarkeit prüfen

Design, synthesis and selection of DNA-encoded small-molecule libraries

Nature Chemical Biology, 2009-09, Vol.5 (9), p.647-654

2009

Link zum Volltext

Verfügbarkeit prüfen

Cyclic Ketone Inhibitors of the Cysteine Protease Cathepsin K

Journal of medicinal chemistry, 2001-03, Vol.44 (5), p.725-736

2001

Link zum Volltext

Verfügbarkeit prüfen

Modulation of kinase‐inhibitor interactions by auxiliary protein binding: Crystallography studies on Aurora A interactions with VX‐680 and with TPX2

Protein science, 2008-10, Vol.17 (10), p.1791-1797

2008

Link zum Volltext

Verfügbarkeit prüfen

Use of Papain as a Model for the Structure-Based Design of Cathepsin K Inhibitors: Crystal Structures of Two Papain−Inhibitor Complexes Demonstrate Binding to S‘-Subsites

Journal of medicinal chemistry, 1998-11, Vol.41 (23), p.4567-4576

1998

Link zum Volltext

Verfügbarkeit prüfen

Conformationally Constrained 1,3-Diamino Ketones: A Series of Potent Inhibitors of the Cysteine Protease Cathepsin K

Journal of medicinal chemistry, 1998-09, Vol.41 (19), p.3563-3567

1998

Link zum Volltext

Verfügbarkeit prüfen

The Amino-Acid Substituents of Dipeptide Substrates of Cathepsin C Can Determine the Rate-Limiting Steps of Catalysis

Biochemistry (Easton), 2012-09, Vol.51 (38), p.7551-7568

2012

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of human immunodeficiency virus-1 protease by a C2-symmetric phosphinate. Synthesis and crystallographic analysis

Biochemistry (Easton), 1993-08, Vol.32 (31), p.7972-7980

1993

Link zum Volltext

Verfügbarkeit prüfen

Human Immunodeficiency Virus Protease Ligand Specificity Conferred by Residues Outside of the Active Site Cavity

Biochemistry (Easton), 1996-08, Vol.35 (32), p.10279-10286

1996

Link zum Volltext

Verfügbarkeit prüfen

Crystal structure of the kinase domain of serum and glucocorticoid‐regulated kinase 1 in complex with AMP–PNP

Protein science, 2007-12, Vol.16 (12), p.2761-2769

2007

Link zum Volltext

Verfügbarkeit prüfen

Rational Design, Synthesis, and Crystallographic Analysis of a Hydroxyethylene-Based HIV-1 Protease Inhibitor Containing a Heterocyclic P1'-P2' Amide Bond Isostere

Journal of medicinal chemistry, 1994-09, Vol.37 (19), p.3100-3107

1994

Link zum Volltext

Verfügbarkeit prüfen

Structure-Based Design of Cathepsin K Inhibitors Containing a Benzyloxy-Substituted Benzoyl Peptidomimetic

Journal of medicinal chemistry, 1998-10, Vol.41 (21), p.3923-3927

1998

Link zum Volltext

Verfügbarkeit prüfen

Discovery of Novel Cyanamide-Based Inhibitors of Cathepsin C

ACS medicinal chemistry letters, 2011-02, Vol.2 (2), p.142-147

2011

Link zum Volltext

Verfügbarkeit prüfen

A Check on Rational Drug Design: Crystal Structure of a Complex of Human Immunodeficiency Virus Type 1 Protease with a Novel .gamma.-Turn Mimetic Inhibitor

Journal of medicinal chemistry, 1995-08, Vol.38 (17), p.3246-3252

1995

Link zum Volltext

Verfügbarkeit prüfen

Directional pilot protection method for distribution grid with DG

12th IET International Conference on Developments in Power System Protection (DPSP 2014), 2014, p.12.07

2014

Link zum Volltext

Verfügbarkeit prüfen

Kinetic Mechanism and Rate-Limiting Steps of Focal Adhesion Kinase-1

Biochemistry (Easton), 2010-08, Vol.49 (33), p.7151-7163

2010

Link zum Volltext

Verfügbarkeit prüfen

Analysis on transfer characteristics of Rogowski coil transducer to travelling wave

2011 International Conference on Advanced Power System Automation and Protection, 2011, Vol.2, p.1056-1059

2011

Link zum Volltext
IEEE_Xplore

A New Approach of Determination of Comprehensive Weight in Condition Assessment of Power Transformer

Applied Mechanics and Materials, 2013, Vol.273, p.365-370

2013

Link zum Volltext

Verfügbarkeit prüfen

Structure Activity Relationships of 5-, 6-, and 7-Methyl-Substituted Azepan-3-one Cathepsin K Inhibitors

Journal of medicinal chemistry, 2006-03, Vol.49 (5), p.1597-1612

2006

Link zum Volltext

Verfügbarkeit prüfen

Menü

Weitere Dienste

Einstellungen

Discovery of a Novel 2,6-Disubstituted Glucosamine Series of Potent and Selective Hexokinase 2 Inhibitors

Structural Basis for Chk1 Inhibition by UCN-01

Measuring the performance of green investment portfolios for zero-carbon environment: a comparative analysis of digital finance and asset-backed securities

Design and synthesis of orally bioavailable serum and glucocorticoid-regulated kinase 1 (SGK1) inhibitors

Inhibition of Chk1 by the G2 DNA damage checkpoint inhibitor isogranulatimide

Nurturing knowledge absorption in the organizations: examining the role of transformational leadership, learning climate, and proactive personality

N-Phenyl- N-purin-6-yl ureas: The design and synthesis of p38α MAP kinase inhibitors

Design, synthesis and selection of DNA-encoded small-molecule libraries

Cyclic Ketone Inhibitors of the Cysteine Protease Cathepsin K

Modulation of kinase‐inhibitor interactions by auxiliary protein binding: Crystallography studies on Aurora A interactions with VX‐680 and with TPX2

Use of Papain as a Model for the Structure-Based Design of Cathepsin K Inhibitors: Crystal Structures of Two Papain−Inhibitor Complexes Demonstrate Binding to S‘-Subsites

Conformationally Constrained 1,3-Diamino Ketones: A Series of Potent Inhibitors of the Cysteine Protease Cathepsin K

The Amino-Acid Substituents of Dipeptide Substrates of Cathepsin C Can Determine the Rate-Limiting Steps of Catalysis

Inhibition of human immunodeficiency virus-1 protease by a C2-symmetric phosphinate. Synthesis and crystallographic analysis

Human Immunodeficiency Virus Protease Ligand Specificity Conferred by Residues Outside of the Active Site Cavity

Crystal structure of the kinase domain of serum and glucocorticoid‐regulated kinase 1 in complex with AMP–PNP

Rational Design, Synthesis, and Crystallographic Analysis of a Hydroxyethylene-Based HIV-1 Protease Inhibitor Containing a Heterocyclic P1'-P2' Amide Bond Isostere

Structure-Based Design of Cathepsin K Inhibitors Containing a Benzyloxy-Substituted Benzoyl Peptidomimetic

Discovery of Novel Cyanamide-Based Inhibitors of Cathepsin C

A Check on Rational Drug Design: Crystal Structure of a Complex of Human Immunodeficiency Virus Type 1 Protease with a Novel .gamma.-Turn Mimetic Inhibitor

Directional pilot protection method for distribution grid with DG

Kinetic Mechanism and Rate-Limiting Steps of Focal Adhesion Kinase-1

Analysis on transfer characteristics of Rogowski coil transducer to travelling wave

A New Approach of Determination of Comprehensive Weight in Condition Assessment of Power Transformer

Structure Activity Relationships of 5-, 6-, and 7-Methyl-Substituted Azepan-3-one Cathepsin K Inhibitors

Suchergebnisse filtern