UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 157

Sortiert nach

Discovery of ABT-957: 1-Benzyl-5-oxopyrrolidine-2-carboxamides as selective calpain inhibitors with enhanced metabolic stability

Bioorganic & medicinal chemistry letters, 2019-08, Vol.29 (15), p.1968-1973

2019

Link zum Volltext

Verfügbarkeit prüfen

Rho kinase, a promising drug target for neurological disorders

Nature reviews. Drug discovery, 2005-05, Vol.4 (5), p.387-398

2005

Link zum Volltext

Verfügbarkeit prüfen

Discovery of Novel and Highly Selective Inhibitors of Calpain for the Treatment of Alzheimer’s Disease: 2‑(3-Phenyl‑1H‑pyrazol-1-yl)-nicotinamides

Journal of medicinal chemistry, 2017-08, Vol.60 (16), p.7123-7138

2017

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of Rho kinase (ROCK) increases neurite outgrowth on chondroitin sulphate proteoglycan in vitro and axonal regeneration in the adult optic nerve in vivo

Journal of neurochemistry, 2007-10, Vol.103 (1), p.181-189

2007

Link zum Volltext

Verfügbarkeit prüfen

A new mild method for the synthesis of amidines

Tetrahedron letters, 1999-09, Vol.40 (39), p.7067-7070

1999

Link zum Volltext

Verfügbarkeit prüfen

Mitigating the Metabolic Liability of Carbonyl Reduction: Novel Calpain Inhibitors with P1′ Extension

ACS medicinal chemistry letters, 2018-03, Vol.9 (3), p.221-226

2018

Link zum Volltext

Verfügbarkeit prüfen

A-1048400 is a novel, orally active, state-dependent neuronal calcium channel blocker that produces dose-dependent antinociception without altering hemodynamic function in rats

Biochemical pharmacology, 2012-02, Vol.83 (3), p.406-418

2012

Link zum Volltext

Verfügbarkeit prüfen

The Spinning Disk Reactor for Polymers and Nanoparticles

Macromolecular reaction engineering, 2013-02, Vol.7 (2), p.98-106

2013

Link zum Volltext

Verfügbarkeit prüfen

Discovery of diphenyl lactam derivatives as N-type calcium channel blockers

Bioorganic & medicinal chemistry letters, 2012-02, Vol.22 (4), p.1716-1718

2012

Link zum Volltext

Verfügbarkeit prüfen

Characterization of the Cardiovascular Profile of Two Novel Ca 2+ Channels Blockers

The FASEB journal, 2011-04, Vol.25 (S1)

2011

Link zum Volltext

Verfügbarkeit prüfen

Characterization of the Cardiovascular Profile of Two Novel Ca2+ Channels Blockers

The FASEB journal, 2011, Vol.25, p.1021.14-1021.14

2011

Link zum Volltext

Verfügbarkeit prüfen

Technical Scale Synthesis of a New and Highly Potent Thrombin Inhibitor

Synthesis (Stuttgart), 2004, Vol.2004 (14), p.2367-2375

2004

Link zum Volltext

Verfügbarkeit prüfen

Orally active thrombin inhibitors. Part 2: Optimization of the P2-moiety

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (10), p.2648-2653

2006

Link zum Volltext

Verfügbarkeit prüfen

Synthesis and SAR of highly potent dual 5-HT1A and 5-HT1B antagonists as potential antidepressant drugs

Bioorganic & medicinal chemistry letters, 2005-12, Vol.15 (24), p.5567-5573

2005

Link zum Volltext

Verfügbarkeit prüfen

Technical Scale Synthesis of a New and Highly Potent Thrombin Inhibitor

Synthesis (Stuttgart), 2004-10, Vol.2004 (14), p.2367-2375

2004

Link zum Volltext

Verfügbarkeit prüfen

Orally active thrombin inhibitors. Part 1: Optimization of the P1-moiety

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (10), p.2641-2647

2006

Link zum Volltext

Verfügbarkeit prüfen

Synthesis, characterization and reactivity of amido titanium and zirconium complexes

Journal of organometallic chemistry, 1996-11, Vol.525 (1), p.81-87

1996

Link zum Volltext

Verfügbarkeit prüfen

Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective alpha(V)beta(3) antagonists

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (3), p.441-446

2002

Link zum Volltext

Verfügbarkeit prüfen

Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective αVβ3 antagonists

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (3), p.441-446

2002

Link zum Volltext

Verfügbarkeit prüfen

d-Phe-Pro-Arg type thrombin inhibitors: unexpected selectivity by modification of the P1 moiety

Bioorganic & medicinal chemistry letters, 2003-06, Vol.13 (12), p.2029-2033

2003

Link zum Volltext

Verfügbarkeit prüfen

Thermal decomposition of [Me3SiNCH2CH2NSiMe3] · Li2(THF)2 to [LiN(SiMe3)2 · THF]2 via a 1,4-trimethylsilyl shift

Journal of organometallic chemistry, 1997-12, Vol.549 (1-2), p.39-43

1997

Link zum Volltext

Verfügbarkeit prüfen

Synthesis and SAR of highly potent dual 5-HT 1A and 5-HT 1B antagonists as potential antidepressant drugs

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (24), p.5567-5573

2005

Link zum Volltext

Verfügbarkeit prüfen

Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective α Vβ 3 antagonists

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (3), p.441-446

2002

Link zum Volltext

Verfügbarkeit prüfen

Thermal decomposition of [Me 3SiNCH 2CH 2NSiMe 3] · Li 2(THF) 2 to [LiN(SiMe3) 2 · THF] 2 via a 1,4-trimethylsilyl shift

Journal of organometallic chemistry, 1997, Vol.549 (1), p.39-43

1997

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 157

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(151)

Publikationsform

Sprache

Deutsch
(99)
Englisch
(56)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Discovery of ABT-957: 1-Benzyl-5-oxopyrrolidine-2-carboxamides as selective calpain inhibitors with enhanced metabolic stability

Rho kinase, a promising drug target for neurological disorders

Discovery of Novel and Highly Selective Inhibitors of Calpain for the Treatment of Alzheimer’s Disease: 2‑(3-Phenyl‑1H‑pyrazol-1-yl)-nicotinamides

Inhibition of Rho kinase (ROCK) increases neurite outgrowth on chondroitin sulphate proteoglycan in vitro and axonal regeneration in the adult optic nerve in vivo

A new mild method for the synthesis of amidines

Identification of Selective Dual ROCK1 and ROCK2 Inhibitors Using Structure-Based Drug Design

Mitigating the Metabolic Liability of Carbonyl Reduction: Novel Calpain Inhibitors with P1′ Extension

A-1048400 is a novel, orally active, state-dependent neuronal calcium channel blocker that produces dose-dependent antinociception without altering hemodynamic function in rats

The Spinning Disk Reactor for Polymers and Nanoparticles

Discovery of diphenyl lactam derivatives as N-type calcium channel blockers

Characterization of the Cardiovascular Profile of Two Novel Ca 2+ Channels Blockers

Characterization of the Cardiovascular Profile of Two Novel Ca2+ Channels Blockers

Technical Scale Synthesis of a New and Highly Potent Thrombin Inhibitor

Orally active thrombin inhibitors. Part 2: Optimization of the P2-moiety

Synthesis and SAR of highly potent dual 5-HT1A and 5-HT1B antagonists as potential antidepressant drugs

Technical Scale Synthesis of a New and Highly Potent Thrombin Inhibitor

Orally active thrombin inhibitors. Part 1: Optimization of the P1-moiety

Synthesis, characterization and reactivity of amido titanium and zirconium complexes

Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective alpha(V)beta(3) antagonists

Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective αVβ3 antagonists

d-Phe-Pro-Arg type thrombin inhibitors: unexpected selectivity by modification of the P1 moiety

Thermal decomposition of [Me3SiNCH2CH2NSiMe3] · Li2(THF)2 to [LiN(SiMe3)2 · THF]2 via a 1,4-trimethylsilyl shift

Synthesis and SAR of highly potent dual 5-HT 1A and 5-HT 1B antagonists as potential antidepressant drugs

Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective α Vβ 3 antagonists

Thermal decomposition of [Me 3SiNCH 2CH 2NSiMe 3] · Li 2(THF) 2 to [LiN(SiMe3) 2 · THF] 2 via a 1,4-trimethylsilyl shift

Suchergebnisse filtern