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...

Novel Small Molecule Inhibitors of 3-Phosphoinositide-dependent Kinase-1

The Journal of biological chemistry, 2005-05, Vol.280 (20), p.19867-19874

2005

Volltextzugriff (PDF)

Crystal Structures of Two Potent Nonamidine Inhibitors Bound to Factor Xa

Biochemistry (Easton), 2002-12, Vol.41 (52), p.15514-15523

2002

Volltextzugriff (PDF)

Thiophene-Anthranilamides as Highly Potent and Orally Available Factor Xa Inhibitors

Journal of medicinal chemistry, 2007-06, Vol.50 (13), p.2967-2980

2007

Volltextzugriff (PDF)

Indolinone based phosphoinositide-dependent kinase-1 (PDK1) inhibitors. Part 2: Optimization of BX- 517

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (14), p.3819-3825

2007

Volltextzugriff (PDF)

Indolinone based phosphoinositide-dependent kinase-1 (PDK1) inhibitors. Part 1: Design, synthesis and biological activity

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (14), p.3814-3818

2007

Volltextzugriff (PDF)

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase

Bioorganic & medicinal chemistry, 2008-05, Vol.16 (9), p.4963-4983

2008

Volltextzugriff (PDF)

Substituted thiophene-anthranilamides as potent inhibitors of human factor Xa

Bioorganic & medicinal chemistry, 2007-03, Vol.15 (5), p.2127-2146

2007

Volltextzugriff (PDF)

Structure–Activity relationships of substituted benzothiophene-anthranilamide factor Xa inhibitors

Bioorganic & medicinal chemistry letters, 2003-02, Vol.13 (3), p.507-511

2003

Volltextzugriff (PDF)

Inverse Electron Demand Diels-Alder Reactions of Heterocyclic Azadienes: [4 + 2] Cycloaddition Reaction of Amidines with 1,3,5-Triazines

Journal of organic chemistry, 1994-08, Vol.59 (17), p.4950-4955

1994

Volltextzugriff (PDF)

Design, Synthesis, and Biological Activity of Novel Factor Xa Inhibitors: 4-Aryloxy Substituents of 2,6-Diphenoxypyridines

Bioorganic & medicinal chemistry, 2002-03, Vol.10 (3), p.657-666

2002

Volltextzugriff (PDF)

Design, synthesis, and evaluation of potential GAR and AICAR transformylase inhibitors

Bioorganic & medicinal chemistry, 1998-06, Vol.6 (6), p.643-659

1998

Volltextzugriff (PDF)

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A(4) hydrolase

Bioorganic & medicinal chemistry, 2008-05, Vol.16 (9), p.4963

2008

Volltextzugriff (PDF)

Fluorine-18 labeled progestin ketals: synthesis and target tissue uptake selectivity of potential imaging agents for receptor-positive breast tumors

Journal of medicinal chemistry, 1993-04, Vol.36 (9), p.1120-1127

1993

Volltextzugriff (PDF)

Fluorine-substituted corticosteroids: Synthesis and evaluation as potential receptor-based imaging agents for positron emission tomography of the brain

International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology, 1992-05, Vol.19 (4), p.461-480

1992

Volltextzugriff (PDF)

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A sub(4) hydrolase

Bioorganic & medicinal chemistry, 2008-05, Vol.16 (9), p.4954-4962

2008

Volltextzugriff (PDF)

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A 4 hydrolase

Bioorganic & medicinal chemistry, 2008, Vol.16 (9), p.4963-4983

2008

Volltextzugriff (PDF)

Design, Synthesis, and Biological Activity of Novel Factor Xa Inhibitors: 4-Aryloxy Substituents of 2,6-Diphenoxypyridines††See ref. 1

Bioorganic & medicinal chemistry, 2002-03, Vol.10 (3), p.657-666

2002

Volltextzugriff (PDF)

Synthesis and NMR spectrum of [13C18]-meso-hexestrol, a fully carbon-13 substituted ligand for NMR studies of the estrogen receptor

Magnetic resonance in chemistry, 1993-11, Vol.31 (11), p.977-986

1993

Volltextzugriff (PDF)

Structure-Activity Relationships of Substituted Benzothiopheneanthranilamide Factor Xa Inhibitors

ChemInform, 2003-05, Vol.34 (21), p.no-no

2003

Volltextzugriff (PDF)

Predictions of CCR1 Chemokine Receptor Structure and BX 471 Antagonist Binding Followed by Experimental Validation

The Journal of biological chemistry, 2006-09, Vol.281 (37), p.27613-27620

2006

Volltextzugriff (PDF)

Regiospecific aryl nitration of meso-substituted tetraarylporphyrins: a simple route to bifunctional porphyrins

Journal of organic chemistry, 1989-05, Vol.54 (11), p.2753-2756

1989

Volltextzugriff (PDF)

Synthesis of N-alkyl glycine amides as potent inhibitors of leukotriene A4 hydrolase

Bioorganic & medicinal chemistry letters, 2008-07, Vol.18 (14), p.3891-3894

2008

Volltextzugriff (PDF)

Discovery of novel and potent aryl diamines as leukotriene A4 hydrolase inhibitors

Bioorganic & medicinal chemistry letters, 2008-07, Vol.18 (14), p.3895-3898

2008

Volltextzugriff (PDF)

Discovery of novel and potent aryl diamines as leukotriene A sub(4) hydrolase inhibitors

Bioorganic & medicinal chemistry, 2008-07, Vol.18 (14), p.3895-3898

2008

Volltextzugriff (PDF)

Discovery and characterization of a potent and selective non-amidine inhibitor of human factor Xa

Biochemical pharmacology, 2003-05, Vol.65 (9), p.1407-1418

2003

Volltextzugriff (PDF)

1 – 25 von 28

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(27)
Mit Volltextzugriff
(28)

Publikationsform

Artikel
(28)

Sprache

Englisch
(28)

Erscheinungsjahr

n.n

Thema

Science & Technology
(16)
Life Sciences & Biomedicine
(14)
Biological And Medical Sciences
(11)
Animals
(10)
Chemistry
(10)
Humans
(10)
Medical Sciences
(10)
Pharmacology & Pharmacy
(10)
Chemistry, Medicinal
(9)
Chemistry, Organic
(9)
Pharmacology. Drug Treatments
(9)
Physical Sciences
(9)
Structure-Activity Relationship
(8)
Biochemistry & Molecular Biology
(7)
Factor Xa Inhibitors
(6)
Models, Molecular
(6)
Drug Design
(5)
Rats
(5)
Blood. Blood Coagulation. Reticuloendothelial System
(4)
Crystal Structure
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Novel Small Molecule Inhibitors of 3-Phosphoinositide-dependent Kinase-1

Crystal Structures of Two Potent Nonamidine Inhibitors Bound to Factor Xa

Thiophene-Anthranilamides as Highly Potent and Orally Available Factor Xa Inhibitors

Indolinone based phosphoinositide-dependent kinase-1 (PDK1) inhibitors. Part 2: Optimization of BX- 517

Indolinone based phosphoinositide-dependent kinase-1 (PDK1) inhibitors. Part 1: Design, synthesis and biological activity

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase

Substituted thiophene-anthranilamides as potent inhibitors of human factor Xa

Structure–Activity relationships of substituted benzothiophene-anthranilamide factor Xa inhibitors

Inverse Electron Demand Diels-Alder Reactions of Heterocyclic Azadienes: [4 + 2] Cycloaddition Reaction of Amidines with 1,3,5-Triazines

Design, Synthesis, and Biological Activity of Novel Factor Xa Inhibitors: 4-Aryloxy Substituents of 2,6-Diphenoxypyridines

Design, synthesis, and evaluation of potential GAR and AICAR transformylase inhibitors

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A(4) hydrolase

Fluorine-18 labeled progestin ketals: synthesis and target tissue uptake selectivity of potential imaging agents for receptor-positive breast tumors

Fluorine-substituted corticosteroids: Synthesis and evaluation as potential receptor-based imaging agents for positron emission tomography of the brain

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A sub(4) hydrolase

Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A 4 hydrolase

Design, Synthesis, and Biological Activity of Novel Factor Xa Inhibitors: 4-Aryloxy Substituents of 2,6-Diphenoxypyridines††See ref. 1

Synthesis and NMR spectrum of [13C18]-meso-hexestrol, a fully carbon-13 substituted ligand for NMR studies of the estrogen receptor

Structure-Activity Relationships of Substituted Benzothiopheneanthranilamide Factor Xa Inhibitors

Predictions of CCR1 Chemokine Receptor Structure and BX 471 Antagonist Binding Followed by Experimental Validation

Regiospecific aryl nitration of meso-substituted tetraarylporphyrins: a simple route to bifunctional porphyrins

Synthesis of N-alkyl glycine amides as potent inhibitors of leukotriene A4 hydrolase

Discovery of novel and potent aryl diamines as leukotriene A4 hydrolase inhibitors

Discovery of novel and potent aryl diamines as leukotriene A sub(4) hydrolase inhibitors

Discovery and characterization of a potent and selective non-amidine inhibitor of human factor Xa

Suchergebnisse filtern