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...

Identification and biological activity of 6-alkyl-substituted 3-methyl-pyridine-2-carbonyl amino dimethyl-benzoic acid EP4 antagonists

Bioorganic & medicinal chemistry letters, 2016-05, Vol.26 (9), p.2303-2307

2016

Volltextzugriff (PDF)

Discovery and characterization of [(cyclopentyl)ethyl]benzoic acid inhibitors of microsomal prostaglandin E synthase-1

Bioorganic & medicinal chemistry letters, 2017-03, Vol.27 (6), p.1478-1483

2017

Volltextzugriff (PDF)

Characterization of 3,3-dimethyl substituted N-aryl piperidines as potent microsomal prostaglandin E synthase-1 inhibitors

Bioorganic & medicinal chemistry letters, 2016-10, Vol.26 (19), p.4824-4828

2016

Volltextzugriff (PDF)

Discovery of potent aryl-substituted 3-[(3-methylpyridine-2-carbonyl) amino]-2,4-dimethyl-benzoic acid EP4 antagonists with improved pharmacokinetic profile

Bioorganic & medicinal chemistry letters, 2016-02, Vol.26 (3), p.931-935

2016

Volltextzugriff (PDF)

Discovery of substituted-2,4-dimethyl-(naphthalene-4-carbonyl)amino-benzoic acid as potent and selective EP4 antagonists

Bioorganic & medicinal chemistry letters, 2016-01, Vol.26 (1), p.105-109

2016

Volltextzugriff (PDF)

Discovery and characterization of a potent and selective EP4 receptor antagonist

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (16), p.3176-3178

2015

Volltextzugriff (PDF)

Analgesic and anti‐inflammatory properties of novel, selective, and potent EP4 receptor antagonists

Pharmacology research & perspectives, 2017-06, Vol.5 (3), p.e00316-n/a

2017

Volltextzugriff (PDF)

Design and Synthesis of 2-Methyl-2-{4-[2-(5-methyl-2-aryloxazol- 4-yl)ethoxy]phenoxy}propionic Acids: A New Class of Dual PPARα/γ Agonists

Journal of medicinal chemistry, 2001-06, Vol.44 (13), p.2061-2064

2001

Volltextzugriff (PDF)

2-Alkoxydihydrocinnamates as PPAR agonists. Activity modulation by the incorporation of phenoxy substituents

Bioorganic & medicinal chemistry letters, 2005-01, Vol.15 (1), p.51-55

2005

Volltextzugriff (PDF)

Asymmetric total synthesis of dibenzocyclooctadiene lignans (-)-schizandrin and (-)-isoschizandrin. Structure revision of (+)-isoschizandrin

Journal of the American Chemical Society, 1990-10, Vol.112 (22), p.8090-8099

1990

Volltextzugriff (PDF)

Design and synthesis of novel and potent amide linked PPARγ/δ dual agonists

Bioorganic & medicinal chemistry letters, 2007-12, Vol.17 (24), p.6744-6749

2007

Volltextzugriff (PDF)

Tetrahydroisoquinoline PPARγ agonists: Design of novel, highly selective non-TZD antihyperglycemic agents

Bioorganic & medicinal chemistry letters, 2006-12, Vol.16 (24), p.6293-6297

2006

Volltextzugriff (PDF)

Synthesis and evaluation of aminomethyl dihydrocinnamates as a new class of PPAR ligands

Bioorganic & medicinal chemistry letters, 2006-12, Vol.16 (24), p.6328-6333

2006

Volltextzugriff (PDF)

Inhibition of thrombin activatable fibrinolysis inhibitor by cysteine derivatives

Thrombosis research, 2005, Vol.116 (3), p.265-271

2005

Volltextzugriff (PDF)

Discovery and characterization of [(cyclopentyl)ethyl]benzoic acid inhibitors of microsomal prostaglandin E synthase-1

Bioorganic & medicinal chemistry letters, 2017-03, Vol.27 (6)

2017

Volltextzugriff (PDF)

Characterization of 3,3-dimethyl substituted N-aryl piperidines as potent microsomal prostaglandin E synthase-1 inhibitors

Bioorganic & medicinal chemistry letters, 2016-10, Vol.26 (19)

2016

Volltextzugriff (PDF)

Synthesis of N,N‘-Orthogonally Protected (S)-Piperazine-2-carboxylic Acid

Journal of organic chemistry, 1997-09, Vol.62 (18), p.6439-6440

1997

Volltextzugriff (PDF)

A Peroxisome Proliferator-Activated Receptor α/γ Dual Agonist with a Unique in Vitro Profile and Potent Glucose and Lipid Effects in Rodent Models of Type 2 Diabetes and Dyslipidemia

Molecular endocrinology (Baltimore, Md.), 2005-06, Vol.19 (6), p.1593-1605

2005

Volltextzugriff (PDF)

An approach toward the ophiobolane sesterterpenes: synthesis of the ceroplastin nucleus

Journal of organic chemistry, 1990-05, Vol.55 (10), p.3075-3087

1990

Volltextzugriff (PDF)

Peroxisome Proliferator‐Activated Receptor γ Modulation for the Treatment of Type 2 Diabetes

Nuclear Receptors as Drug Targets, 2008, p.367-387

2008

Volltextzugriff (PDF)

Tetrahydroisoquinoline PPARgamma agonists: design of novel, highly selective non-TZD antihyperglycemic agents

Bioorganic & medicinal chemistry letters, 2006-12, Vol.16 (24), p.6293-6297

2006

Volltextzugriff (PDF)

Tetrahydroisoquinoline PPARrγ agonists : Design of novel, highly selective non-TZD antihyperglycemic agents

Bioorganic & medicinal chemistry letters, 2006, Vol.16 (24), p.6293-6297

2006

Volltextzugriff (PDF)

The synthesis of aminobenzazepinones as anti-phenylalanine dipeptide mimics and their use in nep inhibition

Bioorganic & medicinal chemistry letters, 1996-04, Vol.6 (8), p.957-962

1996

Volltextzugriff (PDF)

Design and synthesis of novel and potent amide linked PPARgamma/delta dual agonists

Bioorganic & medicinal chemistry letters, 2007-12, Vol.17 (24), p.6744-6749

2007

Volltextzugriff (PDF)

1 – 25 von 48

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(45)
Mit Volltextzugriff
(46)

Publikationsform

Sprache

Englisch
(48)

Erscheinungsjahr

n.n

Thema

Science & Technology
(31)
Life Sciences & Biomedicine
(26)
Animals
(20)
Humans
(18)
Rats
(16)
Chemistry
(15)
Physical Sciences
(15)
Chemistry, Organic
(14)
Pharmacology & Pharmacy
(14)
Chemistry, Medicinal
(13)
Biological And Medical Sciences
(10)
Low Density Lipoprotein Receptor-Related Protein-1
(10)
Receptors, Immunologic - Metabolism
(10)
Structure-Activity Relationship
(10)
Protein Binding
(8)
Tissue Plasminogen Activator - Metabolism
(8)
Kinetics
(7)
Binding Sites
(6)
Biochemistry & Molecular Biology
(6)
Medical Sciences
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Discovery of LY3104607: A Potent and Selective G Protein-Coupled Receptor 40 (GPR40) Agonist with Optimized Pharmacokinetic Properties to Support Once Daily Oral Treatment in Patients with Type 2 Diabetes Mellitus

Identification and biological activity of 6-alkyl-substituted 3-methyl-pyridine-2-carbonyl amino dimethyl-benzoic acid EP4 antagonists

Discovery and characterization of [(cyclopentyl)ethyl]benzoic acid inhibitors of microsomal prostaglandin E synthase-1

Characterization of 3,3-dimethyl substituted N-aryl piperidines as potent microsomal prostaglandin E synthase-1 inhibitors

Discovery of potent aryl-substituted 3-[(3-methylpyridine-2-carbonyl) amino]-2,4-dimethyl-benzoic acid EP4 antagonists with improved pharmacokinetic profile

Discovery of substituted-2,4-dimethyl-(naphthalene-4-carbonyl)amino-benzoic acid as potent and selective EP4 antagonists

Discovery and characterization of a potent and selective EP4 receptor antagonist

Analgesic and anti‐inflammatory properties of novel, selective, and potent EP4 receptor antagonists

Design and Synthesis of 2-Methyl-2-{4-[2-(5-methyl-2-aryloxazol- 4-yl)ethoxy]phenoxy}propionic Acids: A New Class of Dual PPARα/γ Agonists

2-Alkoxydihydrocinnamates as PPAR agonists. Activity modulation by the incorporation of phenoxy substituents

Asymmetric total synthesis of dibenzocyclooctadiene lignans (-)-schizandrin and (-)-isoschizandrin. Structure revision of (+)-isoschizandrin

Design and synthesis of novel and potent amide linked PPARγ/δ dual agonists

Tetrahydroisoquinoline PPARγ agonists: Design of novel, highly selective non-TZD antihyperglycemic agents

Synthesis and evaluation of aminomethyl dihydrocinnamates as a new class of PPAR ligands

Inhibition of thrombin activatable fibrinolysis inhibitor by cysteine derivatives

Discovery and characterization of [(cyclopentyl)ethyl]benzoic acid inhibitors of microsomal prostaglandin E synthase-1

Characterization of 3,3-dimethyl substituted N-aryl piperidines as potent microsomal prostaglandin E synthase-1 inhibitors

Synthesis of N,N‘-Orthogonally Protected (S)-Piperazine-2-carboxylic Acid

A Peroxisome Proliferator-Activated Receptor α/γ Dual Agonist with a Unique in Vitro Profile and Potent Glucose and Lipid Effects in Rodent Models of Type 2 Diabetes and Dyslipidemia

An approach toward the ophiobolane sesterterpenes: synthesis of the ceroplastin nucleus

Peroxisome Proliferator‐Activated Receptor γ Modulation for the Treatment of Type 2 Diabetes

Tetrahydroisoquinoline PPARgamma agonists: design of novel, highly selective non-TZD antihyperglycemic agents

Tetrahydroisoquinoline PPARrγ agonists : Design of novel, highly selective non-TZD antihyperglycemic agents

The synthesis of aminobenzazepinones as anti-phenylalanine dipeptide mimics and their use in nep inhibition

Design and synthesis of novel and potent amide linked PPARgamma/delta dual agonists

Suchergebnisse filtern