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...

The pharmacology of TUG-891, a potent and selective agonist of the free fatty acid receptor 4 (FFA4/GPR120), demonstrates both potential opportunity and possible challenges to therapeutic agonism

Molecular pharmacology, 2013-11, Vol.84 (5), p.710-725

2013

Volltextzugriff (PDF)

Polyunsaturated fatty acid receptors, GPR40 and GPR120, are expressed in the hypothalamus and control energy homeostasis and inflammation

Journal of neuroinflammation, 2017-04, Vol.14 (1), p.91-91, Article 91

2017

Volltextzugriff (PDF)

Development and Characterization of a Potent Free Fatty Acid Receptor 1 (FFA1) Fluorescent Tracer

Journal of medicinal chemistry, 2016-05, Vol.59 (10), p.4849-4858

2016

Volltextzugriff (PDF)

Defining the Molecular Basis for the First Potent and Selective Orthosteric Agonists of the FFA2 Free Fatty Acid Receptor

The Journal of biological chemistry, 2013-06, Vol.288 (24), p.17296-17312

2013

Volltextzugriff (PDF)

Development and Characterization of a Fluorescent Tracer for the Free Fatty Acid Receptor 2 (FFA2/GPR43)

Journal of medicinal chemistry, 2017-07, Vol.60 (13), p.5638-5645

2017

Volltextzugriff (PDF)

Complex pharmacology of novel allosteric free fatty acid 3 receptor ligands

Molecular pharmacology, 2014-08, Vol.86 (2), p.200-210

2014

Volltextzugriff (PDF)

Dietary Fatty Acids and Their Potential for Controlling Metabolic Diseases Through Activation of FFA4 GPR120

Annual review of nutrition, 2015-07, Vol.35 (1), p.239-263

2015

Volltextzugriff (PDF)

Discovery of Potent and Selective Agonists for the Free Fatty Acid Receptor 1 (FFA1/GPR40), a Potential Target for the Treatment of Type II Diabetes

Journal of medicinal chemistry, 2008-11, Vol.51 (22), p.7061-7064

2008

Volltextzugriff (PDF)

Discovery of TUG-770: A Highly Potent Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist for Treatment of Type 2 Diabetes

ACS medicinal chemistry letters, 2013-05, Vol.4 (5), p.441-445

2013

Volltextzugriff (PDF)

Selective Orthosteric Free Fatty Acid Receptor 2 (FFA2) Agonists

The Journal of biological chemistry, 2011-03, Vol.286 (12), p.10628-10640

2011

Volltextzugriff (PDF)

A protocol for amide bond formation with electron deficient amines and sterically hindered substrates

Organic & biomolecular chemistry, 2016-01, Vol.14 (2), p.430-433

2016

Volltextzugriff (PDF)

Non-Acidic Free Fatty Acid Receptor 4 Agonists with Antidiabetic Activity

Journal of medicinal chemistry, 2016-10, Vol.59 (19), p.8868-8878

2016

Volltextzugriff (PDF)

Selective orthosteric free fatty acid receptor 2 (FFA2) agonists: identification of the structural and chemical requirements for selective activation of FFA2 versus FFA3

The Journal of biological chemistry, 2011-03, Vol.286 (12), p.10628-10640

2011

Volltextzugriff (PDF)

Identification of a Potent and Selective Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist with Favorable Physicochemical and in Vitro ADME Properties

Journal of medicinal chemistry, 2011-10, Vol.54 (19), p.6691-6703

2011

Volltextzugriff (PDF)

Discovery of potent and selective agonists for the free fatty acid receptor 1 (FFA(1)/GPR40), a potential target for the treatment of type II diabetes

Journal of medicinal chemistry, 2008-11, Vol.51 (22), p.7061-7064

2008

Volltextzugriff (PDF)

Discovery of a Potent and Selective Free Fatty Acid Receptor 1 Agonist with Low Lipophilicity and High Oral Bioavailability

Journal of medicinal chemistry, 2013-02, Vol.56 (3), p.982-992

2013

Volltextzugriff (PDF)

Conjugated Linoleic Acids Mediate Insulin Release through Islet G Protein-coupled Receptor FFA1/GPR40

The Journal of biological chemistry, 2011-04, Vol.286 (14), p.11890-11894

2011

Volltextzugriff (PDF)

Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonists: Mesylpropoxy Appendage Lowers Lipophilicity and Improves ADME Properties

Journal of medicinal chemistry, 2012-07, Vol.55 (14), p.6624-6628

2012

Volltextzugriff (PDF)

Discovery of a Potent Free Fatty Acid 1 Receptor Agonist with Low Lipophilicity, Low Polar Surface Area, and Robust in Vivo Efficacy

Journal of medicinal chemistry, 2016-03, Vol.59 (6), p.2841-2846

2016

Volltextzugriff (PDF)

A protocol for amide bond formation with electron deficient amines and sterically hindered substratesElectronic supplementary information (ESI) available: Synthetic procedures, compound characterization, NMR spectra. See DOI: 10.1039/c5ob02129d

2015-12

Volltextzugriff (PDF)

A Rapid and Efficient Sonogashira Protocol and Improved Synthesis of Free Fatty Acid 1 (FFA1) Receptor Agonists

Journal of organic chemistry, 2010-02, Vol.75 (4), p.1301-1304

2010

Volltextzugriff (PDF)

Gastrointestinal bleeding and intussusception caused by Peutz-Jeghers syndrome

Ugeskrift for læger, 2011-10, Vol.173 (44), p.2800

2011

Volltextzugriff (PDF)

Structure−Activity Study of Dihydrocinnamic Acids and Discovery of the Potent FFA1 (GPR40) Agonist TUG-469

ACS medicinal chemistry letters, 2010-10, Vol.1 (7), p.345-349

2010

Volltextzugriff (PDF)

ChemInform Abstract: A Protocol for Amide Bond Formation with Electron Deficient Amines and Sterically Hindered Substrates

ChemInform, 2016-04, Vol.47 (20), p.no-no

2016

Volltextzugriff (PDF)

Ada features and real-time embedded applications

ACM SIGAda Ada Letters, 1987-10, Vol.VII (6), p.116-118

Christiansen, Elisabeth Broe

1987

Volltextzugriff (PDF)

1 – 25 von 126

Suche als RSS-Feed

Aktive Filter

KollektionJournals@Ovid Ovid Full Text

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(106)
Mit Volltextzugriff
(115)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(78)
Life Sciences & Biomedicine
(61)
Humans
(44)
Female
(24)
Physical Sciences
(18)
Animals
(16)
Male
(16)
Astronomy & Astrophysics
(12)
Pharmacology & Pharmacy
(12)
Middle Aged
(11)
Receptors, G-Protein-Coupled - Agonists
(11)
Adult
(10)
Aged
(10)
Astronomy
(10)
Chemistry, Medicinal
(10)
Immunology
(10)
Extrasolar Planets
(9)
Transit
(9)
Mice
(8)
Structure-Activity Relationship
(8)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

The pharmacology of TUG-891, a potent and selective agonist of the free fatty acid receptor 4 (FFA4/GPR120), demonstrates both potential opportunity and possible challenges to therapeutic agonism

Polyunsaturated fatty acid receptors, GPR40 and GPR120, are expressed in the hypothalamus and control energy homeostasis and inflammation

Development and Characterization of a Potent Free Fatty Acid Receptor 1 (FFA1) Fluorescent Tracer

Defining the Molecular Basis for the First Potent and Selective Orthosteric Agonists of the FFA2 Free Fatty Acid Receptor

Development and Characterization of a Fluorescent Tracer for the Free Fatty Acid Receptor 2 (FFA2/GPR43)

Complex pharmacology of novel allosteric free fatty acid 3 receptor ligands

Dietary Fatty Acids and Their Potential for Controlling Metabolic Diseases Through Activation of FFA4 GPR120

Discovery of Potent and Selective Agonists for the Free Fatty Acid Receptor 1 (FFA1/GPR40), a Potential Target for the Treatment of Type II Diabetes

Discovery of TUG-770: A Highly Potent Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist for Treatment of Type 2 Diabetes

Selective Orthosteric Free Fatty Acid Receptor 2 (FFA2) Agonists

A protocol for amide bond formation with electron deficient amines and sterically hindered substrates

Non-Acidic Free Fatty Acid Receptor 4 Agonists with Antidiabetic Activity

Selective orthosteric free fatty acid receptor 2 (FFA2) agonists: identification of the structural and chemical requirements for selective activation of FFA2 versus FFA3

Identification of a Potent and Selective Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist with Favorable Physicochemical and in Vitro ADME Properties

Discovery of potent and selective agonists for the free fatty acid receptor 1 (FFA(1)/GPR40), a potential target for the treatment of type II diabetes

Discovery of a Potent and Selective Free Fatty Acid Receptor 1 Agonist with Low Lipophilicity and High Oral Bioavailability

Conjugated Linoleic Acids Mediate Insulin Release through Islet G Protein-coupled Receptor FFA1/GPR40

Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonists: Mesylpropoxy Appendage Lowers Lipophilicity and Improves ADME Properties

Discovery of a Potent Free Fatty Acid 1 Receptor Agonist with Low Lipophilicity, Low Polar Surface Area, and Robust in Vivo Efficacy

A protocol for amide bond formation with electron deficient amines and sterically hindered substratesElectronic supplementary information (ESI) available: Synthetic procedures, compound characterization, NMR spectra. See DOI: 10.1039/c5ob02129d

A Rapid and Efficient Sonogashira Protocol and Improved Synthesis of Free Fatty Acid 1 (FFA1) Receptor Agonists

Gastrointestinal bleeding and intussusception caused by Peutz-Jeghers syndrome

Structure−Activity Study of Dihydrocinnamic Acids and Discovery of the Potent FFA1 (GPR40) Agonist TUG-469

ChemInform Abstract: A Protocol for Amide Bond Formation with Electron Deficient Amines and Sterically Hindered Substrates

Ada features and real-time embedded applications

Aktive Filter

Suchergebnisse filtern