UB Paderborn / Katalog / Suche / in CDI

Discovery of Vibegron: A Potent and Selective β3 Adrenergic Receptor Agonist for the Treatment of Overactive Bladder

Journal of medicinal chemistry, 2016-01, Vol.59 (2), p.609-623

2016

Volltextzugriff (PDF)

Ruthenium-Catalyzed Carboxylative Cyclization of 1,6-Diynes

Journal of the American Chemical Society, 2007-02, Vol.129 (5), p.1030-1031

2007

Volltextzugriff (PDF)

Design, Synthesis, and Evaluation of Conformationally Restricted Acetanilides as Potent and Selective β3 Adrenergic Receptor Agonists for the Treatment of Overactive Bladder

Journal of medicinal chemistry, 2014-02, Vol.57 (4), p.1437-1453

2014

Volltextzugriff (PDF)

Investigation of piperazine benzamides as human β3 adrenergic receptor agonists for the treatment of overactive bladder

Bioorganic & medicinal chemistry letters, 2017-02, Vol.27 (4), p.1094-1098

2017

Volltextzugriff (PDF)

Investigation of piperazine benzamides as human β 3 adrenergic receptor agonists for the treatment of overactive bladder

Bioorganic & medicinal chemistry letters, 2017-02, Vol.27 (4), p.1094-1098

2017

Volltextzugriff (PDF)

Discovery and optimization of novel 4-[(aminocarbonyl)amino]- N-[4-(2-aminoethyl)phenyl]benzenesulfonamide ghrelin receptor antagonists

Bioorganic & medicinal chemistry letters, 2009-11, Vol.19 (21), p.6237-6240

2009

Volltextzugriff (PDF)

Discovery of a Potent and Orally Bioavailable CCR2 and CCR5 Dual Antagonist

ACS medicinal chemistry letters, 2010-04, Vol.1 (1), p.14-18

2010

Volltextzugriff (PDF)

Design, synthesis, and structure–activity relationship of novel CCR2 antagonists

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (6), p.1830-1834

2009

Volltextzugriff (PDF)

Heterocyclic acetamide and benzamide derivatives as potent and selective β3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

Bioorganic & medicinal chemistry letters, 2010-03, Vol.20 (6), p.1895-1899

2010

Volltextzugriff (PDF)

Potent heteroarylpiperidine and carboxyphenylpiperidine 1-alkyl-cyclopentane carboxamide CCR2 antagonists

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (3), p.994-998

2008

Volltextzugriff (PDF)

Conformational studies of 3-amino-1-alkyl-cyclopentane carboxamide CCR2 antagonists leading to new spirocyclic antagonists

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (4), p.1374-1377

2008

Volltextzugriff (PDF)

Heterocyclic acetamide and benzamide derivatives as potent and selective b sub(3)-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

Bioorganic & medicinal chemistry letters, 2010-03, Vol.20 (6), p.1895-1899

2010

Volltextzugriff (PDF)

Heterocyclic acetamide and benzamide derivatives as potent and selective β 3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (6), p.1895-1899

2010

Volltextzugriff (PDF)

Transition metal-catalyzed tandem carbon-oxygen and carbon-carbon bond forming reactions of alkynes in (1) the addition-cyclization of carboxylic acids with 1,6-diynes and in (2) the total synthesis of frondosin B

Goble, Stephen D

2006

Volltextzugriff (PDF)

Heterocyclic acetamide and benzamide derivatives as potent and selective beta3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

Bioorganic & medicinal chemistry letters, 2010-03, Vol.20 (6), p.1895-1899

2010

Volltextzugriff (PDF)

Ruthenium-Catalyzed Carboxylative Cyclization of 1,6-Diynes

ChemInform, 2007-06, Vol.38 (24), p.no-no

2007

Volltextzugriff (PDF)

Proteinase 3 promotes formation of multinucleated giant cells and granuloma-like structures in patients with granulomatosis with polyangiitis

Annals of the rheumatic diseases, 2023-06, Vol.82 (6), p.848

2023

Volltextzugriff (PDF)

Microscale High-Throughput Experimentation as an Enabling Technology in Drug Discovery: Application in the Discovery of (Piperidinyl)pyridinyl‑1H‑benzimidazole Diacylglycerol Acyltransferase 1 Inhibitors

Journal of medicinal chemistry, 2017-05, Vol.60 (9), p.3594-3605

2017

Volltextzugriff (PDF)

Sequencing and analysis of the genome of the Whipple's disease bacterium Tropheryma whipplei

The Lancet (British edition), 2003-02, Vol.361 (9358), p.637-644

2003

Volltextzugriff (PDF)

Data Management in Computational Systems Biology: Exploring Standards, Tools, Databases, and Packaging Best Practices

Methods in molecular biology (Clifton, N.J.), 2019, Vol.2049, p.285

2019

Volltextzugriff (PDF)

Comparative analysis of the genome sequences of Bordetella pertussis , Bordetella parapertussis and Bordetella bronchiseptica

Nature genetics, 2003-09, Vol.35 (1), p.32-40

2003

Volltextzugriff (PDF)

Microscale High-Throughput Experimentation as an Enabling Technology in Drug Discovery: Application in the Discovery of (Piperidinyl)pyridinyl-1 H -benzimidazole Diacylglycerol Acyltransferase 1 Inhibitors

Journal of medicinal chemistry, 2017-05, Vol.60 (9), p.3594-3605

2017

Volltextzugriff (PDF)

ISPIDER Central: an integrated database web-server for proteomics

Nucleic acids research, 2008-07, Vol.36 (Web Server issue), p.W485

2008

Volltextzugriff (PDF)

Menü

Weitere Dienste

Einstellungen

Discovery of Vibegron: A Potent and Selective β3 Adrenergic Receptor Agonist for the Treatment of Overactive Bladder

Ruthenium-Catalyzed Carboxylative Cyclization of 1,6-Diynes

Design, Synthesis, and Evaluation of Conformationally Restricted Acetanilides as Potent and Selective β3 Adrenergic Receptor Agonists for the Treatment of Overactive Bladder

Investigation of piperazine benzamides as human β3 adrenergic receptor agonists for the treatment of overactive bladder

Investigation of piperazine benzamides as human β 3 adrenergic receptor agonists for the treatment of overactive bladder

Discovery and optimization of novel 4-[(aminocarbonyl)amino]- N-[4-(2-aminoethyl)phenyl]benzenesulfonamide ghrelin receptor antagonists

Discovery of a Potent and Orally Bioavailable CCR2 and CCR5 Dual Antagonist

Design, synthesis, and structure–activity relationship of novel CCR2 antagonists

Heterocyclic acetamide and benzamide derivatives as potent and selective β3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

Potent heteroarylpiperidine and carboxyphenylpiperidine 1-alkyl-cyclopentane carboxamide CCR2 antagonists

Conformational studies of 3-amino-1-alkyl-cyclopentane carboxamide CCR2 antagonists leading to new spirocyclic antagonists

Discovery of Vibegron: A Potent and Selective β 3 Adrenergic Receptor Agonist for the Treatment of Overactive Bladder

Design, Synthesis, and Evaluation of Conformationally Restricted Acetanilides as Potent and Selective β 3 Adrenergic Receptor Agonists for the Treatment of Overactive Bladder

Heterocyclic acetamide and benzamide derivatives as potent and selective b sub(3)-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

Heterocyclic acetamide and benzamide derivatives as potent and selective β 3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

Transition metal-catalyzed tandem carbon-oxygen and carbon-carbon bond forming reactions of alkynes in (1) the addition-cyclization of carboxylic acids with 1,6-diynes and in (2) the total synthesis of frondosin B

Heterocyclic acetamide and benzamide derivatives as potent and selective beta3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

Ruthenium-Catalyzed Carboxylative Cyclization of 1,6-Diynes

Proteinase 3 promotes formation of multinucleated giant cells and granuloma-like structures in patients with granulomatosis with polyangiitis

Microscale High-Throughput Experimentation as an Enabling Technology in Drug Discovery: Application in the Discovery of (Piperidinyl)pyridinyl‑1H‑benzimidazole Diacylglycerol Acyltransferase 1 Inhibitors

Sequencing and analysis of the genome of the Whipple's disease bacterium Tropheryma whipplei

Data Management in Computational Systems Biology: Exploring Standards, Tools, Databases, and Packaging Best Practices

Comparative analysis of the genome sequences of Bordetella pertussis , Bordetella parapertussis and Bordetella bronchiseptica

Microscale High-Throughput Experimentation as an Enabling Technology in Drug Discovery: Application in the Discovery of (Piperidinyl)pyridinyl-1 H -benzimidazole Diacylglycerol Acyltransferase 1 Inhibitors

ISPIDER Central: an integrated database web-server for proteomics

Suchergebnisse filtern