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New 1,8-naphthyridine and quinoline derivatives as CB2 selective agonists

Bioorganic & medicinal chemistry letters, 2007-12, Vol.17 (23), p.6505-6510

2007

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Cannabinoid CB2/CB1 Selectivity. Receptor Modeling and Automated Docking Analysis

Journal of medicinal chemistry, 2006-02, Vol.49 (3), p.984-994

2006

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Rational Design, Synthesis, and Pharmacological Properties of New 1,8-Naphthyridin-2(1H)-on-3-Carboxamide Derivatives as Highly Selective Cannabinoid-2 Receptor Agonists

Journal of medicinal chemistry, 2009-06, Vol.52 (12), p.3644-3651

2009

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Synthesis and biological evaluation of 1,8-naphthyridin-4(1 H)-on-3-carboxamide derivatives as new ligands of cannabinoid receptors

Bioorganic & medicinal chemistry, 2004-04, Vol.12 (8), p.1921-1933

2004

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1,8-Naphthyridin-4-one derivatives as new ligands of A2A adenosine receptors

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (20), p.4604-4610

2005

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Design, Synthesis, and Biological Evaluation of New 1,8-Naphthyridin-4(1 H )-on-3-carboxamide and Quinolin-4(1 H )-on-3-carboxamide Derivatives as CB 2 Selective Agonists

Journal of medicinal chemistry, 2006-10, Vol.49 (20), p.5947-5957

2006

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Design, Synthesis, and Biological Evaluation of New 1,8-Naphthyridin-4(1H)-on-3-carboxamide and Quinolin-4(1H)-on-3-carboxamide Derivatives as CB2 Selective Agonists

Journal of medicinal chemistry, 2006-10, Vol.49 (20), p.5947-5957

2006

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Synthesis and evaluation of antimycobacterial activity of 4-phenyl-1,8-naphthyridine derivatives

Farmaco (Società chimica italiana : 1989), 1998-12, Vol.53 (12), p.741-746

1998

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Pharmacokinetics of Tramadol and its Metabolites M1, M2 and M5 in Horses Following Intravenous, Immediate Release (Fasted/Fed) and Sustained Release Single Dose Administration

Journal of equine veterinary science, 2007-11, Vol.27 (11), p.481-488

2007

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Synthesis and antiplatelet activity of some 2,7-di( N-cycloamino)-3-phenyl-1,8-naphthyridine derivatives

Farmaco (Società chimica italiana : 1989), 2001-04, Vol.56 (4), p.311-318

2001

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Synthesis and β-blocking activity of (R,S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2,3-b]pyridine:potential antihypertensive agents – Part IX

European journal of medicinal chemistry, 2000-09, Vol.35 (9), p.815-826

2000

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4-[6-(Dansylamino)hexylamino]-7-methyl-2-phenyl-1,8-naphthyridine as a new potential fluorescent probe for studying A1-adenosine receptor

Farmaco (Società chimica italiana : 1989), 2002-10, Vol.57 (10), p.783-786

2002

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Synthesis and antiplatelet activity of some 3-phenyl-1,8-naphthyridine derivatives

Farmaco (Società chimica italiana : 1989), 2000-09, Vol.55 (9), p.603-610

2000

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Synthesis and evaluation of antihypertensive activity of 1,8-naphthyridine derivatives. Part X

European journal of medicinal chemistry, 2001-11, Vol.36 (11), p.925-934

2001

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Study on Affinity Profile toward Native Human and Bovine Adenosine Receptors of a Series of 1,8-Naphthyridine Derivatives

Journal of medicinal chemistry, 2004-06, Vol.47 (12), p.3019-3031

2004

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New 1,8-naphthyridine and quinoline derivatives as CB sub(2) selective agonists

Bioorganic & medicinal chemistry, 2007-12, Vol.17 (23), p.6505-6510

2007

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Synthesis and β-blocking activity of (R, S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2,3-b]pyridine: Identification of β3-Antagonists

Bioorganic & medicinal chemistry, 2003-11, Vol.11 (23), p.4921-4931

2003

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Synthesis of 1,8-naphthyridine derivatives: Potential antihypertensive agents — Part VII

European journal of medicinal chemistry, 1998, Vol.33 (5), p.383-397

1998

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A Novel Class of Highly Potent and Selective A1 Adenosine Antagonists: Structure−Affinity Profile of a Series of 1,8-Naphthyridine Derivatives

Journal of medicinal chemistry, 2000-07, Vol.43 (15), p.2814-2823

2000

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New 1,8-naphthyridine and quinoline derivatives as CB 2 selective agonists

Bioorganic & medicinal chemistry letters, 2007, Vol.17 (23), p.6505-6510

2007

Volltextzugriff (PDF)

1,8-Naphthyridin-4-one derivatives as new ligands of A sub(2A) adenosine receptors

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (20), p.4604-4610

2005

Volltextzugriff (PDF)

1,8-Naphthyridin-4-one derivatives as new ligands of A 2A adenosine receptors

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (20), p.4604-4610

2005

Volltextzugriff (PDF)

Synthesis and beta-blocking activity of (R,S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2,3-b]pyridine: identification of beta 3-antagonists

Bioorganic & medicinal chemistry, 2003-11, Vol.11 (23), p.4921-4931

2003

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Synthesis of 1,8-naphthyridine derivatives. Potential antihypertensive agents. 1

Journal of heterocyclic chemistry, 1986-03, Vol.23 (2), p.501-504

1986

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Synthesis of 1,8-naphthyridine derivatives: potential antihypertensive agents – Part VIII

European journal of medicinal chemistry, 1999-06, Vol.34 (6), p.505-513

1999

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New 1,8-naphthyridine and quinoline derivatives as CB2 selective agonists

Cannabinoid CB2/CB1 Selectivity. Receptor Modeling and Automated Docking Analysis

Rational Design, Synthesis, and Pharmacological Properties of New 1,8-Naphthyridin-2(1H)-on-3-Carboxamide Derivatives as Highly Selective Cannabinoid-2 Receptor Agonists

Synthesis and biological evaluation of 1,8-naphthyridin-4(1 H)-on-3-carboxamide derivatives as new ligands of cannabinoid receptors

1,8-Naphthyridin-4-one derivatives as new ligands of A2A adenosine receptors

Design, Synthesis, and Biological Evaluation of New 1,8-Naphthyridin-4(1 H )-on-3-carboxamide and Quinolin-4(1 H )-on-3-carboxamide Derivatives as CB 2 Selective Agonists

Design, Synthesis, and Biological Evaluation of New 1,8-Naphthyridin-4(1H)-on-3-carboxamide and Quinolin-4(1H)-on-3-carboxamide Derivatives as CB2 Selective Agonists

Synthesis and evaluation of antimycobacterial activity of 4-phenyl-1,8-naphthyridine derivatives

Pharmacokinetics of Tramadol and its Metabolites M1, M2 and M5 in Horses Following Intravenous, Immediate Release (Fasted/Fed) and Sustained Release Single Dose Administration

Synthesis and antiplatelet activity of some 2,7-di( N-cycloamino)-3-phenyl-1,8-naphthyridine derivatives

Synthesis and β-blocking activity of (R,S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2,3-b]pyridine:potential antihypertensive agents – Part IX

4-[6-(Dansylamino)hexylamino]-7-methyl-2-phenyl-1,8-naphthyridine as a new potential fluorescent probe for studying A1-adenosine receptor

Synthesis and antiplatelet activity of some 3-phenyl-1,8-naphthyridine derivatives

Synthesis and evaluation of antihypertensive activity of 1,8-naphthyridine derivatives. Part X

Study on Affinity Profile toward Native Human and Bovine Adenosine Receptors of a Series of 1,8-Naphthyridine Derivatives

New 1,8-naphthyridine and quinoline derivatives as CB sub(2) selective agonists

Synthesis and β-blocking activity of (R, S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2,3-b]pyridine: Identification of β3-Antagonists

Synthesis of 1,8-naphthyridine derivatives: Potential antihypertensive agents — Part VII

A Novel Class of Highly Potent and Selective A1 Adenosine Antagonists: Structure−Affinity Profile of a Series of 1,8-Naphthyridine Derivatives

New 1,8-naphthyridine and quinoline derivatives as CB 2 selective agonists

1,8-Naphthyridin-4-one derivatives as new ligands of A sub(2A) adenosine receptors

1,8-Naphthyridin-4-one derivatives as new ligands of A 2A adenosine receptors

Synthesis and beta-blocking activity of (R,S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2,3-b]pyridine: identification of beta 3-antagonists

Synthesis of 1,8-naphthyridine derivatives. Potential antihypertensive agents. 1

Synthesis of 1,8-naphthyridine derivatives: potential antihypertensive agents – Part VIII

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