UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 32

Sortiert nach

Antidepressant-Like Activity and Modulation of Brain Monoaminergic Transmission by Blockade of Anandamide Hydrolysis

Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (51), p.18620-18625

2005

Volltextzugriff (PDF)

An endocannabinoid mechanism for stress-induced analgesia

Nature, 2005-06, Vol.435 (7045), p.1108-1112

2005

Volltextzugriff (PDF)

Changes in some biological parameters in 2 groups of animals exposed to experimental hypoxia, of which 1 group was simultaneously perfused with perhydrol

Bollettino della Societa italiana di biologia sperimentale, 1975-06, Vol.51 (12), p.728

1975

Volltextzugriff (PDF)

Survival time in 2 groups of 2 groups of animals, including one group in experimental hypoxia, and the other in the same conditions but perfused with perhydrol

Bollettino della Societa italiana di biologia sperimentale, 1975-06, Vol.51 (12), p.735

1975

Volltextzugriff (PDF)

Oleylethanolamide regulates feeding and body weight through activation of the nuclear receptor PPAR-α

Nature, 2003-09, Vol.425 (6953), p.90-93

2003

Volltextzugriff (PDF)

The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3'-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice

The Journal of pharmacology and experimental therapeutics, 2007-07, Vol.322 (1), p.236

2007

Volltextzugriff (PDF)

Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism

Nature neuroscience, 2010-10, Vol.13 (10), p.1265-1270

2010

Volltextzugriff (PDF)

Pharmacological characterization of hydrolysis-resistant analogs of oleoylethanolamide with potent anorexiant properties

The Journal of pharmacology and experimental therapeutics, 2006-08, Vol.318 (2), p.563

2006

Volltextzugriff (PDF)

A Second Generation of Carbamate-Based Fatty Acid Amide Hydrolase Inhibitors with Improved Activity in vivo

ChemMedChem, 2009-09, Vol.4 (9), p.1505-1513

2009

Volltextzugriff (PDF)

Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: Steric effects of N-alkyl chain on rat plasma and liver stability

European journal of medicinal chemistry, 2011-09, Vol.46 (9), p.4466-4473

2011

Volltextzugriff (PDF)

Structure–Property Relationships of a Class of Carbamate‐Based Fatty Acid Amide Hydrolase (FAAH) Inhibitors: Chemical and Biological Stability

ChemMedChem, 2009-09, Vol.4 (9), p.1495-1504

2009

Volltextzugriff (PDF)

The fatty-acid amide hydrolase inhibitor URB597 does not affect triacylglycerol hydrolysis in rat tissues

Pharmacological research, 2006-11, Vol.54 (5), p.341-344

2006

Volltextzugriff (PDF)

Melatonin Receptor Ligands: Synthesis of New Melatonin Derivatives and Comprehensive Comparative Molecular Field Analysis (CoMFA) Study

Journal of medicinal chemistry, 1998-09, Vol.41 (20), p.3831-3844

1998

Volltextzugriff (PDF)

2-[N-Acylamino(C1−C3)alkyl]indoles as MT1 Melatonin Receptor Partial Agonists, Antagonists, and Putative Inverse Agonists

Journal of medicinal chemistry, 1998-09, Vol.41 (19), p.3624-3634

1998

Volltextzugriff (PDF)

Synthesis, pharmacological characterization and QSAR studies on 2-substituted indole melatonin receptor ligands

Bioorganic & medicinal chemistry, 2001-04, Vol.9 (4), p.1045-1057

2001

Volltextzugriff (PDF)

2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists: further characterization of 3,5-Dimethyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-Trimethyl-propyl) ester and structure–Activity relationships

Bioorganic & medicinal chemistry letters, 2003-07, Vol.13 (13), p.2113-2118

2003

Volltextzugriff (PDF)

Synthesis and SAR of New 5-Phenyl-3-ureido-1,5-benzodiazepines as Cholecystokinin-B Receptor Antagonists

Journal of medicinal chemistry, 2000-10, Vol.43 (20), p.3596-3613

2000

Volltextzugriff (PDF)

Conformationally Restrained Melatonin Analogues: Synthesis, Binding Affinity for the Melatonin Receptor, Evaluation of the Biological Activity, and Molecular Modeling Study

Journal of medicinal chemistry, 1997-06, Vol.40 (13), p.1990-2002

1997

Volltextzugriff (PDF)

Pharmacological Profile of the Selective FAAH Inhibitor KDS‐4103 (URB597)

CNS drug reviews, 2006-03, Vol.12 (1), p.21-38

2006

Volltextzugriff (PDF)

1-(2-Alkanamidoethyl)-6-methoxyindole Derivatives: A New Class of Potent Indole Melatonin Analogues

Journal of medicinal chemistry, 1997-06, Vol.40 (13), p.2003-2010

1997

Volltextzugriff (PDF)

A new melatonin receptor ligand with mt1-agonist and MT2-antagonist properties

Journal of pineal research, 2000-11, Vol.29 (4), p.234-240

2000

Volltextzugriff (PDF)

(E)-3-(2-(N-Phenylcarbamoyl)vinyl)pyrrole-2-carboxylic Acid Derivatives. A Novel Class of Glycine Site Antagonists

Journal of medicinal chemistry, 1998-03, Vol.41 (6), p.808-820

1998

Volltextzugriff (PDF)

URB602 Inhibits Monoacylglycerol Lipase and Selectively Blocks 2-Arachidonoylglycerol Degradation in Intact Brain Slices

Chemistry & biology, 2007-12, Vol.14 (12), p.1357-1365

2007

Volltextzugriff (PDF)

3-(2-Carbamoylvinyl)-4,5-dimethylpyrrole-2-carboxylic acids as ligands at the NMDA glycine-binding site: a study on the 2-carbamoylvinyl chain modification

Farmaco (Società chimica italiana : 1989), 1999, Vol.54 (1), p.101-111

1999

Volltextzugriff (PDF)

DECHLORO TEICOPLANIN ANTIBIOTICS

The Journal of Antibiotics, 1989/11/25, Vol.42(11), pp.1684-1697

1989

Volltextzugriff (PDF)

1 – 25 von 32

Suche als RSS-Feed

Aktive Filter

ThemaAnimals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(28)
Mit Volltextzugriff
(26)

Publikationsform

Artikel
(32)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(25)
Life Sciences & Biomedicine
(22)
Pharmacology & Pharmacy
(20)
Rats
(17)
Male
(15)
Biological And Medical Sciences
(14)
Mice
(13)
Chemistry, Medicinal
(12)
Medical Sciences
(12)
Pharmacology. Drug Treatments
(12)
Structure-Activity Relationship
(12)
Carbamates - Pharmacology
(7)
Enzyme Inhibitors - Pharmacology
(7)
Humans
(7)
Rats, Wistar
(7)
Amidohydrolases - Antagonists & Inhibitors
(6)
In Vitro Techniques
(6)
Indoles - Pharmacology
(6)
Ligands
(6)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Antidepressant-Like Activity and Modulation of Brain Monoaminergic Transmission by Blockade of Anandamide Hydrolysis

An endocannabinoid mechanism for stress-induced analgesia

Changes in some biological parameters in 2 groups of animals exposed to experimental hypoxia, of which 1 group was simultaneously perfused with perhydrol

Survival time in 2 groups of 2 groups of animals, including one group in experimental hypoxia, and the other in the same conditions but perfused with perhydrol

Oleylethanolamide regulates feeding and body weight through activation of the nuclear receptor PPAR-α

The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3'-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice

Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism

Pharmacological characterization of hydrolysis-resistant analogs of oleoylethanolamide with potent anorexiant properties

A Second Generation of Carbamate-Based Fatty Acid Amide Hydrolase Inhibitors with Improved Activity in vivo

Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: Steric effects of N-alkyl chain on rat plasma and liver stability

Structure–Property Relationships of a Class of Carbamate‐Based Fatty Acid Amide Hydrolase (FAAH) Inhibitors: Chemical and Biological Stability

The fatty-acid amide hydrolase inhibitor URB597 does not affect triacylglycerol hydrolysis in rat tissues

Melatonin Receptor Ligands: Synthesis of New Melatonin Derivatives and Comprehensive Comparative Molecular Field Analysis (CoMFA) Study

2-[N-Acylamino(C1−C3)alkyl]indoles as MT1 Melatonin Receptor Partial Agonists, Antagonists, and Putative Inverse Agonists

Synthesis, pharmacological characterization and QSAR studies on 2-substituted indole melatonin receptor ligands

2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists: further characterization of 3,5-Dimethyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-Trimethyl-propyl) ester and structure–Activity relationships

Synthesis and SAR of New 5-Phenyl-3-ureido-1,5-benzodiazepines as Cholecystokinin-B Receptor Antagonists

Conformationally Restrained Melatonin Analogues: Synthesis, Binding Affinity for the Melatonin Receptor, Evaluation of the Biological Activity, and Molecular Modeling Study

Pharmacological Profile of the Selective FAAH Inhibitor KDS‐4103 (URB597)

1-(2-Alkanamidoethyl)-6-methoxyindole Derivatives: A New Class of Potent Indole Melatonin Analogues

A new melatonin receptor ligand with mt1-agonist and MT2-antagonist properties

(E)-3-(2-(N-Phenylcarbamoyl)vinyl)pyrrole-2-carboxylic Acid Derivatives. A Novel Class of Glycine Site Antagonists

URB602 Inhibits Monoacylglycerol Lipase and Selectively Blocks 2-Arachidonoylglycerol Degradation in Intact Brain Slices

3-(2-Carbamoylvinyl)-4,5-dimethylpyrrole-2-carboxylic acids as ligands at the NMDA glycine-binding site: a study on the 2-carbamoylvinyl chain modification

DECHLORO TEICOPLANIN ANTIBIOTICS

Aktive Filter

Suchergebnisse filtern