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...

Bilastine: a new H1‐antihistamine with an optimal profile for updosing in urticaria

Journal of the European Academy of Dermatology and Venereology, 2017-09, Vol.31 (9), p.1447-1452

2017

Volltextzugriff (PDF)

Bilastine: a new H 1 -antihistamine with an optimal profile for updosing in urticaria

Journal of the European Academy of Dermatology and Venereology, 2017-09, Vol.31 (9), p.1447-1452

2017

Volltextzugriff (PDF)

Updosing of bilastine is effective in moderate to severe chronic spontaneous urticaria: A real‐life study

Allergy (Copenhagen), 2018-10, Vol.73 (10), p.2073-2075

2018

Volltextzugriff (PDF)

In vivo pharmacological characterisation of bilastine, a potent and selective histamine H1 receptor antagonist

Drugs in R&D, 2006, Vol.7 (4), p.219-231

2006

Volltextzugriff (PDF)

Syntheses and Binding Studies of New [(Aryl)(aryloxy)methyl]piperidine Derivatives and Related Compounds as Potential Antidepressant Drugs with High Affinity for Serotonin (5-HT) and Norepinephrine (NE) Transporters

Journal of medicinal chemistry, 2003-12, Vol.46 (25), p.5512-5532

2003

Volltextzugriff (PDF)

New 2-Piperazinylbenzimidazole Derivatives as 5-HT3 Antagonists. Synthesis and Pharmacological Evaluation

Journal of medicinal chemistry, 1997-02, Vol.40 (4), p.586-593

1997

Volltextzugriff (PDF)

Preclinical pharmacology of F-98214-TA, a novel potent serotonin and norepinephrine uptake inhibitor with antidepressant and anxiolytic properties

Psychopharmacologia, 2005-11, Vol.182 (3), p.400-413

2005

Volltextzugriff (PDF)

Structural, conformational and pharmacological study of some amides derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9β-amine as potential analgesics

Journal of molecular structure, 1999-05, Vol.482-483, p.425-430

1999

Volltextzugriff (PDF)

2,3-Dihydro-2-oxo-1H-benzimidazole-1-carboxamides with Selective Affinity for the 5-HT4 Receptor: Synthesis and Structure−Affinity and Structure−Activity Relationships of a New Series of Partial Agonist and Antagonist Derivatives

Journal of medicinal chemistry, 1999-07, Vol.42 (15), p.2870-2880

1999

Volltextzugriff (PDF)

New substituted benzamides as 5-HT4 receptor antagonists

European journal of medicinal chemistry, 1995, Vol.30 (7-8), p.651-654

1995

Volltextzugriff (PDF)

Synthesis and pharmacological characterization of a new benzoxazole derivative as a potent 5-HT3 receptor agonist

Bioorganic & medicinal chemistry, 2003-07, Vol.11 (13), p.2709-2714

2003

Volltextzugriff (PDF)

Synthesis and Structural, Conformational, Biochemical, and Pharmacological Study of New Compounds Derived from Tropane-3-spiro-4’(5’)-imidazoline as Potential 5-HT3 Receptor Antagonists

Journal of pharmaceutical sciences, 1995-01, Vol.84 (1), p.101-106

1995

Volltextzugriff (PDF)

Structural, conformational, biochemical, and pharmacological study of some amides derived from 3,7-dimethyl-3,7-diazabicyclo [3.3.1] nonan-9-amine as potential 5-HT3 receptor antagonists

Journal of molecular structure, 1995-12, Vol.372 (2-3), p.203-213

1995

Volltextzugriff (PDF)

Synthesis and histamine H1-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

European journal of medicinal chemistry, 1996, Vol.31 (10), p.813-818

1996

Volltextzugriff (PDF)

New (2-methoxyphenyl)piperazine derivatives as 5-HT1A receptor ligands with reduced α1-adrenergic activity. Synthesis and structure-affinity relationships

Journal of medicinal chemistry, 1995-04, Vol.38 (8), p.1273-1277

1995

Volltextzugriff (PDF)

Synthesis and pharmacology of isoquinuclidine derivatives as 5-HT3 ligands

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (2), p.189-192

2002

Volltextzugriff (PDF)

New 3-benzisothiazolyl and 3-benzisoxazolylpiperazine derivatives with atypical antipsychotic binding profile

European journal of medicinal chemistry, 2002-09, Vol.37 (9), p.721-730

2002

Volltextzugriff (PDF)

Synthesis and structural, conformational and pharmacological study of new esters derived from 3,7-dimethyl-3,7-diazabicyclo[3.3.1]nonan-9-ol

Journal of molecular structure, 1995, Vol.351, p.127-135

1995

Volltextzugriff (PDF)

Structural, conformational, theoretical and pharmacological study of some amides derived from 3,7-dimethyl-9-[( N-substituted)-4-chlorobenzamido]3,7-diazabicyclo[3.3.1]nonane-9-carboxamide

Journal of molecular structure, 1995, Vol.351, p.137-146

1995

Volltextzugriff (PDF)

Synthesis, structural, conformational and pharmacological study of new fentanyl derivatives of the camphidine system

Journal of heterocyclic chemistry, 1994-03, Vol.31 (2), p.313-318

1994

Volltextzugriff (PDF)

Preclinical pharmacology of bilastine, a new selective histamine H1 receptor antagonist: receptor selectivity and in vitro antihistaminic activity

Drugs in R&D, 2005, Vol.6 (6), p.371-384

2005

Volltextzugriff (PDF)

Benzimidazole-2-carboxylic acid amides and esters : a new structural class of 5-HT3 ligands

European journal of medicinal chemistry, 1999-05, Vol.34 (5), p.415-422

1999

Volltextzugriff (PDF)

2,3-Dihydro-2-oxo-1H-benzimidazole-1-carboxamides with selective affinity for the 5-HT(4) receptor: synthesis and structure-affinity and structure-activity relationships of a new series of partial agonist and antagonist derivatives

Journal of medicinal chemistry, 1999-07, Vol.42 (15), p.2870-2880

1999

Volltextzugriff (PDF)

Synthesis, and structural, conformational and pharmacological studies of new fentanyl derivatives of the norgranatane system

J. Chem. Soc., Perkin Trans. 2, 1992 (4), p.687-695

1992

Volltextzugriff (PDF)

New (2-methoxyphenyl)piperazine derivatives as 5-HT1A receptor ligands with reduced alpha 1-adrenergic activity. Synthesis and structure-affinity relationships

Journal of medicinal chemistry, 1995-04, Vol.38 (8), p.1273-1277

1995

Volltextzugriff (PDF)

1 – 25 von 50

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(38)

Publikationsform

Artikel
(50)

Sprache

Englisch
(50)

Erscheinungsjahr

n.n

Thema

Science & Technology
(22)
Life Sciences & Biomedicine
(15)
Biological And Medical Sciences
(14)
Medical Sciences
(14)
Pharmacology. Drug Treatments
(14)
Animals
(13)
Rats
(12)
Male
(11)
Neuropharmacology
(11)
Chemistry
(10)
Pharmacology & Pharmacy
(10)
Physical Sciences
(10)
Chemistry, Medicinal
(9)
Neurotransmitters. Neurotransmission. Receptors
(9)
Rats, Wistar
(9)
Serotoninergic System
(9)
Structure-Activity Relationship
(8)
Guinea Pigs
(6)
Chemistry, Organic
(5)
Chemistry, Physical
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Bilastine: a new H1‐antihistamine with an optimal profile for updosing in urticaria

Bilastine: a new H 1 -antihistamine with an optimal profile for updosing in urticaria

Updosing of bilastine is effective in moderate to severe chronic spontaneous urticaria: A real‐life study

In vivo pharmacological characterisation of bilastine, a potent and selective histamine H1 receptor antagonist

Syntheses and Binding Studies of New [(Aryl)(aryloxy)methyl]piperidine Derivatives and Related Compounds as Potential Antidepressant Drugs with High Affinity for Serotonin (5-HT) and Norepinephrine (NE) Transporters

New 2-Piperazinylbenzimidazole Derivatives as 5-HT3 Antagonists. Synthesis and Pharmacological Evaluation

Preclinical pharmacology of F-98214-TA, a novel potent serotonin and norepinephrine uptake inhibitor with antidepressant and anxiolytic properties

Structural, conformational and pharmacological study of some amides derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9β-amine as potential analgesics

2,3-Dihydro-2-oxo-1H-benzimidazole-1-carboxamides with Selective Affinity for the 5-HT4 Receptor: Synthesis and Structure−Affinity and Structure−Activity Relationships of a New Series of Partial Agonist and Antagonist Derivatives

New substituted benzamides as 5-HT4 receptor antagonists

Synthesis and pharmacological characterization of a new benzoxazole derivative as a potent 5-HT3 receptor agonist

Synthesis and Structural, Conformational, Biochemical, and Pharmacological Study of New Compounds Derived from Tropane-3-spiro-4’(5’)-imidazoline as Potential 5-HT3 Receptor Antagonists

Structural, conformational, biochemical, and pharmacological study of some amides derived from 3,7-dimethyl-3,7-diazabicyclo [3.3.1] nonan-9-amine as potential 5-HT3 receptor antagonists

Synthesis and histamine H1-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

New (2-methoxyphenyl)piperazine derivatives as 5-HT1A receptor ligands with reduced α1-adrenergic activity. Synthesis and structure-affinity relationships

Synthesis and pharmacology of isoquinuclidine derivatives as 5-HT3 ligands

New 3-benzisothiazolyl and 3-benzisoxazolylpiperazine derivatives with atypical antipsychotic binding profile

Synthesis and structural, conformational and pharmacological study of new esters derived from 3,7-dimethyl-3,7-diazabicyclo[3.3.1]nonan-9-ol

Structural, conformational, theoretical and pharmacological study of some amides derived from 3,7-dimethyl-9-[( N-substituted)-4-chlorobenzamido]3,7-diazabicyclo[3.3.1]nonane-9-carboxamide

Synthesis, structural, conformational and pharmacological study of new fentanyl derivatives of the camphidine system

Preclinical pharmacology of bilastine, a new selective histamine H1 receptor antagonist: receptor selectivity and in vitro antihistaminic activity

Benzimidazole-2-carboxylic acid amides and esters : a new structural class of 5-HT3 ligands

2,3-Dihydro-2-oxo-1H-benzimidazole-1-carboxamides with selective affinity for the 5-HT(4) receptor: synthesis and structure-affinity and structure-activity relationships of a new series of partial agonist and antagonist derivatives

Synthesis, and structural, conformational and pharmacological studies of new fentanyl derivatives of the norgranatane system

New (2-methoxyphenyl)piperazine derivatives as 5-HT1A receptor ligands with reduced alpha 1-adrenergic activity. Synthesis and structure-affinity relationships

Suchergebnisse filtern