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...

Highly Potent, Stable, and Selective Dimeric Hetarylpropylguanidine-Type Histamine H2 Receptor Agonists

ACS omega, 2018-03, Vol.3 (3), p.2865-2882

2018

Volltextzugriff (PDF)

Synthesis and dual histamine H₁ and H₂ receptor antagonist activity of cyanoguanidine derivatives

Molecules (Basel, Switzerland), 2013-11, Vol.18 (11), p.14186-14202

2013

Volltextzugriff (PDF)

[3H]UR-DE257: Development of a Tritium-Labeled Squaramide-Type Selective Histamine H2 Receptor Antagonist

ChemMedChem, 2015-01, Vol.10 (1), p.83-93

2015

Volltextzugriff (PDF)

Structure‐Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands

ChemistryOpen (Weinheim), 2019-03, Vol.8 (3), p.285-297

2019

Volltextzugriff (PDF)

Multiple differences in agonist and antagonist pharmacology between human and guinea pig histamine H1-receptor

The Journal of pharmacology and experimental therapeutics, 2003-06, Vol.305 (3), p.1104

2003

Volltextzugriff (PDF)

The Bivalent Ligand Approach Leads to Highly Potent and Selective Acylguanidine-Type Histamine H2 Receptor Agonists

Journal of medicinal chemistry, 2012-02, Vol.55 (3), p.1147-1160

2012

Volltextzugriff (PDF)

Structure-activity relationships of histamine H2 receptor ligands

Mini reviews in medicinal chemistry, 2004-11, Vol.4 (9), p.941-954

2004

Volltextzugriff (PDF)

Inhibition of FLT3 and PDGFR tyrosine kinase activity by bis(benzo[ b]furan-2-yl)methanones

Bioorganic & medicinal chemistry, 2007-03, Vol.15 (5), p.2187-2197

2007

Volltextzugriff (PDF)

Structure-activity relationships of histamine H1-receptor agonists

Mini reviews in medicinal chemistry, 2004-11, Vol.4 (9), p.935-940

2004

Volltextzugriff (PDF)

Molecular Basis for the Selective Interaction of Synthetic Agonists with the Human Histamine H1-Receptor Compared with the Guinea Pig H1-Receptor

Molecular pharmacology, 2009-03, Vol.75 (3), p.454-465

2009

Volltextzugriff (PDF)

Design and biological evaluation of tetrahydro-β-carboline derivatives as highly potent histone deacetylase 6 (HDAC6) inhibitors

European journal of medicinal chemistry, 2018-05, Vol.152, p.329-357

2018

Volltextzugriff (PDF)

Marbostat-100 Defines a New Class of Potent and Selective Antiinflammatory and Antirheumatic Histone Deacetylase 6 Inhibitors

Journal of medicinal chemistry, 2018-04, Vol.61 (8), p.3454-3477

2018

Volltextzugriff (PDF)

Histaprodifens: Synthesis, Pharmacological in Vitro Evaluation, and Molecular Modeling of a New Class of Highly Active and Selective Histamine H1-Receptor Agonists

Journal of medicinal chemistry, 2000-03, Vol.43 (6), p.1071-1084

2000

Volltextzugriff (PDF)

Highly Potent, Stable, and Selective Dimeric Hetarylpropylguanidine-Type Histamine H 2 Receptor Agonists

ACS omega, 2018-03, Vol.3 (3), p.2865-2882

2018

Volltextzugriff (PDF)

Structural modifications in the distal, regulatory region of histamine H3 receptor antagonists leading to the identification of a potent anti-obesity agent

European journal of medicinal chemistry, 2021-03, Vol.213, p.113041, Article 113041

2021

Volltextzugriff (PDF)

Progress in the proxifan class: heterocyclic congeners as novel potent and selective histamine H3-receptor antagonists

European journal of pharmaceutical sciences, 2002-05, Vol.15 (4), p.367-378

2002

Volltextzugriff (PDF)

Synthesis and pharmacological activity of fluorescent histamine H2 receptor antagonists related to potentidine

Bioorganic & medicinal chemistry letters, 2003-05, Vol.13 (10), p.1717-1720

2003

Volltextzugriff (PDF)

Structural modifications in the distal, regulatory region of histamine H 3 receptor antagonists leading to the identification of a potent anti-obesity agent

European journal of medicinal chemistry, 2021-03, Vol.213, p.113041

2021

Volltextzugriff (PDF)

[ 3 H]UR‐DE257: Development of a Tritium‐Labeled Squaramide‐Type Selective Histamine H 2 Receptor Antagonist

ChemMedChem, 2015-01, Vol.10 (1), p.83-93

2015

Volltextzugriff (PDF)

NG‐Acylated Aminothiazolylpropylguanidines as Potent and Selective Histamine H2 Receptor Agonists

ChemMedChem, 2009-02, Vol.4 (2), p.232-240

2009

Volltextzugriff (PDF)

A series of novel aryl-methanone derivatives as inhibitors of FMS-like tyrosine kinase 3 (FLT3) in FLT3-ITD-positive acute myeloid leukemia

European journal of medicinal chemistry, 2020-05, Vol.193, p.112232, Article 112232

2020

Volltextzugriff (PDF)

2,4-Diaminopyrimidines as dual ligands at the histamine H 1 and H 4 receptor—H 1 /H 4 -receptor selectivity

Bioorganic & medicinal chemistry letters, 2016-01, Vol.26 (2), p.292-300

2016

Volltextzugriff (PDF)

N1-(3-cyclohexylbutanoyl)-N2-[3-(1H-imidazol-4-yl)propyl]guanidine (UR-AK57), a potent partial agonist for the human histamine H1- and H2-receptors

The Journal of pharmacology and experimental therapeutics, 2006-06, Vol.317 (3), p.1262

2006

Volltextzugriff (PDF)

3-Bromo-4-(1H-3-indolyl)-2,5-dihydro-1H-2,5-pyrroledione derivatives as new lead compounds for antibacterially active substances

European journal of medicinal chemistry, 2006-02, Vol.41 (2), p.176-191

2006

Volltextzugriff (PDF)

Effects of ginger constituents on the gastrointestinal tract: role of cholinergic M3 and serotonergic 5-HT3 and 5-HT4 receptors

Planta medica, 2011-07, Vol.77 (10), p.973

2011

Volltextzugriff (PDF)

1 – 25 von 144

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(130)
Mit Volltextzugriff
(136)

Publikationsform

Artikel
(144)

Sprache

Englisch
(139)
Deutsch
(7)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(42)
Life Sciences & Biomedicine
(40)
Pharmacology & Pharmacy
(39)
Animals
(38)
Chemistry, Medicinal
(32)
Biological And Medical Sciences
(26)
Guinea Pigs
(26)
Medical Sciences
(26)
Pharmacology. Drug Treatments
(26)
Structure-Activity Relationship
(24)
Humans
(22)
Histamine Agonists - Pharmacology
(19)
Chemistry
(17)
Neuropharmacology
(15)
Neurotransmitters. Neurotransmission. Receptors
(15)
Physical Sciences
(14)
Rats
(14)
Histamine
(13)
Histamine Agonists - Chemistry
(12)
In Vitro Techniques
(12)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Highly Potent, Stable, and Selective Dimeric Hetarylpropylguanidine-Type Histamine H2 Receptor Agonists

Synthesis and dual histamine H₁ and H₂ receptor antagonist activity of cyanoguanidine derivatives

[3H]UR-DE257: Development of a Tritium-Labeled Squaramide-Type Selective Histamine H2 Receptor Antagonist

Structure‐Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands

Multiple differences in agonist and antagonist pharmacology between human and guinea pig histamine H1-receptor

The Bivalent Ligand Approach Leads to Highly Potent and Selective Acylguanidine-Type Histamine H2 Receptor Agonists

Structure-activity relationships of histamine H2 receptor ligands

Inhibition of FLT3 and PDGFR tyrosine kinase activity by bis(benzo[ b]furan-2-yl)methanones

Structure-activity relationships of histamine H1-receptor agonists

Molecular Basis for the Selective Interaction of Synthetic Agonists with the Human Histamine H1-Receptor Compared with the Guinea Pig H1-Receptor

Design and biological evaluation of tetrahydro-β-carboline derivatives as highly potent histone deacetylase 6 (HDAC6) inhibitors

Marbostat-100 Defines a New Class of Potent and Selective Antiinflammatory and Antirheumatic Histone Deacetylase 6 Inhibitors

Histaprodifens: Synthesis, Pharmacological in Vitro Evaluation, and Molecular Modeling of a New Class of Highly Active and Selective Histamine H1-Receptor Agonists

Highly Potent, Stable, and Selective Dimeric Hetarylpropylguanidine-Type Histamine H 2 Receptor Agonists

Structural modifications in the distal, regulatory region of histamine H3 receptor antagonists leading to the identification of a potent anti-obesity agent

Progress in the proxifan class: heterocyclic congeners as novel potent and selective histamine H3-receptor antagonists

Synthesis and pharmacological activity of fluorescent histamine H2 receptor antagonists related to potentidine

Structural modifications in the distal, regulatory region of histamine H 3 receptor antagonists leading to the identification of a potent anti-obesity agent

[ 3 H]UR‐DE257: Development of a Tritium‐Labeled Squaramide‐Type Selective Histamine H 2 Receptor Antagonist

NG‐Acylated Aminothiazolylpropylguanidines as Potent and Selective Histamine H2 Receptor Agonists

A series of novel aryl-methanone derivatives as inhibitors of FMS-like tyrosine kinase 3 (FLT3) in FLT3-ITD-positive acute myeloid leukemia

2,4-Diaminopyrimidines as dual ligands at the histamine H 1 and H 4 receptor—H 1 /H 4 -receptor selectivity

N1-(3-cyclohexylbutanoyl)-N2-[3-(1H-imidazol-4-yl)propyl]guanidine (UR-AK57), a potent partial agonist for the human histamine H1- and H2-receptors

3-Bromo-4-(1H-3-indolyl)-2,5-dihydro-1H-2,5-pyrroledione derivatives as new lead compounds for antibacterially active substances

Effects of ginger constituents on the gastrointestinal tract: role of cholinergic M3 and serotonergic 5-HT3 and 5-HT4 receptors

Suchergebnisse filtern