Hochschulschrift
Hetarylalkyl(aryl)cyanoguanidines as histamine H4 receptor ligands : synthesis, chiral separation, pharmacological characterization, structure-activity and -selectivity relationships
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Dimensions
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21 cm
- Extent
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X, 261 S.
- Language
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Englisch
- Notes
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graph. Darst.
Regensburg, Univ., Diss., 2011
- Classification
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Medizin, Gesundheit
Chemie
- Creator
- Table of contents
- Rights
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
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11.06.2025, 2:01 PM CEST
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Object type
- Hochschulschrift
Associated
Other Objects (12)
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Structural insights into the agonists binding and receptor selectivity of human histamine H4 receptor
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Functional analysis of the mouse histamine H4 receptor in myeloid cells
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Highly potent, selective acylguanidine type histamine H2-receptor agonists : synthesis and structure-activity relationships
Structure‐Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands †
Molecular characterization of RFamide peptide receptors : structure-activity relationships and functional selectivity
Hetarylalkyl(aryl)cyanoguanidines as histamine H4 receptor ligands: Synthesis, chiral separation, pharmacological characterization, structure-activity and -selectivity relationships
Structural insights into the agonists binding and receptor selectivity of human histamine H4 receptor
Aryl-1,3,5-triazine ligands of histamine H4 receptor attenuate inflammatory and nociceptive response to carrageen, zymosan and lipopolysaccharide
Functional analysis of the mouse histamine H4 receptor in myeloid cells
Basal Histamine H4 Receptor Activation: Agonist Mimicry by the Diphenylalanine Motif
Histamine H1- and H4-receptor expression in human colon-derived cell lines
Enantioselective synthesis of tetrahydrofuran-imidazole based human histamine H3 and H4 receptor agonists
Structural basis of ligand recognition and design of antihistamines targeting histamine H4 receptor
Enantioselective synthesis of tetrahydrofuran-imidazole based human histamine H3 and H4 receptor agonists
Highly potent, selective acylguanidine type histamine H2-receptor agonists : synthesis and structure-activity relationships
Structure‐Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands †
Molecular characterization of RFamide peptide receptors : structure-activity relationships and functional selectivity
Hetarylalkyl(aryl)cyanoguanidines as histamine H4 receptor ligands: Synthesis, chiral separation, pharmacological characterization, structure-activity and -selectivity relationships
Structural insights into the agonists binding and receptor selectivity of human histamine H4 receptor
Aryl-1,3,5-triazine ligands of histamine H4 receptor attenuate inflammatory and nociceptive response to carrageen, zymosan and lipopolysaccharide
Functional analysis of the mouse histamine H4 receptor in myeloid cells
Basal Histamine H4 Receptor Activation: Agonist Mimicry by the Diphenylalanine Motif
Histamine H1- and H4-receptor expression in human colon-derived cell lines
Enantioselective synthesis of tetrahydrofuran-imidazole based human histamine H3 and H4 receptor agonists
Structural basis of ligand recognition and design of antihistamines targeting histamine H4 receptor
Enantioselective synthesis of tetrahydrofuran-imidazole based human histamine H3 and H4 receptor agonists
Highly potent, selective acylguanidine type histamine H2-receptor agonists : synthesis and structure-activity relationships
Structure‐Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands †