Hochschulschrift
Enantioselective synthesis of tetrahydrofuran-imidazole based human histamine H3 and H4 receptor agonists
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Dimensions
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21 cm
- Extent
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161 S.
- Language
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Englisch
- Notes
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graph. Darst.
Regensburg, Univ., Diss., 2009
- Keyword
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Arzneimittelentwicklung
Arzneimitteldesign
- Creator
- URN
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urn:nbn:de:bvb:355-epub-134216
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:37 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
Other Objects (12)
Enantioselective synthesis of tetrahydrofuran-imidazole based human histamine H3 and H4 receptor agonists
Structural insights into the agonists binding and receptor selectivity of human histamine H4 receptor
Synthesis and pharmacological characterization of new tetrahydrofuran based compounds as histamine receptor ligands
Synthesis and pharmacological characterization of new tetrahydrofuran based compounds as histamine receptor ligands
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
Coordination Stoichiometry Effects on the Binding Hierarchy of Histamine and Imidazole–M 2+ Complexes
Structural basis of ligand recognition and design of antihistamines targeting histamine H4 receptor
Radioligand binding and reporter gene assays for histamine H3 and H4 receptor species orthologs
Pseudoreceptor-based pocket selection in a molecular dynamics simulation of the histamine H4 receptor
Radioligand binding and reporter gene assays for histamine H3 and H4 receptor species orthologs
Enantioselective synthesis of tetrahydrofuran-imidazole based human histamine H3 and H4 receptor agonists
Structural insights into the agonists binding and receptor selectivity of human histamine H4 receptor
Synthesis and pharmacological characterization of new tetrahydrofuran based compounds as histamine receptor ligands
Synthesis and pharmacological characterization of new tetrahydrofuran based compounds as histamine receptor ligands
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
Coordination Stoichiometry Effects on the Binding Hierarchy of Histamine and Imidazole–M 2+ Complexes
Structural basis of ligand recognition and design of antihistamines targeting histamine H4 receptor
Radioligand binding and reporter gene assays for histamine H3 and H4 receptor species orthologs
Pseudoreceptor-based pocket selection in a molecular dynamics simulation of the histamine H4 receptor
Radioligand binding and reporter gene assays for histamine H3 and H4 receptor species orthologs
Enantioselective synthesis of tetrahydrofuran-imidazole based human histamine H3 and H4 receptor agonists
Structural insights into the agonists binding and receptor selectivity of human histamine H4 receptor
Synthesis and pharmacological characterization of new tetrahydrofuran based compounds as histamine receptor ligands
Synthesis and pharmacological characterization of new tetrahydrofuran based compounds as histamine receptor ligands
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
Coordination Stoichiometry Effects on the Binding Hierarchy of Histamine and Imidazole–M 2+ Complexes
Structural basis of ligand recognition and design of antihistamines targeting histamine H4 receptor
Radioligand binding and reporter gene assays for histamine H3 and H4 receptor species orthologs
Pseudoreceptor-based pocket selection in a molecular dynamics simulation of the histamine H4 receptor