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Asymmetric synthesis and histamine receptor activity of new H1-receptor agonists and conformationally restricted H3-receptor antagonists

URN to cite this document: urn:nbn:de:bvb:355-opus-6673

Patil, Rameshwar (2007) Asymmetric synthesis and histamine receptor activity of new H1-receptor agonists and conformationally restricted H3-receptor antagonists. PhD, Universität Regensburg

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Abstract (English)

Histamine H1-Receptor (H1R) Ligands: Developing highly potent and selective histamine H1-receptor (H1R) agonists has been an arduous task for several decades. Highly potent and selective H1R agonists are in demand for pharmacological and molecular investigation. Recently, the histaprodifens, a family of 2-(3,3-diphenylpropyl)-substituted histamine derivatives, have been established as new class ...

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Translation of the abstract (German)

Histamin H1-Rezeptor (H1R) Liganden: Die Entwicklung hoch potenter und selektiver H1-Rezeptor (H1R) Agonisten war lange Zeit eine sehr schwierige Aufgabe. Vor kurzem konnten die Histaprodifene, eine Familie von 2-(3,3-Diphenylpropyl)-substituierten Histamin-Derivaten, als neuartige selektive und potente H1R Agonisten identifiziert werden. Auf der Basis dieser neuen Ergebnisse wurden in der ...

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Export bibliographical data

Item Type:Thesis of the University of Regensburg (PhD)
Date:12 June 2007
Referee:Oliver (Prof. Dr.) Reiser
Date of exam:30 May 2006
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser
Keywords:Histamin , Histaminanaloga , Asymmetrische Synthese , Aminohydroxylierung , Agonist , Antagonist , Histaminrezeptor , Histaminderivate , H3-Rezeptor , Histaprodifen , histamine , asymmetric synthesis , aminohydroxylation , agonist , antagonist , histaprodifen
Subjects:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Owner: Universitätsbibliothek Regensburg
Deposited On:27 Oct 2009 08:10
Last Modified:13 Mar 2014 11:43
Item ID:10500
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