Clobenpropit analogs as dual activity ligands for the histamine H3 and H4 receptors: Synthesis, pharmacological evaluation, and cross-target QSAR studies-Reference-Cited by-同舟云学术

Clobenpropit analogs as dual activity ligands for the histamine H3 and H4 receptors: Synthesis, pharmacological evaluation, and cross-target QSAR studies

Published:2009-06 Issue:11 Volume:17 Page:3987-3994
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Lim Herman D.,Istyastono Enade P.,van de Stolpe Andrea,Romeo Giuseppe,Gobbi Silvia,Schepers Marjo,Lahaye Roger,Menge Wiro M.B.P.,Zuiderveld Obbe P.,Jongejan Aldo,Smits Rogier A.,Bakker Remko A.,Haaksma Eric E.J.,Leurs Rob,de Esch Iwan J.P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference24 articles.

1. Auto-inhibition of brain histamine release mediated by a novel class (H3) of histamine receptor

2. Histamine H3receptor ligands break ground in a remarkable plethora of therapeutic areas

3. Genomics Meets Histamine Receptors: New Subtypes, New Receptors

4. The role of histamine H1 and H4 receptors in allergic inflammation: the search for new antihistamines

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