Literature DB >> 15225734

Structure-activity relationships of a novel series of melanin-concentrating hormone (MCH) receptor antagonists.

Rosa Arienzo1, David E Clark, Sue Cramp, Stephen Daly, Hazel J Dyke, Peter Lockey, Dennis Norman, Alan G Roach, Keith Stuttle, Maxine Tomlinson, Melanie Wong, Stephen P Wren.   

Abstract

A new series of 2-aminoquinolines has been identified as antagonists of the melanin concentrating hormone receptor (MCH-1R). Syntheses and structure-activity relationships are described leading to a compound having low nanomolar activity against the receptor and demonstrating functional antagonism. Studies also showed that some of the compounds were selective against a range of other G protein-coupled receptors.

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Year:  2004        PMID: 15225734     DOI: 10.1016/j.bmcl.2004.05.051

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

Review 1.  Advancements in the synthesis of fused tetracyclic quinoline derivatives.

Authors:  Ramadan A Mekheimer; Mariam A Al-Sheikh; Hanadi Y Medrasi; Kamal U Sadek
Journal:  RSC Adv       Date:  2020-05-27       Impact factor: 4.036

2.  A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines.

Authors:  Yerramsetti Nanaji; Seema Kirar; Sandip V Pawar; Ashok Kumar Yadav
Journal:  RSC Adv       Date:  2020-02-20       Impact factor: 4.036

3.  Tandem Cu-catalyzed ketenimine formation and intramolecular nucleophile capture: Synthesis of 1,2-dihydro-2-iminoquinolines from 1-(o-acetamidophenyl)propargyl alcohols.

Authors:  Gadi Ranjith Kumar; Yalla Kiran Kumar; Ruchir Kant; Maddi Sridhar Reddy
Journal:  Beilstein J Org Chem       Date:  2014-05-28       Impact factor: 2.883

  3 in total

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