Literature DB >> 16762549

Substituted chromones and quinolones as potent melanin-concentrating hormone receptor 1 antagonists.

Brian Dyck1, Liren Zhao, Junko Tamiya, Joseph Pontillo, Sarah Hudson, Brett Ching, Christopher E Heise, Jenny Wen, Christi Norton, Ajay Madan, David Schwarz, Warren Wade, Val S Goodfellow.   

Abstract

A series of substituted chromones were designed, synthesized, and evaluated for their ability to bind melanin-concentrating hormone receptor 1. Compounds with subnanomolar binding affinity and 66% oral bioavailability in rats were discovered.

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Year:  2006        PMID: 16762549     DOI: 10.1016/j.bmcl.2006.05.075

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


  2 in total

1.  Fluorinated photoremovable protecting groups: the influence of fluoro substituents on the photo-Favorskii rearrangement.

Authors:  Kenneth F Stensrud; Dominik Heger; Peter Sebej; Jakob Wirz; Richard S Givens
Journal:  Photochem Photobiol Sci       Date:  2008-04-03       Impact factor: 3.982

2.  Synthesis of Palladium(II) Complexes via Michael Addition: Antiproliferative Effects through ROS-Mediated Mitochondrial Apoptosis and Docking with SARS-CoV-2.

Authors:  Jebiti Haribabu; Swaminathan Srividya; Dharmasivam Mahendiran; Dasararaju Gayathri; Vemula Venkatramu; Nattamai Bhuvanesh; Ramasamy Karvembu
Journal:  Inorg Chem       Date:  2020-11-24       Impact factor: 5.165

  2 in total

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