Literature DB >> 20580551

Synthesis and pharmacological evaluation of 1,1,3-substituted urea derivatives as potent TNF-alpha production inhibitors.

Hiroshi Enomoto1, Ayako Sawa, Hiroshi Suhara, Noriyoshi Yamamoto, Hiroyuki Inoue, Chikako Setoguchi, Fumio Tsuji, Masahiro Okamoto, Yoshimasa Sasabuchi, Masato Horiuchi, Masakazu Ban.   

Abstract

A three substituted urea derivative, SA13353 (compound 1a), exhibited potent inhibitory activity against lipopolysaccharide (LPS)-induced TNF-alpha production. We focused on the 1,1-substituted moiety (R(1) and R(2)) of SA13353 and investigated substituent effects of this moiety on LPS-induced TNF-alpha production by oral administration in rats. The synthesis of the urea derivatives was performed rapidly in a one-pot manner using a manual synthesizer. Several compounds containing hydrophobic substituents at this moiety showed more potent inhibitory activities than SA13353. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20580551     DOI: 10.1016/j.bmcl.2010.06.037

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


  2 in total

1.  (2SR,3RS)-Methyl 2-(adamantan-1-yl)-3-phenyl-sulfonyl-3-(pyridin-2-ylsulfan-yl)propano-ate dichloro-methane hemisolvate.

Authors:  Rosa-Luisa Meza-León; Sylvain Bernès; Elsie Ramírez Domínguez; Martha Sosa-Rivadeneyra; Leticia Quintero-Cortés
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-03-26

2.  In Silico Screening of IL-1β Production Inhibitors Using Chemometric Tools.

Authors:  Amirhossein Sakhteman; Najmeh Edraki; Bahram Hemmateenejad; Ramin Miri; Alireza Foroumadi; Abbas Shafiee; Mehdi Khoshneviszadeh
Journal:  Iran J Pharm Res       Date:  2017       Impact factor: 1.696

  2 in total

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