Literature DB >> 22447158

Synthesis of 3-alkyl enol mimics inhibitors of type II dehydroquinase: factors influencing their inhibition potency.

Beatriz Blanco1, Antía Sedes, Antonio Peón, Heather Lamb, Alastair R Hawkins, Luis Castedo, Concepción González-Bello.   

Abstract

Several 3-alkylaryl mimics of the enol intermediate in the reaction catalyzed by type II dehydroquinase were synthesized to investigate the effect on the inhibition potency of replacing the oxygen atom in the side chain by a carbon atom. The length and the rigidity of the spacer was also studied. The inhibitory properties of the reported compounds against type II dehydroquinase from Mycobacterium tuberculosis and Helicobacter pylori are also reported. The binding modes of these analogs in the active site of both enzymes were studied by molecular docking using GOLD 5.0 and dynamic simulations studies.

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Year:  2012        PMID: 22447158     DOI: 10.1039/c2ob07081b

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Resistance in tuberculosis: what do we know and where can we go?

Authors:  Keith D Green; Sylvie Garneau-Tsodikova
Journal:  Front Microbiol       Date:  2013-07-23       Impact factor: 5.640

2.  Unraveling the kinetic diversity of microbial 3-dehydroquinate dehydratases of shikimate pathway.

Authors:  Chang Liu; Yi-Ming Liu; Qing-Lan Sun; Cheng-Ying Jiang; Shuang-Jiang Liu
Journal:  AMB Express       Date:  2015-02-01       Impact factor: 3.298

3.  QM/MM simulations identify the determinants of catalytic activity differences between type II dehydroquinase enzymes.

Authors:  Emilio Lence; Marc W van der Kamp; Concepción González-Bello; Adrian J Mulholland
Journal:  Org Biomol Chem       Date:  2018-06-20       Impact factor: 3.876

  3 in total

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