Literature DB >> 16644531

Synthesis and inhibitory activity of 8-substituted 2-deoxy-beta-KDO against CMP-KDO synthetase.

Hayamitsu Adachi1, Ken-Ichiro Kondo, Fukiko Kojima, Yoji Umezawa, Keiko Ishino, Kunimoto Hotta, Yoshio Nishimura.   

Abstract

3-Deoxy-D-manno-octulosonate cytidyltransferase (CMP-KDO synthetase) is involved in the biosynthesis of lipopolysaccharide (LPS) which is an essential component of the outer membrane of gram-negative bacteria. New CMP-KDO synthetase inhibitors, 8-substituted derivatives of 2-deoxy-beta-KDO (2) have been prepared. Compounds 8, 11, 15 and 16 in which the 8-hydroxyl group of 2 is replaced by guanidine, di(carbamoylethyl)amino, p-methoxy- or p-nitro-benzyloxycarbonylamino, respectively affect moderately the CMP-KDO synthetase activity.

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Year:  2006        PMID: 16644531     DOI: 10.1080/14756360500183699

Source DB:  PubMed          Journal:  Nat Prod Res        ISSN: 1478-6419            Impact factor:   2.861


  2 in total

1.  Enzymatic synthesis of 3-deoxy-d-manno-octulosonic acid (KDO) and its application for LPS assembly.

Authors:  Liuqing Wen; Yuan Zheng; Tiehai Li; Peng George Wang
Journal:  Bioorg Med Chem Lett       Date:  2016-04-21       Impact factor: 2.823

Review 2.  Antibiotics and bacterial resistance in the 21st century.

Authors:  Richard J Fair; Yitzhak Tor
Journal:  Perspect Medicin Chem       Date:  2014-08-28
  2 in total

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