Mechanism and Inhibition of LpxC: An Essential Zinc-Dependent Deacetylase of Bacterial Lipid A Synthesis

Publisher： Bentham Science Publishers

E-ISSN： 1873-4316|9|1|9-15

ISSN： 1389-2010

Source： Current Pharmaceutical Biotechnology, Vol.9, Iss.1, 2008-02, pp. : 9-15

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

UDP-3-O-(R-3-hydroxymyristoyl)-N-Acetylglucosamine Deacetylase (LpxC) Inhibitors: A New Class of Antibacterial Agents

By  

Current Medicinal Chemistry, Vol. 19, Iss. 13, 2012-05 ,pp. : 2038-2050

Bentham Science Publishers

Access to resources Recommend Favorite

Recent Process in the Inhibitors of UDP-3-O-(R-3-hydroxyacyl)-Nacetylglucosamine Deacetylase (LpxC) Against Gram-Negative Bacteria

By  

Mini Reviews in Medicinal Chemistry, Vol. 18, Iss. 4, 2018-01 ,pp. : 310-323

Bentham Science Publishers

Access to resources Recommend Favorite

Mechanism-Based Inhibition of Zinc Proteases

By  

Current Medicinal Chemistry, Vol. 8, Iss. 8, 2001-07 ,pp. : 959-965

Bentham Science Publishers

Access to resources Recommend Favorite

Synthesis of benzylideneacetophenones and their inhibition of lipid peroxidation

By Arty I.S.   Timmerman H.   Samhoedi M.   Sastrohamidjojo   Sugiyanto   van der Goot H.  

European Journal of Medicinal Chemistry, Vol. 35, Iss. 4, 2000-04 ,pp. : 449-457

Elsevier

Access to resources Recommend Favorite

Selective Inhibitors of Zinc-Dependent Histone Deacetylases. Therapeutic Targets Relevant to Cancer

By  

Current Pharmaceutical Design, Vol. 21, Iss. 11, 2015-02 ,pp. : 1472-1502

Bentham Science Publishers

Access to resources Recommend Favorite