Design, Synthesis and Biological Evaluation of Ferulic Acid Amides as Selective Matrix Metalloproteinase Inhibitors

Publisher： Bentham Science Publishers

E-ISSN： 1875-6638|9|7|947-954

ISSN： 1573-4064

Source： Medicinal Chemistry, Vol.9, Iss.7, 2013-11, pp. : 947-954

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

Design, synthesis, and biological evaluation of 2-substituted ethenesulfonic acid ester derivatives as selective PTP1B inhibitors

By Liu Jingbao   Deng Xinxian   Jin Yan   Xu Buzhe   Liu Wenlu   Jiang Faqin   Fu Lei  

Die Pharmazie - An International Journal of Pharmaceutical Sciences, Vol. 70, Iss. 7, 2015-07 ,pp. : 446-451

Govi-Verlag

Access to resources Recommend Favorite

Selective Matrix Metalloproteinase Inhibitors for Cancer

By  

Current Medicinal Chemistry, Vol. 16, Iss. 29, 2009-10 ,pp. : 3805-3827

Bentham Science Publishers

Access to resources Recommend Favorite

Design, Synthesis, and Biological Evaluation of Vanillin Hydroxamic Acid Derivatives as Novel Peptide Deformylase Inhibitors

By  

Current Computer - Aided Drug Design, Vol. 14, Iss. 1, 2018-03 ,pp. : 95-101

Bentham Science Publishers

Access to resources Recommend Favorite

Design, Synthesis and Biological Evaluation of Novel Non-peptide Boronic Acid Derivatives as Proteasome Inhibitors

By  

Medicinal Chemistry, Vol. 10, Iss. 1, 2014-02 ,pp. : 38-45

Bentham Science Publishers

Access to resources Recommend Favorite

The Design, Structure, and Therapeutic Application of Matrix Metalloproteinase Inhibitors

By  

Current Medicinal Chemistry, Vol. 8, Iss. 4, 2001-03 ,pp. : 425-474

Bentham Science Publishers

Access to resources Recommend Favorite