Literature DB >> 11266160

Synthesis and SAR of benzamidine factor Xa inhibitors containing a vicinally-substituted heterocyclic core.

J M Fevig1, D J Pinto, Q Han, M L Quan, J R Pruitt, I C Jacobson, R A Galemmo, S Wang, M J Orwat, L L Bostrom, R M Knabb, P C Wong, R R Wexler.   

Abstract

The selective inhibition of coagulation factor Xa has emerged as an attractive strategy for the discovery of novel antithrombotic agents. Here we describe highly potent benzamidine factor Xa inhibitors based on a vicinally-substituted heterocyclic core.

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Year:  2001        PMID: 11266160     DOI: 10.1016/s0960-894x(01)00029-4

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


  3 in total

1.  Cu(I)-catalyzed C-H alpha-amination of aryl ketones: direct synthesis of imidazolinones.

Authors:  Baoguo Zhao; Haifeng Du; Yian Shi
Journal:  J Org Chem       Date:  2009-06-05       Impact factor: 4.354

2.  Cu(I)-catalyzed sequential diamination and dehydrogenation of terminal olefins: a facile approach to imidazolinones.

Authors:  Yingguang Zhu; Yian Shi
Journal:  Chemistry       Date:  2014-09-11       Impact factor: 5.236

3.  Design, synthesis and biological evaluation of 1-Aryl-5-(4-arylpiperazine-1-carbonyl)-1H-tetrazols as novel microtubule destabilizers.

Authors:  Chao Wang; Yuelin Li; Zi Liu; Zeyu Wang; Zihan Liu; Shuai Man; Yujing Zhang; Kai Bao; Yingliang Wu; Qi Guan; Daiying Zuo; Weige Zhang
Journal:  J Enzyme Inhib Med Chem       Date:  2021-12       Impact factor: 5.051

  3 in total

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