Literature DB >> 18727104

Polyvalency: a promising strategy for drug design.

David Vance1, Mrinal Shah, Amit Joshi, Ravi S Kane.   

Abstract

The simultaneous binding of multiple ligands on one entity to multiple receptors on another can result in an affinity that is significantly greater than that for the binding of a single ligand to a single receptor. This concept of "polyvalency" can be used to design molecules that are potent inhibitors of toxins and pathogens. We describe the design of potent polyvalent inhibitors that neutralize anthrax toxin in vivo as well as our attempts to elucidate the relationship between inhibitor structure and activity. We also highlight promising future avenues for research in polyvalent drug design. (c) 2008 Wiley Periodicals, Inc.

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Year:  2008        PMID: 18727104     DOI: 10.1002/bit.22056

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  19 in total

Review 1.  Inhibiting bacterial toxins by channel blockage.

Authors:  Sergey M Bezrukov; Ekaterina M Nestorovich
Journal:  Pathog Dis       Date:  2015-12-09       Impact factor: 3.166

Review 2.  Obstructing toxin pathways by targeted pore blockage.

Authors:  Ekaterina M Nestorovich; Sergey M Bezrukov
Journal:  Chem Rev       Date:  2012-10-11       Impact factor: 60.622

Review 3.  Designing inhibitors of anthrax toxin.

Authors:  Ekaterina M Nestorovich; Sergey M Bezrukov
Journal:  Expert Opin Drug Discov       Date:  2014-01-22       Impact factor: 6.098

4.  A cardiac tissue-specific binding agent of troponin I.

Authors:  Wael R Abd-Elgaliel; Ching-Hsuan Tung
Journal:  Mol Biosyst       Date:  2012-10

5.  Synthesis and Investigation of Mixed μ-Opioid and δ-Opioid Agonists as Possible Bivalent Ligands for Treatment of Pain.

Authors:  Ruben S Vardanyan; James P Cain; Saghar Mowlazadeh Haghighi; Vlad K Kumirov; Mary I McIntosh; Alexander J Sandweiss; Frank Porreca; Victor J Hruby
Journal:  J Heterocycl Chem       Date:  2016-06-01       Impact factor: 2.193

6.  Supramolecular nanostructures that mimic VEGF as a strategy for ischemic tissue repair.

Authors:  Matthew J Webber; Jörn Tongers; Christina J Newcomb; Katja-Theres Marquardt; Johann Bauersachs; Douglas W Losordo; Samuel I Stupp
Journal:  Proc Natl Acad Sci U S A       Date:  2011-08-01       Impact factor: 11.205

7.  Dependence of avidity on linker length for a bivalent ligand-bivalent receptor model system.

Authors:  Eric T Mack; Phillip W Snyder; Raquel Perez-Castillejos; Başar Bilgiçer; Demetri T Moustakas; Manish J Butte; George M Whitesides
Journal:  J Am Chem Soc       Date:  2011-12-21       Impact factor: 15.419

8.  A unique mid-sequence linker used to multimerize the lipid-phosphatidylserine (PS) binding peptide-peptoid hybrid PPS1.

Authors:  Satya Prakash Shukla; Joseph C Manarang; D Gomika Udugamasooriya
Journal:  Eur J Med Chem       Date:  2017-05-19       Impact factor: 6.514

9.  Ligand Density and Nanoparticle Clustering Cooperate in the Multivalent Amplification of Epidermal Growth Factor Receptor Activation.

Authors:  Qianyun Zhang; Björn M Reinhard
Journal:  ACS Nano       Date:  2018-10-11       Impact factor: 15.881

10.  Design, Synthesis and Biological Evaluation of β-Carboline Dimers Based on the Structure of Neokauluamine.

Authors:  Jaruwan Chatwichien; Subhasree Basu; Maureen E Murphy; Mark T Hamann; Jeffrey D Winkler
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

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