Literature DB >> 20449263

Enzymatic activation of a matrix metalloproteinase inhibitor.

Jody L Major Jourden1, Seth M Cohen.   

Abstract

Matrix metalloproteinase inhibitors (MMPi) possessing a glucose protecting group on the zinc-binding group (ZBG) show a dramatic increase in inhibitory activity upon cleavage by beta-glucosidase.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20449263      PMCID: PMC2867072          DOI: 10.1039/b923302d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  32 in total

1.  Design and therapeutic application of matrix metalloproteinase inhibitors.

Authors:  M Whittaker; C D Floyd; P Brown; A J Gearing
Journal:  Chem Rev       Date:  1999-09-08       Impact factor: 60.622

2.  Carbonic anhydrase inhibitors: Hypoxia-activatable sulfonamides incorporating disulfide bonds that target the tumor-associated isoform IX.

Authors:  Giuseppina De Simone; Rosa Maria Vitale; Anna Di Fiore; Carlo Pedone; Andrea Scozzafava; Jean-Louis Montero; Jean-Yves Winum; Claudiu T Supuran
Journal:  J Med Chem       Date:  2006-09-07       Impact factor: 7.446

3.  Design, synthesis, and biological activity of folate receptor-targeted prodrugs of thiolate histone deacetylase inhibitors.

Authors:  Takayoshi Suzuki; Shinya Hisakawa; Yukihiro Itoh; Nobuaki Suzuki; Katsumasa Takahashi; Masatoshi Kawahata; Kentaro Yamaguchi; Hidehiko Nakagawa; Naoki Miyata
Journal:  Bioorg Med Chem Lett       Date:  2007-05-17       Impact factor: 2.823

Review 4.  MMPs as therapeutic targets--still a viable option?

Authors:  Barbara Fingleton
Journal:  Semin Cell Dev Biol       Date:  2007-07-06       Impact factor: 7.727

5.  Tissue inhibitor of metalloproteinases 3 regulates extracellular matrix--cell signaling during bronchiole branching morphogenesis.

Authors:  Sean E Gill; M Cynthia Pape; Kevin J Leco
Journal:  Dev Biol       Date:  2006-07-12       Impact factor: 3.582

6.  Synthesis and biological evaluation of the suberoylanilide hydroxamic acid (SAHA) beta-glucuronide and beta-galactoside for application in selective prodrug chemotherapy.

Authors:  Mickaël Thomas; Freddy Rivault; Isabelle Tranoy-Opalinski; Joëlle Roche; Jean-Pierre Gesson; Sébastien Papot
Journal:  Bioorg Med Chem Lett       Date:  2006-11-17       Impact factor: 2.823

Review 7.  Strategies for MMP inhibition in cancer: innovations for the post-trial era.

Authors:  Christopher Mark Overall; Carlos López-Otín
Journal:  Nat Rev Cancer       Date:  2002-09       Impact factor: 60.716

8.  A novel coumarin-labelled peptide for sensitive continuous assays of the matrix metalloproteinases.

Authors:  C G Knight; F Willenbrock; G Murphy
Journal:  FEBS Lett       Date:  1992-01-27       Impact factor: 4.124

9.  New beginnings for matrix metalloproteinase inhibitors: identification of high-affinity zinc-binding groups.

Authors:  David T Puerta; Jana A Lewis; Seth M Cohen
Journal:  J Am Chem Soc       Date:  2004-07-14       Impact factor: 15.419

10.  Synthesis, characterization, and metal coordinating ability of multifunctional carbohydrate-containing compounds for Alzheimer's therapy.

Authors:  Tim Storr; Michael Merkel; George X Song-Zhao; Lauren E Scott; David E Green; Meryn L Bowen; Katherine H Thompson; Brian O Patrick; Harvey J Schugar; Chris Orvig
Journal:  J Am Chem Soc       Date:  2007-05-19       Impact factor: 15.419

View more
  5 in total

1.  Investigation of self-immolative linkers in the design of hydrogen peroxide activated metalloprotein inhibitors.

Authors:  Jody L Major Jourden; Kevin B Daniel; Seth M Cohen
Journal:  Chem Commun (Camb)       Date:  2011-06-16       Impact factor: 6.222

Review 2.  Emerging trends in metalloprotein inhibition.

Authors:  Matthieu Rouffet; Seth M Cohen
Journal:  Dalton Trans       Date:  2011-02-02       Impact factor: 4.390

3.  Hydrogen peroxide activated matrix metalloproteinase inhibitors: a prodrug approach.

Authors:  Jody L Major Jourden; Seth M Cohen
Journal:  Angew Chem Int Ed Engl       Date:  2010-09-10       Impact factor: 15.336

4.  Evaluating prodrug strategies for esterase-triggered release of alcohols.

Authors:  Christian Perez; Kevin B Daniel; Seth M Cohen
Journal:  ChemMedChem       Date:  2013-08-08       Impact factor: 3.466

5.  The feasibility of enzyme targeted activation for amino acid/dipeptide monoester prodrugs of floxuridine; cathepsin D as a potential targeted enzyme.

Authors:  Yasuhiro Tsume; Gordon L Amidon
Journal:  Molecules       Date:  2012-03-26       Impact factor: 4.411

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.