Literature DB >> 23122525

Fluorescent nitrile-based inhibitors of cysteine cathepsins.

Maxim Frizler1, Matthias D Mertens, Michael Gütschow.   

Abstract

Cysteine cathepsins play an important role in many (patho)physiological conditions. Among them, cathepsins L, S, K and B are subjects of several drug discovery programs. Besides their role as drug targets, cysteine cathepsins are additionally considered to be possible biomarkers for inflammation and cancer. Herein, we describe the design, synthesis, biological evaluation and spectral properties of fluorescently labeled dipeptide- and azadipeptide nitriles.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 23122525     DOI: 10.1016/j.bmcl.2012.09.086

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


  3 in total

Review 1.  Cysteine cathepsins: their role in tumor progression and recent trends in the development of imaging probes.

Authors:  Reik Löser; Jens Pietzsch
Journal:  Front Chem       Date:  2015-06-23       Impact factor: 5.221

2.  3-Cyano-3-aza-β-amino Acid Derivatives as Inhibitors of Human Cysteine Cathepsins.

Authors:  Janina Schmitz; Anna-Madeleine Beckmann; Adela Dudic; Tianwei Li; Robert Sellier; Ulrike Bartz; Michael Gütschow
Journal:  ACS Med Chem Lett       Date:  2014-08-11       Impact factor: 4.345

Review 3.  Molecular probes for selective detection of cysteine cathepsins.

Authors:  Kelton A Schleyer; Lina Cui
Journal:  Org Biomol Chem       Date:  2021-07-21       Impact factor: 3.890

  3 in total

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