Supplemental material
Open access
1,799
Views
10
CrossRef citations to date
0
Altmetric
Original Article
Naphthoquinone amino acid derivatives, synthesis and biological activity as proteasome inhibitors
Mauro MarastoniDepartment of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy;
, Claudio TrapellaDepartment of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy;
, Alessandra ScottiDepartment of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy;
, Anna FantinatiDepartment of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy;
, Valeria FerrettiDepartment of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy;
, Erika MarzolaDepartment of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy;
, Gallerani EleonoraDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy
, Riccardo GavioliDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy
& Delia PretiDepartment of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy; Correspondence[email protected]
http://orcid.org/0000-0002-1075-3781
Pages 865-877
|
Received 03 Apr 2017, Accepted 15 May 2017, Published online: 28 Jun 2017
Related Research Data
Proteasome Inhibitors: An Expanding Army Attacking a Unique Target
Source:
Elsevier BV
Arecoline tripeptide inhibitors of proteasome.
Source:
American Chemical Society (ACS)
Phase 1 study of twice-weekly ixazomib, an oral proteasome inhibitor, in relapsed/refractory multiple myeloma patients.
Source:
American Society of Hematology
Global analysis of proteasomal substrate specificity using positional-scanning libraries of covalent inhibitors
Source:
Proceedings of the National Academy of Sciences
Re-examination and further development of a precise and rapid dye method for measuring cell growth/cell kill
Source:
Elsevier BV
Antitumor Activity of PR-171, a Novel Irreversible Inhibitor of the Proteasome
Source:
American Association for Cancer Research (AACR)
α,β-Unsaturated N-Acylpyrrole Peptidyl Derivatives: New Proteasome Inhibitors
Source:
American Chemical Society (ACS)
The development of proteasome inhibitors as anticancer drugs
Source:
Elsevier BV
Design and Synthesis of an Orally Bioavailable and Selective Peptide Epoxyketone Proteasome Inhibitor (PR-047)
Source:
American Chemical Society (ACS)
Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94
Source:
Wiley
Proteolysis: from the lysosome to ubiquitin and the proteasome.
Source:
Springer Science and Business Media LLC
Proteasome Inhibition
Source:
Wiley
Crystal Structure of Epoxomicin:20S Proteasome Reveals a Molecular Basis for Selectivity of α‘,β‘-Epoxyketone Proteasome Inhibitors
Source:
American Chemical Society (ACS)
α,β-Unsaturated Carbonyl System of Chalcone-Based Derivatives is Responsible for Broad Inhibition of Proteasomal Activity and Preferential Killing of Human Papilloma Virus (HPV)-Positive Cervical Cancer Cells
Source:
American Chemical Society (ACS)
Studies of the synthesis of all stereoisomers of MG-132 proteasome inhibitors in the tumor targeting approach.
Source:
American Chemical Society (ACS)
Discovery and Synthesis of Hydronaphthoquinones as Novel Proteasome Inhibitors
Source:
American Chemical Society (ACS)
Dimerized linear mimics of a natural cyclopeptide (TMC-95A) are potent noncovalent inhibitors of the eukaryotic 20S proteasome.
Source:
HAL CCSD
PEPTIDE-BASED PROTEASOME INHIBITORS
Source:
Wiley
Synthesis and biological evaluation of naphthoquinone analogs as a novel class of proteasome inhibitors.
Source:
Elsevier BV
Recognition and Processing of Ubiquitin-Protein Conjugates by the Proteasome
Source:
Annual Reviews
Related research
People also read lists articles that other readers of this article have read.
Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.
Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.