Fullerene derivatives as a new class of inhibitors of protein tyrosine phosphatases

被引:22
作者
Kobzar, Oleksandr L. [1 ]
Trush, Viacheslav V. [1 ]
Tanchuk, Vsevolod Yu [1 ]
Zhilenkov, Alexander V. [2 ]
Troshin, Pavel A. [2 ]
Vovk, Andriy I. [1 ]
机构
[1] Natl Acad Sci Ukraine, Inst Bioorgan Chem & Petrochem, UA-02660 Kiev 94, Ukraine
[2] Russian Acad Sci, Inst Problems Chem Phys, Chernogolovka 142432, Moscow Region, Russia
基金
俄罗斯基础研究基金会;
关键词
Protein tyrosine phosphatase; Fullerene; Inhibition; Molecular docking; METHYLENEBISPHOSPHONIC ACIDS; POLYMERASE INHIBITION; SELECTIVE INHIBITORS; STRUCTURAL BASIS; POTENT; PTP1B; DESIGN; ALPHA; CD45; TOXICITY;
D O I
10.1016/j.bmcl.2014.04.110
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study, we identified water-soluble C-60 and C-70 fullerene derivatives as a novel class of protein tyrosine phosphatase inhibitors. The evaluated compounds were found to inhibit CD45, PTP1B, TC-PTP, SHP2, and PTPB with IC50 values in the low micromolar to high nanomolar range. These results demonstrate a new strategy for designing effective nanoscale protein tyrosine phosphatase inhibitors. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3175 / 3179
页数:5
相关论文
共 74 条
[1]   Tyrosine phosphatase SHP2 promotes breast cancer progression and maintains tumor-initiating cells via activation of key transcription factors and a positive feedback signaling loop [J].
Aceto, Nicola ;
Sausgruber, Nina ;
Brinkhaus, Heike ;
Gaidatzis, Dimos ;
Martiny-Baron, Georg ;
Mazzarol, Giovanni ;
Confalonieri, Stefano ;
Quarto, Micaela ;
Hu, Guang ;
Balwierz, Piotr J. ;
Pachkov, Mikhail ;
Elledge, Stephen J. ;
van Nimwegen, Erik ;
Stadler, Michael B. ;
Bentires-Alj, Mohamed .
NATURE MEDICINE, 2012, 18 (04) :529-537
[2]   Protein tyrosine phosphatases in the human genome [J].
Alonso, A ;
Sasin, J ;
Bottini, N ;
Friedberg, I ;
Friedberg, I ;
Osterman, A ;
Godzik, A ;
Hunter, T ;
Dixon, J ;
Mustelin, T .
CELL, 2004, 117 (06) :699-711
[3]   Review of fullerene toxicity and exposure - Appraisal of a human health risk assessment, based on open literature [J].
Aschberger, Karin ;
Johnston, Helinor J. ;
Stone, Vicki ;
Aitken, Robert J. ;
Tran, C. Lang ;
Hankin, Steven M. ;
Peters, Sheona A. K. ;
Christensen, Frans M. .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2010, 58 (03) :455-473
[4]   Large-Scale Structural Analysis of the Classical Human Protein Tyrosine Phosphatome [J].
Barr, Alastair J. ;
Ugochukwu, Emilie ;
Lee, Wen Hwa ;
King, Oliver N. F. ;
Filippakopoulos, Panagis ;
Alfano, Ivan ;
Savitsky, Pavel ;
Burgess-Brown, Nicola A. ;
Mueller, Susanne ;
Knapp, Stefan .
CELL, 2009, 136 (02) :352-363
[5]   Protein tyrosine phosphatase structure-function relationships in regulation and pathogenesis [J].
Boehmer, Frank ;
Szedlacsek, Stefan ;
Tabernero, Lydia ;
Ostman, Arne ;
den Hertog, Jeroen .
FEBS JOURNAL, 2013, 280 (02) :413-431
[6]   Fullerene derivatives: an attractive tool for biological applications [J].
Bosi, S ;
Da Ros, T ;
Spalluto, G ;
Prato, M .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2003, 38 (11-12) :913-923
[7]   Divalent and trivalent α-ketocarboxylic acids as inhibitors of protein tyrosine phosphatases [J].
Chen, YT ;
Seto, CT .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (18) :3946-3952
[8]   FREE-RADICAL SCAVENGING ACTIVITY OF WATER-SOLUBLE FULLERENOLS [J].
CHIANG, LY ;
LU, FJ ;
LIN, JT .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (12) :1283-1284
[9]   Glycosidase Inhibition with Fullerene Iminosugar Balls: A Dramatic Multivalent Effect [J].
Compain, Philippe ;
Decroocq, Camille ;
Iehl, Julien ;
Holler, Michel ;
Hazelard, Damien ;
Mena Barragan, Teresa ;
Ortiz Mellet, Carmen ;
Nierengarten, Jean-Francois .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (33) :5753-5756
[10]   Computational design of novel fullerene analogues as potential HIV-1 PR inhibitors: Analysis of the binding interactions between fullerene inhibitors and HIV-1 PR residues using 3D QSAR, molecular docking and molecular dynamics simulations [J].
Durdagi, Serdar ;
Mavromoustakos, Thomas ;
Chronakis, Nikos ;
Papadopoulos, Manthos G. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (23) :9957-9974