相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Proteasome Inhibitors: An Expanding Army Attacking a Unique Target
Alexei F. Kisselev et al.
CHEMISTRY & BIOLOGY (2012)
Marizomib, a Proteasome Inhibitor for All Seasons: Preclinical Profile and a Framework for Clinical Trials
B. C. Potts et al.
CURRENT CANCER DRUG TARGETS (2011)
Cytotoxic Veraguamides, Alkynyl Bromide-Containing Cyclic Depsipeptides from the Marine Cyanobacterium cf. Oscillatoria margaritifera
Emily Mevers et al.
JOURNAL OF NATURAL PRODUCTS (2011)
Structural Basis of the Antiproliferative Activity of Largazole, a Depsipeptide Inhibitor of the Histone Deacetylases
Kathryn E. Cole et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)
Salinosporamide Natural Products: Potent 20 S Proteasome Inhibitors as Promising Cancer Chemotherapeutics
Tobias A. M. Gulder et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2010)
Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S β5-subunit
Christopher Blackburn et al.
BIOCHEMICAL JOURNAL (2010)
Evolved Diversification of a Modular Natural Product Pathway: Apratoxins F and G, Two Cytotoxic Cyclic Depsipeptides from a Palmyra Collection of Lyngbya bouillonii
Kevin Tidgewell et al.
CHEMBIOCHEM (2010)
Filamentous tropical marine cyanobacteria: a rich source of natural products for anticancer drug discovery
Lik Tong Tan
JOURNAL OF APPLIED PHYCOLOGY (2010)
Anticolon Cancer Activity of Largazole, a Marine-Derived Tunable Histone Deacetylase Inhibitor
Yanxia Liu et al.
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2010)
Two cytotoxic stereoisomers of malyngamide C, 8-epi-malyngamide C and 8-O-acetyl-8-epi-malyngamide C, from the marine cyanobacterium Lyngbya majuscula
Harald Gross et al.
PHYTOCHEMISTRY (2010)
Function-Oriented Biosynthesis of β-Lactone Proteasome Inhibitors in Salinispora tropica
Markus Nett et al.
JOURNAL OF MEDICINAL CHEMISTRY (2009)
Design and Synthesis of an Orally Bioavailable and Selective Peptide Epoxyketone Proteasome Inhibitor (PR-047)
Han-Jie Zhou et al.
JOURNAL OF MEDICINAL CHEMISTRY (2009)
NMR Quantitation of Natural Products at the Nanomole Scale
Doralyn S. Dalisay et al.
JOURNAL OF NATURAL PRODUCTS (2009)
O-GlcNAc Peptide Epoxyketones Are Recognized by Mammalian Proteasomes
Martin D. Witte et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2009)
Apratoxin A Reversibly Inhibits the Secretory Pathway by Preventing Cotranslational Translocation
Yanxia Liu et al.
MOLECULAR PHARMACOLOGY (2009)
Marine pharmacology in 2005-2006: Antitumour and cytotoxic compounds
Alejandro M. S. Mayer et al.
EUROPEAN JOURNAL OF CANCER (2008)
The potential of proteasome inhibitors in cancer therapy
Jan Sterz et al.
EXPERT OPINION ON INVESTIGATIONAL DRUGS (2008)
Structure and activity of largazole, a potent antiproliferative agent from the Floridian marine cyanobacterium Symploca sp.
Kanchan Taori et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2008)
Antitumor activity of PR-171, a novel irreversible inhibitor of the proteasome
Susan D. Demo et al.
CANCER RESEARCH (2007)
Crystal structures of salinosporamide A (NPI-0052) and B (NPI-0047) in complex with the 20S proteasome reveal important consequences of β-lactone ring opening and a mechanism for irreversible binding
M Groll et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2006)
A functional genomics approach to the mode of action of apratoxin A
H Luesch et al.
NATURE CHEMICAL BIOLOGY (2006)
Exploring protein native states and large-scale conformational changes with a modified generalized born model
A Onufriev et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2004)
Salinosporamide A: A highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus Salinospora
RH Feling et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2003)
Symplostatin 3, a new dolastatin 10 analogue from the marine cyanobacterium Symploca sp VP452
H Luesch et al.
JOURNAL OF NATURAL PRODUCTS (2002)
Crystal structure of the 20 S proteasome: TMC-95A complex: A non-covalent proteasome inhibitor
M Groll et al.
JOURNAL OF MOLECULAR BIOLOGY (2001)
Crystal structure of epoxomicin:20S proteasome reveals a molecular basis for selectivity of α′,β′-epoxyketone proteasome inhibitors
M Groll et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2000)
分享论文
