Sulfur Derivatives of the Natural Polyarsenical Arsenicin A: Biologically Active, Organometallic Arsenic–Sulfur Cages Related to the Minerals Realgar and Uzonite
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G. Salem | P. Hogg | M. Coote | A. Willis | S. Arulmozhiraja | P. Dilda | A. Rae | S. Benhenda | Di-Qiu Lu | S. Wild | Xiaoyi Zhai | V. Breitenbach
[1] Yuan Liu,et al. Critical role of cellular glutathione homeostasis for trivalent inorganic arsenite-induced oxidative damage in human bronchial epithelial cells. , 2014, Mutation research. Genetic toxicology and environmental mutagenesis.
[2] N. Setterblad,et al. Oxidative stress–induced assembly of PML nuclear bodies controls sumoylation of partner proteins , 2014, The Journal of cell biology.
[3] G. Salem,et al. 1040 Polyarsenic Adamantane-type Compounds – a Promising New Class of Drugs for the Treatment of Drug-resistant Ovarian Cancers , 2012 .
[4] P. Hogg,et al. The tumour metabolism inhibitors GSAO and PENAO react with cysteines 57 and 257 of mitochondrial adenine nucleotide translocase , 2012, Cancer Cell International.
[5] C. Lin,et al. Resolution and improved synthesis of (±)-arsenicin A: A natural adamantane-type tetraarsenical possessing strong anti-acute promelocytic leukemia cell line activity , 2012 .
[6] G. Salem,et al. Origin of the unusual ultraviolet absorption of Arsenicin A. , 2011, The journal of physical chemistry. A.
[7] A. Bagno. Computing the NMR spectra of the sponge metabolite arsenicin A: when simple becomes difficult , 2010 .
[8] B. Raught,et al. PML/RARA oxidation and arsenic binding initiate the antileukemia response of As2O3. , 2010, Cancer cell.
[9] I. Koch,et al. 6:Organoarsenicals. Distribution and Transformation in the Environment , 2010 .
[10] G. Salem,et al. Arsenicin A, A Natural Polyarsenical: Synthesis and Crystal Structure , 2010 .
[11] I. Koch,et al. Organoarsenicals. Distribution and transformation in the environment. , 2010, Metal ions in life sciences.
[12] P. Hogg,et al. Optimization of the antitumor efficacy of a synthetic mitochondrial toxin by increasing the residence time in the cytosol. , 2009, Journal of medicinal chemistry.
[13] G. Mariotto,et al. Vibrational analysis as a powerful tool in structure elucidation of polyarsenicals: a DFT-based investigation of arsenicin A. , 2009, Physical chemistry chemical physics : PCCP.
[14] G. Guella,et al. Computational NMR spectroscopy of organoarsenicals and the natural polyarsenic compound arsenicin A. , 2008, Chemistry.
[15] L. Bindi,et al. A crystallographic review of arsenic sulfides: effects of chemical variations and changes induced by exposure to light , 2008 .
[16] R. Lock,et al. Insight into the selectivity of arsenic trioxide for acute promyelocytic leukemia cells by characterizing Saccharomyces cerevisiae deletion strains that are sensitive or resistant to the metalloid. , 2008, The international journal of biochemistry & cell biology.
[17] P. Hogg,et al. Arsenical-based cancer drugs. , 2007, Cancer treatment reviews.
[18] G. Guella,et al. On the first polyarsenic organic compound from nature: arsenicin A from the New Caledonian marine sponge Echinochalina bargibanti. , 2006, Chemistry.
[19] V. Higgins,et al. Mechanism of selectivity of an angiogenesis inhibitor from screening a genome-wide set of Saccharomyces cerevisiae deletion strains. , 2005, Journal of the National Cancer Institute.
[20] Andreas Dreuw,et al. Single-reference ab initio methods for the calculation of excited states of large molecules. , 2005, Chemical reviews.
[21] Richard I. Cooper,et al. CRYSTALS version 12: software for guided crystal structure analysis , 2003 .
[22] L. Bindi,et al. UZONITE, As4S5, FROM THE TYPE LOCALITY: SINGLE-CRYSTAL X-RAY STUDY AND EFFECTS OF EXPOSURE TO LIGHT , 2003 .
[23] J. Folkman,et al. A peptide trivalent arsenical inhibits tumor angiogenesis by perturbing mitochondrial function in angiogenic endothelial cells. , 2003, Cancer cell.
[24] P. Hogg,et al. Presence of closely spaced protein thiols on the surface of mammalian cells , 2000, Protein science : a publication of the Protein Society.
[25] G. Scuseria,et al. An efficient implementation of time-dependent density-functional theory for the calculation of excitation energies of large molecules , 1998 .
[26] Dennis R. Salahub,et al. Molecular excitation energies to high-lying bound states from time-dependent density-functional response theory: Characterization and correction of the time-dependent local density approximation ionization threshold , 1998 .
[27] R. Ahlrichs,et al. Treatment of electronic excitations within the adiabatic approximation of time dependent density functional theory , 1996 .
[28] C Haanen,et al. A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V. , 1995, Journal of immunological methods.
[29] A. Becke. Density-functional thermochemistry. III. The role of exact exchange , 1993 .
[30] A. Willis,et al. Enantioselective biotransformation of ethyl-n-propylarsinic acid by the mould Scopulariopsis brevicaulis: asymmetric synthesis of (R)-ethylmethyl-n-propylarsine , 1990 .
[31] Parr,et al. Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density. , 1988, Physical review. B, Condensed matter.
[32] T. Mosmann. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. , 1983, Journal of immunological methods.
[33] A. Rae. Crystal structure refinement using a number of orthonormal axial systems , 1975 .
[34] W. Nowacki,et al. Refinement of the crystal structures of realgar, AsS and orpiment, As2S3 , 1972 .