Iminosugars past, present and future: medicines for tomorrow.
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D. H. Williams | F. Wilson | R. Storer | Graeme Horne | Francis X Wilson | Jon Tinsley | David H Williams | Richard Storer | G. Horne | Jon Tinsley
[1] D. Burton,et al. N-Butyldeoxynojirimycin is a broadly effective anti-HIV therapy significantly enhanced by targeted liposome delivery , 2008, AIDS.
[2] A. Watson,et al. Iminosugars from Baphia nitida Lodd. , 2008, Phytochemistry.
[3] A. Ballabio,et al. Pharmacological Enhancement of Mutated α-Glucosidase Activity in Fibroblasts from Patients with Pompe Disease. , 2007, Molecular therapy : the journal of the American Society of Gene Therapy.
[4] P. Sharma,et al. Scale-Up Synthesis of Swainsonine: A Potent α-Mannosidase II Inhibitor† , 2008 .
[5] P. Compain,et al. Tactics and strategies for the synthesis of iminosugar C-glycosides: a review , 2009 .
[6] S. Inouye,et al. The structure of nojirimycin, a piperidinose sugar antibiotic. , 1966, The Journal of antibiotics.
[7] Chung-Yi Wu,et al. Glycan array: a powerful tool for glycomics studies , 2009, Expert review of proteomics.
[8] Raymond A. Dwek,et al. Glycobiology: Toward Understanding the Function of Sugars. , 1996, Chemical reviews.
[9] H. Overkleeft,et al. Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation. , 2010, Journal of medicinal chemistry.
[10] L. Cipolla,et al. Combinatorial approaches to iminosugars as glycosidase and glycosyltransferase inhibitors. , 2006, Combinatorial chemistry & high throughput screening.
[11] Naoyuki Taniguchi,et al. Aberrant expression of N-acetylglucosaminyltransferase-IVa and IVb (GnT-IVa and b) in pancreatic cancer. , 2006, Biochemical and biophysical research communications.
[12] M. Lotz,et al. Hexosaminidase inhibitors as new drug candidates for the therapy of osteoarthritis. , 2001, Chemistry & biology.
[13] Koichiro Yoshino,et al. CB-12181, a new azasugar-based matrix metalloproteinase/tumor necrosis factor-alpha converting enzyme inhibitor, inhibits vascular endothelial growth factor-induced angiogenesis in vitro and retinal neovascularization in vivo. , 2009, Current Neurovascular Research.
[14] Li-he Zhang,et al. Rapid Synthesis of Iminosugar Derivatives for Cell‐Based In Situ Screening: Discovery of “Hit” Compounds with Anticancer Activity , 2007, ChemMedChem.
[15] O. Reiser,et al. Stereoselective Synthesis of Swainsonines from Pyridines , 2005 .
[16] L. Presta,et al. Inhibitory Fc receptors modulate in vivo cytoxicity against tumor targets , 2000, Nature Medicine.
[17] R. Clarkson,et al. Large scale synthesis of the acetonides of l-glucuronolactone and of l-glucose: easy access to l-sugar chirons , 2009 .
[18] Mattie S. M. Timmer,et al. Recent Developments in the Synthesis of Pyrrolidine‐Containing Iminosugars , 2010 .
[19] P. D. Lilley,et al. Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases. , 1998, Journal of medicinal chemistry.
[20] R. Lachmann. Miglustat: substrate reduction therapy for glycosphingolipid lysosomal storage disorders. , 2006, Drugs of today.
[21] Tibor Kozár,et al. Glycan and lectin microarrays for glycomics and medicinal applications , 2010, Medicinal research reviews.
[22] Annalisa Guaragna,et al. Glycomimetics at the mirror: medicinal chemistry of L-iminosugars. , 2009, Current medicinal chemistry.
[23] Jian‐Qiang Fan. Iminosugars as Active‐Site‐Specific Chaperones for the Treatment of Lysosomal Storage Disorders , 2008 .
[24] J. Dubuisson,et al. Involvement of Endoplasmic Reticulum Chaperones in the Folding of Hepatitis C Virus Glycoproteins , 1998, Journal of Virology.
[25] F. Nicotra,et al. General Strategies for the Synthesis of Iminosugars and New Approaches Towards Iminosugar Libraries , 2007 .
[26] R. Spiro. Protein glycosylation: nature, distribution, enzymatic formation, and disease implications of glycopeptide bonds. , 2002, Glycobiology.
[27] K. Mansfield,et al. Natural iminosugar derivatives of 1-deoxynojirimycin inhibit glycosylation of hepatitis viral envelope proteins. , 2007, Journal of microbiology.
[28] J. E. Thomson,et al. Iodine-mediated ring-closing iodoamination with concomitant N-debenzylation for the asymmetric synthesis of polyhydroxylated pyrrolidines , 2009 .
[29] P. Smith,et al. Synthesis of deoxymannojirimycin fagomine deoxynojirimycin 2-acetamido-1,5-imino-1,2,5-trideoxy-D-mannitol 2-acetamido-1,5-imino-1,2,5-trideoxy-D-glucitol 2S,3R,4R,5R-trihydroxypipecolic acid and 2S,3R,4R,5S-trihydroxypipecolic acid from methyl 3-O-benzyl-2,6-dideoxy-2,6-imino-α-D-mannofuranoside , 1987 .
[30] F. Platt,et al. Medicinal use of iminosugars , 2008 .
[31] A. Elbein,et al. Swainsonine: an inhibitor of glycoprotein processing. , 1981, Proceedings of the National Academy of Sciences of the United States of America.
[32] S. Nishimura,et al. Azasugar-based MMP/ADAM inhibitors as antipsoriatic agents. , 2004, Journal of medicinal chemistry.
[33] N. Asano. Naturally occurring iminosugars and related compounds: structure, distribution, and biological activity. , 2003, Current topics in medicinal chemistry.
[34] R. Moriarty,et al. Novel Imino Sugar Derivatives Demonstrate Potent Antiviral Activity against Flaviviruses , 2009, Antimicrobial Agents and Chemotherapy.
[35] Lihua Yu,et al. Suppression of FUT1/FUT4 expression by siRNA inhibits tumor growth. , 2008, Biochimica et biophysica acta.
[36] V. Ranade. Iminosugars-From Synthesis to Therapeutic Applications , 2009 .
[37] M. Wormald,et al. Cystic fibrosis and diabetes: isoLAB and isoDAB, enantiomeric carbon-branched pyrrolidine iminosugars , 2010 .
[38] Benjamin G Davis,et al. Glyco- and peptidomimetics from three-component Joullié-Ugi coupling show selective antiviral activity. , 2005, Journal of the American Chemical Society.
[39] T. Aoyagi,et al. Purification and characterization of a sialidase inhibitor, siastatin, produced by Streptomyces. , 1974, The Journal of antibiotics.
[40] I. Izquierdo,et al. Polyhydroxylated pyrrolizidines. Part 6 : A new and concise stereoselective synthesis of ( + )-casuarine and its 6,7-diepi isomer, from DMDP , 2005 .
[41] T. Butters,et al. Rational design and synthesis of highly potent pharmacological chaperones for treatment of N370S mutant Gaucher disease. , 2009, Journal of medicinal chemistry.
[42] R. Dwek,et al. Secretion of human hepatitis B virus is inhibited by the imino sugar N-butyldeoxynojirimycin. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[43] L. Sorbera,et al. Celgosivir: α-Glucosidase inhibitor anti-hepatitis C virus drug , 2005 .
[44] J. Marth,et al. Glycosylation in Cellular Mechanisms of Health and Disease , 2006, Cell.
[45] Shui-Tein Chen,et al. Synthesis of DMJ analogs with seven- and eight-membered iminocyclitols , 2007 .
[46] R. Dwek,et al. Inhibition of hepatitis B virus DNA replication by imino sugars without the inhibition of the DNA polymerase: Therapeutic implications , 2001, Hepatology.
[47] R. Dwek,et al. Looking glass inhibitors: efficient synthesis and biological evaluation of D-deoxyfuconojirimycin. , 2005, Carbohydrate research.
[48] A. Varki,et al. Biological roles of oligosaccharides: all of the theories are correct , 1993, Glycobiology.
[49] Richard D. Cummings,et al. The repertoire of glycan determinants in the human glycome. , 2009, Molecular bioSystems.
[50] T. Donohoe,et al. Synthesis of (+)-DGDP and (-)-7-epialexine. , 2008, Organic & biomolecular chemistry.
[51] S. Kornfeld,et al. Assembly of asparagine-linked oligosaccharides. , 1985, Annual review of biochemistry.
[52] D. Loo,et al. Imino Sugars Are Potent Agonists of the Human Glucose Sensor SGLT3 , 2007, Molecular Pharmacology.
[53] Pere Clapés,et al. D-fructose-6-phosphate aldolase in organic synthesis: cascade chemical-enzymatic preparation of sugar-related polyhydroxylated compounds. , 2009, Chemistry.
[54] M. Bols,et al. THE FIRST COMBINATORIAL LIBRARY OF AZASUGAR GLYCOSIDASE INHIBITORS , 1999 .
[55] B. Winchester. Iminosugars: from botanical curiosities to licensed drugs , 2009 .
[56] K. Matsumoto,et al. Inhibition of experimental metastasis by castanospermine in mice: blockage of two distinct stages of tumor colonization by oligosaccharide processing inhibitors. , 1986, Cancer research.
[57] P. Compain,et al. Design, synthesis and biological evaluation of iminosugar-based glycosyltransferase inhibitors. , 2003, Current topics in medicinal chemistry.
[58] Kami Kim,et al. Transition State Analogue Inhibitors of Purine Nucleoside Phosphorylase from Plasmodium falciparum * , 2002, The Journal of Biological Chemistry.
[59] M. Wormald,et al. Polyhydroxylated pyrrolidine and pyrrolizidine alkaloids from Hyancinthoides non-scripta and Scilla campanulata. , 1999, Carbohydrate research.
[60] L. Agius,et al. Diverse effects of two allosteric inhibitors on the phosphorylation state of glycogen phosphorylase in hepatocytes. , 2002, The Biochemical journal.
[61] Toshihide Kobayashi,et al. Molecular interaction of imino sugars with human alpha-galactosidase: Insight into the mechanism of complex formation and pharmacological chaperone action in Fabry disease. , 2009, Molecular genetics and metabolism.
[62] T. Harris,et al. Identification of swainsonine as a probable contributory mycotoxin in moldy forage mycotoxicoses , 1984, Applied and environmental microbiology.
[63] L. Kiessling,et al. Chemical approaches to glycobiology. , 2010, Annual review of biochemistry.
[64] R. Hopkin,et al. Fabry's disease , 2008, The Lancet.
[65] A. Reuser,et al. Pompe's disease , 2008, The Lancet.
[66] Chen Wang,et al. Looking glass inhibitors: scalable syntheses of DNJ, DMDP, and (3R)-3-hydroxy-l-bulgecinine from d-glucuronolactone and of l-DNJ, l-DMDP, and (3S)-3-hydroxy-d-bulgecinine from l-glucuronolactone. DMDP inhibits β-glucosidases and β-galactosidases whereas l-DMDP is a potent and specific inhibitor of α , 2010 .
[67] H. Ploegh,et al. Interference with HIV-induced syncytium formation and viral infectivity by inhibitors of trimming glucosidase , 1987, Nature.
[68] Carolyn R. Bertozzi,et al. Essentials of Glycobiology , 1999 .
[69] H. Kajiyama,et al. High expression of N-acetylglucosaminyltransferase V in mucinous tumors of the ovary. , 2009, Oncology reports.
[70] W. Cornell,et al. Discovery of potent, selective, and orally active carboxylic acid based inhibitors of matrix metalloproteinase-13. , 2009, Journal of medicinal chemistry.
[71] R. Dwek,et al. Cellular effects of deoxynojirimycin analogues: uptake, retention and inhibition of glycosphingolipid biosynthesis. , 2004, The Biochemical journal.
[72] G. Besra,et al. Synthesis of the naringinase inhibitors l-swainsonine and related 6-C-methyl-l-swainsonine analogues: (6R)-C-methyl-l-swainsonine is a more potent inhibitor of l-rhamnosidase by an order of magnitude than l-swainsonine , 2008 .
[73] J. Hoffman,et al. Mutation analysis of B3GALTL in Peters Plus syndrome , 2008, American journal of medical genetics. Part A.
[74] O. Morand,et al. The pharmacokinetics and tissue distribution of the glucosylceramide synthase inhibitor miglustat in the rat , 2007, Xenobiotica; the fate of foreign compounds in biological systems.
[75] J. E. Wraith,et al. New therapies in the management of Niemann-Pick type C disease: clinical utility of miglustat , 2009 .
[76] René Ranzinger,et al. Exploring the structural diversity of mammalian carbohydrates ("glycospace") by statistical databank analysis. , 2007, ACS chemical biology.
[77] Hudson H. Freeze,et al. Genetic defects in the human glycome , 2006, Nature Reviews Genetics.
[78] K. Yasuda,et al. Polyhydroxylated alkaloids isolated from mulberry trees (Morusalba L.) and silkworms (Bombyx mori L.). , 2001, Journal of agricultural and food chemistry.
[79] J. M. Aerts,et al. Inhibition of Glycosphingolipid Synthesis Induces a Profound Reduction of Plasma Cholesterol and Inhibits Atherosclerosis Development in APOE*3 Leiden and Low-Density Lipoprotein Receptor−/− Mice , 2010, Arteriosclerosis, thrombosis, and vascular biology.
[80] Haibing Guo,et al. DE NOVO ASYMMETRIC APPROACH TO 8a-epi-SWAINSONINE , 2009 .
[81] D. Rowlands,et al. Genotype‐dependent sensitivity of hepatitis C virus to inhibitors of the p7 ion channel , 2008, Hepatology.
[82] A. Watson,et al. Polyhydroxylated alkaloids -- natural occurrence and therapeutic applications. , 2001, Phytochemistry.
[83] A. Sacchetti,et al. A chemoenzymatic-RCM strategy for the enantioselective synthesis of new dihydroxylated 5-hydroxymethyl-indolizidines and 6-hydroxymethyl-quinolizidines , 2007 .
[84] R. Janzer,et al. Functionalized pyrrolidine inhibitors of human type II alpha-mannosidases as anti-cancer agents: optimizing the fit to the active site. , 2008, Bioorganic & medicinal chemistry.
[85] C. Mandal,et al. Elevated mRNA level of hST6Gal I and hST3Gal V positively correlates with the high risk of pediatric acute leukemia. , 2010, Leukemia research.
[86] T. Andresen,et al. A concise synthesis of castanospermine by the use of a transannular cyclization. , 2009, The Journal of organic chemistry.
[87] N. Callewaert,et al. Glycome profiling using modern glycomics technology: technical aspects and applications , 2010, Biological chemistry.
[88] S. Denmark,et al. Synthesis of (+)-casuarine. , 2000, The Journal of organic chemistry.
[89] Paul W Smith,et al. Inhibition of HIV replication by amino‐sugar derivatives , 1988, FEBS letters.
[90] P. Lebecque,et al. Airway delivery of low-dose miglustat normalizes nasal potential difference in F508del cystic fibrosis mice. , 2009, American journal of respiratory and critical care medicine.
[91] G. Fleet,et al. Looking glass inhibitors: synthesis of a potent naringinase inhibitor l-DIM [1,4-dideoxy-1,4-imino-l-mannitol], the enantiomer of DIM [1,4-dideoxy-1,4-imino-d-mannitol] a potent α-d-mannosidase inhibitor , 2007 .