Year |
Citation |
Score |
2016 |
Avizienyte E, Cole CL, Rushton G, Miller GJ, Bugatti A, Presta M, Gardiner JM, Jayson GC. Synthetic Site-Selectively Mono-6-O-Sulfated Heparan Sulfate Dodecasaccharide Shows Anti-Angiogenic Properties In Vitro and Sensitizes Tumors to Cisplatin In Vivo. Plos One. 11: e0159739. PMID 27490176 DOI: 10.1371/Journal.Pone.0159739 |
0.456 |
|
2016 |
Potter GT, Jayson GC, Miller GJ, Gardiner JM. An updated synthesis of the diazo-transfer reagent imidaz-ole-1-sulfonyl azide hydrogen sulfate. The Journal of Organic Chemistry. PMID 26998999 DOI: 10.1021/Acs.Joc.6B00177 |
0.496 |
|
2015 |
Hansen SU, Miller GJ, Cliff MJ, Jayson GC, Gardiner JM. Making the longest sugars: a chemical synthesis of heparin-related [4] oligosaccharides from 16-mer to 40-mer. Chemical Science. 6: 6158-6164. PMID 30090231 DOI: 10.1039/C5Sc02091C |
0.516 |
|
2015 |
Miller GJ, Broberg KR, Rudd C, Helliwell MR, Jayson GC, Gardiner JM. A latent reactive handle for functionalising heparin-like and LMWH deca- and dodecasaccharides. Organic & Biomolecular Chemistry. PMID 26381107 DOI: 10.1039/C5Ob01706H |
0.499 |
|
2015 |
Jayson GC, Hansen SU, Miller GJ, Cole CL, Rushton G, Avizienyte E, Gardiner JM. Synthetic heparan sulfate dodecasaccharides reveal single sulfation site interconverts CXCL8 and CXCL12 chemokine biology. Chemical Communications (Cambridge, England). 51: 13846-9. PMID 26234943 DOI: 10.1039/C5Cc05222J |
0.485 |
|
2015 |
Baráth M, Hansen SU, Dalton CE, Jayson GC, Miller GJ, Gardiner JM. Modular synthesis of heparin-related tetra-, hexa- and octasaccharides with differential o-6 protections: programming for regiodefined 6-o-modifications. Molecules (Basel, Switzerland). 20: 6167-80. PMID 25859776 DOI: 10.3390/Molecules20046167 |
0.484 |
|
2015 |
Hansen SU, Dalton CE, Baráth M, Kwan G, Raftery J, Jayson GC, Miller GJ, Gardiner JM. Synthesis of L-iduronic acid derivatives via [3.2.1] and [2.2.2] L-iduronic lactones from bulk glucose-derived cyanohydrin hydrolysis: a reversible conformationally switched superdisarmed/rearmed lactone route to heparin disaccharides. The Journal of Organic Chemistry. 80: 3777-89. PMID 25646641 DOI: 10.1021/Jo502776F |
0.485 |
|
2014 |
Miller GJ, Hansen SU, Baráth M, Johannessen C, Blanch EW, Jayson GC, Gardiner JM. Synthesis of a heparin-related GlcN-IdoA sulfation-site variable disaccharide library and analysis by Raman and ROA spectroscopy. Carbohydrate Research. 400: 44-53. PMID 25457609 DOI: 10.1016/J.Carres.2014.06.026 |
0.494 |
|
2014 |
Jayson GC, Miller GJ, Hansen SU, Barath M, Gardiner JM, Avizienyte E. The development of anti-angiogenic heparan sulfate oligosaccharides. Biochemical Society Transactions. 42: 1596-600. PMID 25399576 DOI: 10.1042/Bst20140229 |
0.428 |
|
2013 |
Hansen SU, Miller GJ, Cole C, Rushton G, Avizienyte E, Jayson GC, Gardiner JM. Tetrasaccharide iteration synthesis of a heparin-like dodecasaccharide and radiolabelling for in vivo tissue distribution studies. Nature Communications. 4: 2016. PMID 23828390 DOI: 10.1038/Ncomms3016 |
0.494 |
|
2013 |
Takemoto N, Suehara T, Frisco HL, Sato S, Sezaki T, Kusamori K, Kawazoe Y, Park SM, Yamazoe S, Mizuhata Y, Inoue R, Miller GJ, Hansen SU, Jayson GC, Gardiner JM, et al. Small-molecule-induced clustering of heparan sulfate promotes cell adhesion. Journal of the American Chemical Society. 135: 11032-9. PMID 23822587 DOI: 10.1021/Ja4018682 |
0.425 |
|
2013 |
Hansen SU, Miller GJ, Jayson GC, Gardiner JM. First gram-scale synthesis of a heparin-related dodecasaccharide. Organic Letters. 15: 88-91. PMID 23240767 DOI: 10.1021/Ol303112Y |
0.51 |
|
2012 |
Hansen SU, Miller GJ, Baráth M, Broberg KR, Avizienyte E, Helliwell M, Raftery J, Jayson GC, Gardiner JM. Synthesis and scalable conversion of L-iduronamides to heparin-related di- and tetrasaccharides. The Journal of Organic Chemistry. 77: 7823-43. PMID 22900939 DOI: 10.1021/Jo300722Y |
0.483 |
|
2010 |
Miller GJ, Gardiner JM. Adaptable synthesis of C-glycosidic multivalent carbohydrates and succinamide-linked derivatization. Organic Letters. 12: 5262-5. PMID 20961035 DOI: 10.1021/Ol102310X |
0.454 |
|
2007 |
Conway SJ, Miller GJ. Biology-enabling inositol phosphates, phosphatidylinositol phosphates and derivatives. Natural Product Reports. 24: 687-707. PMID 17653355 DOI: 10.1039/B407701F |
0.424 |
|
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