All journal publications (1963-2013)
Filters: keyword is inhibitor [Clear All Filters]
- 2012
The Development of an Aza-C-Glycoside Library Based on a Tandem Staudinger/Aza-Wittig/Ugi Three-Component Reaction,
European Journal of Organic Chemistry, no. 32, pp. 6420-6454.
Novel Activity-Based Probes for Broad-Spectrum Profiling of Retaining beta-Exoglucosidases In Situ and In Vivo,
Angewandte Chemie-International Edition, vol. 51, no. 50, pp. 12529-12533.
Tuning the leaving group in 2-deoxy-2-fluoroglucoside results in improved activity-based retaining beta-glucosidase probes,
Chemical Communications, vol. 48, no. 84, pp. 10386-10388.
- 2011
Bioorthogonal Chemistry: Applications in Activity-Based Protein Profiling,
Accounts of Chemical Research, vol. 44, no. 9, pp. 718-729.
The natural product hybrid of Syringolin A and Glidobactin A synergizes proteasome inhibition potency with subsite selectivity,
Chem Commun (Camb), vol. 47, no. 1, pp. 385-7. DOI
- 2010
Incorporation of Fluorinated Phenylalanine Generates Highly Specific Inhibitor of Proteasome's Chymotrypsin-like Sites,
Journal of Medicinal Chemistry, vol. 53, no. 5, pp. 2319-2323. DOI
Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism,
European Journal of Organic Chemistry, no. 7, pp. 1258-1283. DOI
Nanomolar affinity, iminosugar-based chemical probes for specific labeling of lysosomal glucocerebrosidase,
Bioorganic & Medicinal Chemistry, vol. 18, no. 1, pp. 267-273. DOI
- 2009
O-GlcNAc Peptide Epoxyketones Are Recognized by Mammalian Proteasomes,
Journal of the American Chemical Society, vol. 131, no. 34, pp. 12064-+. DOI
Syringolin A Selectively Labels the 20 S Proteasome in Murine EL4 and Wild-Type and Bortezomib-Adapted Leukaemic Cell Lines,
Chembiochem, vol. 10, no. 16, pp. 2638-2643. DOI
Characterization of the ubiquitin-proteasome system in bortezomib-adapted cells,
Leukemia, vol. 23, no. 6, pp. 1098-1105. DOI
Chemical Tools To Study the Proteasome,
European Journal of Organic Chemistry, no. 20, pp. 3301-3313. DOI
Functional Proteomics on Zinc-Dependent Metalloproteinases using Inhibitor Probes,
Chemmedchem, vol. 4, no. 2, pp. 164-170. DOI
Synthesis and evaluation of D-gluco-pyranocyclopropyl amines as potential glucosidase inhibitors,
Bioorganic & Medicinal Chemistry Letters, vol. 19, no. 23, pp. 6600-6603. DOI
A peptide hydroxamate library for enrichment of metalloproteinases: towards an affinity-based metalloproteinase profiling protocol,
Org Biomol Chem, vol. 6, no. 7, pp. 1244-50. DOI
Glycosphingolipids-Nature, Function, and Pharmacological Modulation,
Angewandte Chemie-International Edition, vol. 48, no. 47, pp. 8848-8869. DOI
- 2008
Reciprocal chemical genetics for swift lead and target identification,
Molecular Biosystems, vol. 4, no. 10, pp. 1001-1008. DOI
Azido-BODIPY acid reveals quantitative Staudinger-Bertozzi ligation in two-step activity-based proteasome profiling,
Chembiochem, vol. 9, no. 11, pp. 1735-1738. DOI
Ritonavir induces endoplasmic reticulum stress and sensitizes sarcoma cells toward bortezomib-induced apoptosis,
Molecular Cancer Therapeutics, vol. 7, no. 7, pp. 1940-1948. DOI
A peptide hydroxamate library for enrichment of metalloproteinases: towards an affinity-based metalloproteinase profiling protocol,
Organic & Biomolecular Chemistry, vol. 6, no. 7, pp. 1244-1250. DOI
- 2007
A compendium of sugar amino acids (SAA): scaffolds, peptide- and glyco-mimetics,
Tetrahedron-Asymmetry, vol. 18, no. 17, pp. 2001-2010. DOI
A cell-permeable inhilbitor and activity-based probe for the caspase-like activity of the proteasome,
Bioorganic & Medicinal Chemistry Letters, vol. 17, no. 12, pp. 3402-3405. DOI
Fragment-based synthesis and SAR of modified FKBP ligands: Influence of different linking on binding affinity,
Chemmedchem, vol. 2, no. 7, pp. 1054-1070. DOI
Activity patterns of proteasome subunits reflect bortezomib sensitivity of hematologic malignancies and are variable in primary human leukemia cells,
Leukemia, vol. 21, no. 1, pp. 84-92.
Synthesis of alkylated sugar amino acids: conformationally restricted L-Xaa-L-Ser/Thr mimics,
Organic & Biomolecular Chemistry, vol. 5, no. 14, pp. 2311-2314. DOI


