azides has been researched along with cellobiose in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lindhorst, T; MacLeod, AM; Warren, RA; Withers, SG | 1 |
| KAPLAN, JG | 1 |
| Gabra, N; Grandits, M; Holzer, W; Kracher, D; Ludwig, R; Mulla, D; Nagy, G; Saber, Y; Unger, FM; Viernstein, H | 1 |
| Guazzelli, L; Oscarson, S; Sheerin, K | 1 |
4 other study(ies) available for azides and cellobiose
| Article | Year |
|---|---|
The acid/base catalyst in the exoglucanase/xylanase from Cellulomonas fimi is glutamic acid 127: evidence from detailed kinetic studies of mutants.
Topics: Actinomycetales; Amino Acid Sequence; Azides; Base Sequence; beta-Glucosidase; Catalysis; Cellobiose; Cloning, Molecular; Disaccharides; Escherichia coli; Glucan 1,4-beta-Glucosidase; Glutamates; Glutamic Acid; Glycosylation; Hydrogen-Ion Concentration; Kinetics; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Sequence Alignment; Sodium Azide; Structure-Activity Relationship | 1994 |
AN INDUCIBLE SYSTEM FOR THE HYDROLYSIS AND TRANSPORT OF BETA-GLUCOSIDES IN YEAST. I. CHARACTERISTICS OF THE BETA-GLUCOSIDASE ACTIVITY OF INTACT AND OF LYSED CELLS.
Topics: Azides; beta-Glucosidase; Biological Transport; Carbohydrate Metabolism; Cellobiose; Cellulases; Glucose Oxidase; Glucosidases; Glucosides; Glycosides; Hydrolysis; Metabolism; Pharmacology; Research; Saccharomyces; Saccharomyces cerevisiae; Substrate Specificity; Temperature | 1965 |
Azido derivatives of cellobiose: oxidation at C1 with cellobiose dehydrogenase from Sclerotium rolfsii.
Topics: Ascomycota; Azides; Carbohydrate Dehydrogenases; Cellobiose; Chemistry Techniques, Synthetic; Kinetics; Lactones; Molecular Docking Simulation; Oxidation-Reduction; Protein Conformation; Substrate Specificity | 2013 |
Large scale synthesis and regioselective protection schemes of ethyl 2-azido-2-deoxy-1-thio-α-d-cellobioside for preparation of heparin thiodisaccharide building blocks.
Topics: Azides; Benzyl Compounds; Carbohydrate Conformation; Carbohydrate Sequence; Cellobiose; Disaccharides; Heparin; Heparitin Sulfate; Magnetic Resonance Spectroscopy; Nitro Compounds; Oxidation-Reduction; Stereoisomerism; Sulfhydryl Compounds | 2017 |