2-Acetamido-2-deoxy-D-mannose
2-Acetamido-2-deoxy-D-mannose structure
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Common Name | 2-Acetamido-2-deoxy-D-mannose | ||
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| CAS Number | 7772-94-3 | Molecular Weight | 221.208 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 636.4±55.0 °C at 760 mmHg | |
| Molecular Formula | C8H15NO6 | Melting Point | 130ºC | |
| MSDS | Chinese USA | Flash Point | 338.7±31.5 °C | |
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A novel ion-exclusion chromatography–mass spectrometry method to measure concentrations and cycling rates of carbohydrates and amino sugars in freshwaters
J. Chromatogr. A. 1365 , 115-23, (2014) • Novel HPLC–MS method for carbohydrate and amino sugar analysis in freshwaters. • Rapid and efficient determination without derivatization or sample pre-concentration. • Implementation of stable isotope tracers to study compound biogeochemical cycling. • Glu... |
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First functional and mutational analysis of group 3 N-acetylneuraminate lyases from Lactobacillus antri and Lactobacillus sakei 23K.
PLoS ONE 9(5) , e96976, (2014) N-acetyl neuraminate lyases (NALs) catalyze the reversible aldol cleavage of N-acetyl neuraminic acid (Neu5Ac) to pyruvate and N-acetyl-D-mannosamine (ManNAc). Previous phylogenetic studies divided NALs into four different groups. Groups 1 and 2 have been wel... |
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Transport of N-acetyl-D-mannosamine and N-acetyl-D-glucosamine in Escherichia coli K1: effect on capsular polysialic acid production.
FEBS Lett. 511 , 97-101, (2002) N-Acetyl-D-mannosamine (ManNAc) and N-acetyl-D-glucosamine (GlcNAc) are the essential precursors of N-acetylneuraminic acid (NeuAc), the specific monomer of polysialic acid (PA), a bacterial pathogenic determinant. Escherichia coli K1 uses both amino sugars a... |