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Neu5Ac

Acetamido-3,5-dicleoxy-D-g/ycero-a-D gafacfo-non-2-ulopyranosonic acid (W-acetyl-a-neuraminic acid, a-Neu5Ac), drawn in three ways (note that C-7 is the anomeric reference atom)... [Pg.85]

Cytidine 5 -(5-acetamido-3,5-dideoxy-D-g/ycero-P-D-ga/acto-non-2-ulopyranosylonic acid monophosphate) (CMP-p-Neu5Ac)... [Pg.115]

Fig. 1 A view of the influenza virus haemagglutinin (HA) monomer with the receptor fragment a-2,3-sialyUactose [a-Neu5Ac-(2,3)- 3-Gal-(1,4)-P-Glc] bound... Fig. 1 A view of the influenza virus haemagglutinin (HA) monomer with the receptor fragment a-2,3-sialyUactose [a-Neu5Ac-(2,3)- 3-Gal-(1,4)-P-Glc] bound...
F%.2 A view of the influenza vims sialidase (NA) monomer with a-Neu5Ac 3a bound in the active site... [Pg.114]

The discovery of the potent in vitro sialidase inhibitory activity and in vivo efficacy of zanamivir 12, and the increasing availability of 3D structural data for influenza virus sialidases in the 1990s, particularly with Neu5Ac and various inhibitors bound into the active site, provided a platform for further drug discovery efforts targeting... [Pg.123]

Chan T-H, Xin Y-C, von Itzstein M (1997) Synthesis of phosphonic add analogs of siaUc acids (Neu5Ac and KDN) as potential sialidase inhibitors. J Org Chem 62 3500-3504 Chand P, Kotian PL, Dehghani A, El-Kattan Y, Lin T-H, Hutchison TL, Babu YS, Bantia S, Elliott AJ, Montgomery JA (2001) Systematic structure-based design and stereoselective synthesis of novel multisubstituted cyclopentane derivatives with potent antiinfluenza activity. J Med Chem 44 4379 392... [Pg.146]

Aldulosonic acids are involved in many important areas of glycobiology and glycomedicine, such as /V-acetylneuraminic acid (Neu5Ac), 3-deoxy-D-glycero-v-galacto-non-2- Aosonic acid (Kdn) and 3-deoxy-D-manno-oct-2-ulosonic acid (Kdo). [Pg.92]

Sialic acid Neu5Ac Flu virus Limax flavus 13-15... [Pg.362]

PAMAM-Chitosan 29a-e DS (NH2) Sialoside hybrid DS (Neu5Ac) Reactivity (%r... [Pg.381]

Finally, saponification of 26 followed by acid treatment (Dowex resin) afforded racemic NeuSAc, whose NMR spectrum (490 MHz) and chromatographic properties were identical with those of authentic NeuSAc. An efficient and stereoselective total synthesis of Neu5Ac had been accomplished as shown in Figure 6. [Pg.169]

UDP-a-D-Gal UDP-a-D-GlcNAc UDP-a-D-GalNAc GDP-a-D-Man GDP-P-l-Fuc CMP-Neu5Ac dTDP-a-D-Glc, dTDP-P-L-Rha combinatorial biocatalysis [32]... [Pg.87]


See other pages where Neu5Ac is mentioned: [Pg.160]    [Pg.116]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.118]    [Pg.119]    [Pg.125]    [Pg.142]    [Pg.143]    [Pg.143]    [Pg.35]    [Pg.35]    [Pg.85]    [Pg.216]    [Pg.217]    [Pg.276]    [Pg.92]    [Pg.93]    [Pg.111]    [Pg.304]    [Pg.362]    [Pg.362]    [Pg.371]    [Pg.381]    [Pg.74]    [Pg.35]    [Pg.160]    [Pg.160]    [Pg.163]    [Pg.175]    [Pg.176]    [Pg.176]    [Pg.178]    [Pg.90]    [Pg.90]    [Pg.92]    [Pg.94]   


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7-Amino-substituted Neu5Ac derivative

CMP-Neu5Ac hydroxylase

CMP-Neu5Ac-synthetase

CMP-p-Neu5Ac

Deaminated Neu5Ac analogues preparation

Enzyme Neu5Ac-aldolase

Formation of Neu5Ac

HA inhibitors Neu5Ac-P2Me methyl ester

HA inhibitors Neu5Ac-a2Me amide

HA inhibitors Neu5Ac-a2Me benzyl este

HA inhibitors Neu5Ac-a2Me methyl este

Neu5Ac aldolase

Neu5Ac aldolase catalysis synthesis of KDO

Neu5Ac aldolase isolation

Neu5Ac analogs

Neu5Ac analogs preparation

Neu5Ac anomers

Neu5Ac precursor

Neu5Ac structure

Neu5Ac transferase

Neu5Ac-synthetase

Sugar derived heptosyl bromide in Neu5Ac synthesis

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