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N-Acetylneuraminic Acid


CAS: 131-48-6

Chemical Formula: C11H19NO9

Molecular Weight: 309.27

Appearance: Amorphous White Powder

Synonyms:
5-(Acetylamino)-3,5-dideoxy-D-glycero-D-galacto-2-nonulosonic Acid; NANA; N-Acetylsialic Acid; Sialic Acid; 

References:
1. "A functional model of sialo-glyco-macromolecules in synaptic transmission and memory formation" Rahmann, H.; Rosner, H.; Breer, H. J. Theor. Biol. 1976, 57, 231.

2. "A first synthesis of sulfonic acid analogues of N-acetylneuraminic acid" Z. B. Szabo ´ et al. / Tetrahedron Letters 49 (2008) 1196–1198 Full text

3. Sugahara, K.; Sugimoto, K.; Nomura, O.; Usui, T. Clin. Chim. Acta 1980, 108, 493.

4. Kolisis, F. N. Biotechnol. Appl. Biochem. 1986, 8, 148.

5. Resende, R.; Glover, C.; Watts, A. G. Tetrahedron Lett. 2009, 50, 4009.

6.  Von Itzstein, M.; Wu, W.-Y.; Jin, B. Carbohydr. Res. 1994, 259, 301.

7. Eisenberg, E. J.; Bidgood, A.; Cundy, K. C. Antimicrob. Agents Chemother. 1997, 41, 1949.

8. Wiggins, R.; Crowley, T.; Horner, P. J.; Soothill, P. W.; Millar, M. R.; Corfield, A. P. J. Clin. Microbiol. 2000, 38, 3096.

9. Boons, G.-J.; Demchenko, A. V. Chem. Rev. 2000, 100, 4539.

10. "Rare-Earth Metal Triflates in Organic Synthesis" Kobayashi, S.; Sugiura, M.; Kitagawa, H.; Lam, W. W. L. Chem. Rev. 2002, 102, 2227. Full text

11, "Novel glycosylation reactions using glycosyl thioimidates of N-acetylneuraminic acid as sialyl donors." Kiyoshi Ikeda et al.:Bioorganic & Medicinal Chemistry Letters 16 (2006) 2618–2620 Full text

 

The product is only for R&D purpose,not for human use.We will not take any responsibility for illegal use.

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