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Page 1
Sialylation of glycoprotein oligosaccharides with N-acetyl-, N-glycolyl-, and N-O-diacetylneuraminic acids.
Higa HH, Paulson JC. Higa HH, et al. J Biol Chem. 1985 Jul 25;260(15):8838-49. J Biol Chem. 1985. PMID: 4019457 Free article.
Four common sialic acids (Sia), NeuAc, N-glycolyl-neuraminic acid (NeuGc), 4-O-acetyl-N-acetylneuraminic acid (4-O-Ac-NeuAc), and 9-O-Ac-NeuAc were examined for activation to their corresponding CMP-sialic acid conjugates and subsequently …
Four common sialic acids (Sia), NeuAc, N-glycolyl-neuraminic acid (NeuGc), 4-O-acetyl-N-acetylneuraminic …
Identification by gas-liquid chromatography-mass spectrometry of 4-O-acetyl-9-O-lactyl-N-acetyl-neuraminic acid, a new sialic acid from horse submandibular gland.
Reuter G, Pfeil R, Kamerling JP, Vliegenthart JF, Schauer R. Reuter G, et al. Biochim Biophys Acta. 1980 Jun 19;630(2):306-10. doi: 10.1016/0304-4165(80)90435-3. Biochim Biophys Acta. 1980. PMID: 7388057
The novel sialic acid 4-O-acetyl-9-O-lactyl-N-acetylneuraminic acid has been identified as a constituent of horse submandibular gland glycoproteins in addition to the already known equine sialic acids, N-acetylneuraminic acid, 4-O-acetyl-N-acetylneu …
The novel sialic acid 4-O-acetyl-9-O-lactyl-N-acetylneuraminic acid has been identified as a constituent of horse submandibular gland glycop …
Unique disialosyl gangliosides from salmon kidney: characterization of V3alphaFuc, IV3betaGalNAc, II3(alphaNeuAc)2-Gg4Cer and its analogue with 4-O-acetyl-N-acetylneuraminic acid.
Niimura Y, Ishizuka I. Niimura Y, et al. Glycoconj J. 2006 Nov;23(7-8):489-99. doi: 10.1007/s10719-006-6562-1. Glycoconj J. 2006. PMID: 17006641
NMR showed that X3 and X4 were analogues of X5 and X6 and contained O-acetyl groups on C4 of the outer N-acetylneuraminic acid, first disialosyl gangliosides containing 4-O-acetyl-N-acetylneuraminic acid. The ceramides of X3 and X5 contai …
NMR showed that X3 and X4 were analogues of X5 and X6 and contained O-acetyl groups on C4 of the outer N-acetylneuraminic acid, first disial …
Analysis of N-acetyl-4-O-acetylneuraminic-acid-containing N-linked carbohydrate chains released by peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase F. Application to the structure determination of the carbohydrate chains of equine fibrinogen.
Damm JB, Voshol H, Hård K, Kamerling JP, Vliegenthart JF. Damm JB, et al. Eur J Biochem. 1989 Mar 1;180(1):101-10. doi: 10.1111/j.1432-1033.1989.tb14620.x. Eur J Biochem. 1989. PMID: 2707257 Free article.
Basis for the potent inhibition of influenza virus infection by equine and guinea pig alpha 2-macroglobulin.
Pritchett TJ, Paulson JC. Pritchett TJ, et al. J Biol Chem. 1989 Jun 15;264(17):9850-8. J Biol Chem. 1989. PMID: 2470765 Free article.
The inhibitory activities of both sera are found to reside entirely in their respective alpha 2-macroglobulins, high molecular weight glycoproteins which bind to viral hemagglutinins via sialic acids of their N-linked carbohydrate groups. Structure analysis has shown that both pr …
The inhibitory activities of both sera are found to reside entirely in their respective alpha 2-macroglobulins, high molecular weight glycop …
Substiuted sialic acid prosthetic groups as determinants of viral hemagglutination.
Levinson B, Pepper D, Belyavin G. Levinson B, et al. J Virol. 1969 May;3(5):477-83. doi: 10.1128/JVI.3.5.477-483.1969. J Virol. 1969. PMID: 4306720 Free PMC article.
Using selected reagents, it was demonstrated that the active substituent on the horse serum inhibitor of A2 influenza virus was 4-O-acetyl-N-acetylneuraminic acid; however, the active substituent on the inhibitor of the influenza B virus …
Using selected reagents, it was demonstrated that the active substituent on the horse serum inhibitor of A2 influenza virus was 4- …