Cytidine Monophosphate N-Acetylneuraminic Acid
"Cytidine Monophosphate N-Acetylneuraminic Acid" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A nucleoside monophosphate sugar which donates N-acetylneuraminic acid to the terminal sugar of a ganglioside or glycoprotein.
|Cytidine Monophosphate N-Acetylneuraminic Acid
- Cytidine Monophosphate N-Acetylneuraminic Acid
- Cytidine Monophosphate N Acetylneuraminic Acid
- CMP Acetylneuraminic Acid
- Acetylneuraminic Acid, CMP
- Acid, CMP Acetylneuraminic
- CMP-Sialic Acid
- Acid, CMP-Sialic
- CMP Sialic Acid
Below are MeSH descriptors whose meaning is more general than "Cytidine Monophosphate N-Acetylneuraminic Acid".
Below are MeSH descriptors whose meaning is more specific than "Cytidine Monophosphate N-Acetylneuraminic Acid".
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Below are the most recent publications written about "Cytidine Monophosphate N-Acetylneuraminic Acid" by people in Profiles.
Gulati S, Schoenhofen IC, Lindhout-Djukic T, Schur MJ, Landig CS, Saha S, Deng L, Lewis LA, Zheng B, Varki A, Ram S. Therapeutic CMP-Nonulosonates against Multidrug-Resistant Neisseria gonorrhoeae. J Immunol. 2020 06 15; 204(12):3283-3295.
Gulati S, Schoenhofen IC, Whitfield DM, Cox AD, Li J, St Michael F, Vinogradov EV, Stupak J, Zheng B, Ohnishi M, Unemo M, Lewis LA, Taylor RE, Landig CS, Diaz S, Reed GW, Varki A, Rice PA, Ram S. Utilizing CMP-Sialic Acid Analogs to Unravel Neisseria gonorrhoeae Lipooligosaccharide-Mediated Complement Resistance and Design Novel Therapeutics. PLoS Pathog. 2015 Dec; 11(12):e1005290.
Gulati S, Sastry K, Jensenius JC, Rice PA, Ram S. Regulation of the mannan-binding lectin pathway of complement on Neisseria gonorrhoeae by C1-inhibitor and alpha 2-macroglobulin. J Immunol. 2002 Apr 15; 168(8):4078-86.
Simon ES, Toone EJ, Ostroff G, Bednarski MD, Whitesides GM. Preparation of cytidine 5'-monophospho-N-acetylneuraminic acid and uridine 5'-diphosphoglucuronic acid; syntheses of alpha-2, 6-sialyllactosamine, alpha-2, 6-sialyllactose, and hyaluronic acid. Methods Enzymol. 1989; 179:275-87.