Chemistry:N-Acetylgalactosamine
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Revision as of 04:25, 30 June 2021 by imported>WikiG (fix)
Short description: Chemical compound
Names | |
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IUPAC name
2-(Acetylamino)-2-deoxy-D-galactose
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Other names
GalNAc; 2-Acetamido-2-deoxy-D-galactose; N-Acetylchondrosamine; 2-Acetamido-2-deoxy-D-galactopyranose; N-Acetyl-D-galactosamine
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Identifiers | |
3D model (JSmol)
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ChEBI | |
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DrugBank | |
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PubChem CID
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UNII | |
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Properties | |
C8H15NO6 | |
Molar mass | 221.21 g/mol |
Melting point | 172 to 173 °C (342 to 343 °F; 445 to 446 K) |
Related compounds | |
Related monosaccharides
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N-Acetylglucosamine Galactosamine Galactose |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Tracking categories (test):
N-Acetylgalactosamine (GalNAc), is an amino sugar derivative of galactose.
Function
In humans it is the terminal carbohydrate forming the antigen of blood group A.[1]
It is typically the first monosaccharide that connects serine or threonine in particular forms of protein O-glycosylation.
N-Acetylgalactosamine is necessary for intercellular communication, and is concentrated in sensory nerve structures of both humans and animals.
GalNAc is also used as a targeting ligand in investigational antisense oligonucleotides and siRNA therapies targeted to the liver, where it binds to the asialoglycoprotein receptors on hepatocytes. [2]
See also
- Galactosamine
- Globoside
- (N-Acetylglucosamine) GlcNAc
References
- ↑ Donald M. Marcus; Elvin A. Kabat; Gerald Schiffman (1964). "Immunochemical Studies on Blood Groups. XXXI. Destruction of Blood Group A Activity by an Enzyme from Clostridium tertium Which Deacetylates N-Acetylgalactosamine in Intact Blood Group Substances". Biochemistry 3 (3): 437–443. doi:10.1021/bi00891a023.
- ↑ Nair, Jayaprakash K; Willoughby, Jennifer L. S; Chan, Amy; Charisse, Klaus; Alam, Md. Rowshon; Wang, Qianfan; Hoekstra, Menno; Kandasamy, Pachamuthu et al. (2014). "Multivalent N-Acetylgalactosamine-Conjugated siRNA Localizes in Hepatocytes and Elicits Robust RNAi-Mediated Gene Silencing". Journal of the American Chemical Society 136 (49): 16958–16961. doi:10.1021/ja505986a. PMID 25434769. http://www.escholarship.org/uc/item/54c114pc.
External links
Original source: https://en.wikipedia.org/wiki/N-Acetylgalactosamine.
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