N-acetyl-alpha-D-galactosamine is a naturally occurring monosaccharide derivative that is found in various biological systems. It is a modified form of galactose, with an acetylated amino group attached to the C-2 position. N-acetyl-alpha-D-galactosamine plays important roles in various biological processes, including cell signaling, immune responses, and the synthesis of glycoproteins and glycolipids. The compound has been studied for its potential therapeutic applications, particularly in the treatment of certain types of cancer and inflammatory diseases. Its synthesis is often achieved through enzymatic methods, utilizing enzymes such as N-acetylgalactosaminyltransferases. The compound has been shown to exhibit anti-inflammatory effects, inhibit tumor cell growth, and modulate immune responses.'
N-acetyl-alpha-D-galactosamine : An N-acetyl-D-galactosamine having alpha-configuration at the anomeric centre. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]
ID Source | ID |
---|---|
PubMed CID | 84265 |
CHEMBL ID | 1230702 |
CHEBI ID | 40356 |
SCHEMBL ID | 262932 |
SCHEMBL ID | 21196403 |
Synonym |
---|
CHEBI:40356 , |
2-(acetylamino)-2-deoxy-alpha-d-galactopyranose |
CHEMBL1230702 |
n-acetyl-2-deoxy-2-amino-galactose |
a2g , |
2-acetamido-2-deoxy-alpha-d-galactopyranose |
tn saccharide component |
1AX0 , |
alpha-galnac |
tn antigen saccharide component |
galnac-alpha |
tn saccharide |
tn antigen saccharide |
n-acetyl-alpha-d-galactosamine |
alpha-galpnac |
DB03567 |
alpha-n-acetyl-d-galactosamine |
alpha-d-galactopyranose, 2-(acetylamino)-2-deoxy- |
n-[(2s,3r,4r,5r,6r)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide |
unii-00c01apn10 |
00c01apn10 , |
EPITOPE ID:141584 |
.alpha.-d-galactopyranose, 2-(acetylamino)-2-deoxy- |
SCHEMBL262932 |
2VMC |
3N35 |
n-acetyl-a-d-glucosamine |
2-acetamido-2-deoxy-.alpha.-d-galactose |
.alpha.-n-acetyl-d-galactosamine |
2-acetamido-2-deoxy-.alpha.-d-galactopyranose |
2-deoxy-2-acetamido-.alpha.-d-galactopyranose |
galactopyranose, 2-acetamido-2-deoxy-, .alpha.-d- |
2-(acetylamino)-2-deoxy-.alpha.-d-galactopyranose |
n-(2,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl)-acetamide,(n-acetyl-d- |
4OCQ |
AKOS030228287 |
AS-63026 |
alpha-2-acetamido-2-deoxy-delta-galactose |
2-acetylamino-2-deoxy-b-d-mannopyranose |
2-acetylamino-a-d-2-deoxy-glucose |
2-acetylamino-2-desoxy-a-d-mannose |
2-acetamino-2-desoxy-d-glucose |
2-acetylamino-2-deoxy-beta-delta-galactopyranose |
2-acetamido-2-deoxy-a-d-glucopyranose |
2-acetylamino-beta-d-2-deoxy-glucopyranose |
2-acetylamino-2-deoxy-beta-d-altropyranose |
2-acetylamino-delta-2-deoxy-mannose |
2-acetylamino-2-deoxy-beta-d-galactopyranose |
n-acetyl-delta-galactosamine |
2-acetylamino-2-deoxy-alpha-d-glucopyranose |
2-acetylamino-2-desoxy-beta-d-galaktose |
2-acetamino-2-deoxy-alpha-delta-glucose |
2-acetylamino-2-deoxy-alpha-d-galactopyranose |
2-acetylamino-2-desoxy-b-d-mannose |
2-acetylamino-2-deoxy-a-d-galactopyranose |
n-acetylglucosamin |
2-acetylamino-delta-2-deoxy-gulose |
2-acetylamino-beta-delta-2-deoxy-mannopyranose |
2-acetylamino-2-deoxy-alpha-delta-glucopyranose |
2-acetamido-2-desoxy-beta-delta-talofuranose |
2-acetylamino-d-2-deoxy-gulose |
2-acetylamino-2-deoxy-beta-d-allopyranose |
2-acetylamino-2-desoxy-alpha-delta-mannose |
2-acetylamino-alpha-d-2-deoxy-galactopyranose |
2-acetylamino-alpha-d-2-deoxy-glucose |
2-acetylamino-d-2-deoxy-talose |
2-acetamino-2-desoxy-delta-galaktose |
n-acetyl-alpha-delta-glucosamine |
2-acetylamino-2-deoxy-alpha-d-mannopyranose |
2-acetylamino-2-desoxy-a-d-galaktose |
2-acetylamino-l-2-deoxy-galactose |
2-acetylamino-2-deoxy-alpha-delta-galactopyranose |
2-acetamino-2-desoxy-a-d-glucopyranose |
2-acetylamino-alpha-delta-2-deoxy-galactopyranose |
2-acetylamino-2-deoxy-beta-d-mannopyranose |
2-acetylamino-2-desoxy-alpha-delta-galaktose |
2-acetylamino-d-2-deoxy-idose |
2-acetylamino-d-2-deoxy-mannose |
2-acetylamino-2-deoxy-alpha-delta-mannopyranose |
2-acetylamino-alpha-delta-2-deoxy-mannopyranose |
2-acetamido-2-deoxy-alpha-delta-glucopyranose |
2-acetylamino-2-desoxy-beta-delta-mannose |
alpha-2-acetamido-2-deoxy-d-galactose |
2-acetylamino-2-desoxy-delta-mannose |
2-acetamido-2-deoxy-b-d-glucopyranose |
2-acetamido-2-desoxy-beta-d-talofuranose |
2-acetamido-2-desoxy-b-d-talofuranose |
2-acetylamino-2-deoxy-b-d-glucopyranose |
2-acetylamino-l-2-deoxy-mannose |
2-acetylamino-2-deoxy-beta-delta-altropyranose |
n-acetyl-delta-allosamine |
2-acetamido-2-deoxy-alpha-d-allopyranose |
2-acetylamino-d-2-deoxy-galactose |
2-acetamino-2-desoxy-delta-glucose |
2-acetylamino-a-d-2-deoxy-glucopyranose |
2-acetylamino-2-deoxy-beta-delta-mannopyranose |
n-acetylgalactosamin |
2-acetylamino-alpha-d-2-deoxy-glucopyranose |
2-acetamino-2-deoxy-a-d-glucose |
2-acetylamino-2-desoxy-beta-delta-galaktose |
2-acetylamino-b-d-2-deoxy-galactopyranose |
2-acetylamino-b-d-2-deoxy-mannopyranose |
2-acetylamino-2-desoxy-beta-d-mannose |
2-acetylamino-2-desoxy-b-d-galaktose |
2-acetylamino-delta-2-deoxy-idose |
2-acetylamino-beta-delta-2-deoxy-glucopyranose |
2-acetylamino-beta-d-2-deoxy-mannopyranose |
2-acetylamino-2-deoxy-a-d-mannopyranose |
2-acetylamino-delta-2-deoxy-talose |
2-acetylamino-a-d-2-deoxy-galactopyranose |
2-acetamido-2-deoxy-a-d-allopyranose |
2-acetylamino-b-d-2-deoxy-glucopyranose |
2-acetylamino-2-deoxy-a-d-glucopyranose |
2-acetylamino-2-deoxy-beta-d-glucopyranose |
2-acetylamino-delta-2-deoxy-glucose |
2-acetylamino-2-deoxy-b-d-altropyranose |
2-acetylamino-beta-d-2-deoxy-galactopyranose |
2-acetylamino-2-deoxy-beta-delta-allopyranose |
2-acetylamino-2-deoxy-beta-delta-glucopyranose |
2-acetamido-2-deoxy-beta-delta-glucopyranose |
2-acetamino-2-desoxy-alpha-d-glucopyranose |
2-acetamino-2-desoxy-d-galaktose |
2-acetylamino-2-deoxy-b-d-galactopyranose |
2-acetamido-2-deoxy-alpha-delta-allopyranose |
2-acetylamino-delta-2-deoxy-galactose |
2-acetylamino-beta-delta-2-deoxy-galactopyranose |
2-acetylamino-2-desoxy-alpha-d-galaktose |
2-acetylamino-d-2-deoxy-glucose |
2-acetylamino-alpha-delta-2-deoxy-glucopyranose |
n-acetylgluosamin |
2-acetamino-2-deoxy-alpha-d-glucose |
2-acetylamino-a-d-2-deoxy-mannopyranose |
2-acetylamino-2-desoxy-d-mannose |
2-acetylamino-2-desoxy-dl-glucopyranose |
2-acetylamino-alpha-delta-2-deoxy-glucose |
2-acetylamino-2-desoxy-alpha-d-mannose |
2-acetamino-2-desoxy-alpha-delta-glucopyranose |
n-acetylmannosamin |
a-2-acetamido-2-deoxy-d-galactose |
a-d-galactopyranose,2-(acetylamino)-2-deoxy- |
n-((2s,3r,4r,5r,6r)-2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-3-yl)acetamide |
OVRNDRQMDRJTHS-CBQIKETKSA-N |
galnacalpha |
Q285835 |
SCHEMBL21196403 |
HY-128852 |
CS-0100924 |
n-?acetyl-?d-?galactosamine |
D71054 |
DTXSID70884733 |
Z1509640224 |
Role | Description |
---|---|
epitope | The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds. |
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Class | Description |
---|---|
N-acetyl-D-galactosamine | The D-enantiomer of N-acetylgalactosamine. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Chain A, Lectin | Erythrina corallodendron | Kd | 746.0000 | 515.0000 | 632.6667 | 746.0000 | AID977611 |
Chain A, Lectin | Erythrina corallodendron | Kd | 746.0000 | 515.0000 | 632.6667 | 746.0000 | AID977611 |
Chain A, Lectin | Erythrina corallodendron | Kd | 746.0000 | 515.0000 | 632.6667 | 746.0000 | AID977611 |
Chain A, Lectin | Erythrina corallodendron | Kd | 746.0000 | 515.0000 | 632.6667 | 746.0000 | AID977611 |
Chain A, Discoidin-2 | Dictyostelium discoideum AX2 | Kd | 1,150.0000 | 950.0000 | 1,050.0000 | 1,150.0000 | AID977611 |
Chain A, Discoidin-2 | Dictyostelium discoideum AX2 | Kd | 1,150.0000 | 950.0000 | 1,050.0000 | 1,150.0000 | AID977611 |
Chain A, Lectin | Erythrina corallodendron | Kd | 431.0000 | 431.0000 | 431.0000 | 431.0000 | AID977611 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1811 | Experimentally measured binding affinity data derived from PDB | 1998 | Journal of molecular biology, Apr-10, Volume: 277, Issue:4 | Structures of the Erythrina corallodendron lectin and of its complexes with mono- and disaccharides. |
AID977611 | Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB | 1998 | Journal of molecular biology, Apr-10, Volume: 277, Issue:4 | Structures of the Erythrina corallodendron lectin and of its complexes with mono- and disaccharides. |
AID1853212 | Drug uptake in human HepG2 cells with ASGPR overexpression assessed as fold increase in intracellular uptake | 2022 | RSC medicinal chemistry, Dec-14, Volume: 13, Issue:12 | Targeted protein degradation using the lysosomal pathway. |
AID977611 | Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB | 2008 | Proteins, Oct, Volume: 73, Issue:1 | Structure determination of Discoidin II from Dictyostelium discoideum and carbohydrate binding properties of the lectin domain. |
AID977611 | Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB | 2011 | Acta crystallographica. Section D, Biological crystallography, Mar, Volume: 67, Issue:Pt 3 | Modification of the sugar specificity of a plant lectin: structural studies on a point mutant of Erythrina corallodendron lectin. |
AID977611 | Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB | 2014 | Acta crystallographica. Section D, Biological crystallography, May, Volume: 70, Issue:Pt 5 | Insights into the binding specificity and catalytic mechanism of N-acetylhexosamine 1-phosphate kinases through multiple reaction complexes. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (13.07) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 1 (20.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 4 (80.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |