This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration. This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration.

N-Acetyl-D-Glucosamine

PubChem CID: 439174

Connections displayed (default: 10).
Loading graph...

Compound Synonyms N-acetyl-D-glucosamine, GlcNAc, 2-acetamido-2-deoxy-D-glucopyranose, 2-Acetamido-2-deoxy-D-glucose, D-GlcNAc, n-acetyl-glucosamine, 2-acetamido-2-deoxy-glucose, 2-Deoxy-2-Acetamido-Glucose, 2-Deoxy-2-Acetamido-D-Glucose, 2-Acetamido-2-Deoxy-Glucopyranose, 2-Deoxy-2-Acetamido-Glucopyranose, 2-acetamido-2-deoxy-glucopyranoside, 2-Deoxy-2-Acetamido-Glucopyranoside, 2-Deoxy-2-Acetamido-D-Glucopyranose, 2-acetamido-2-deoxy-D-glucopyranoside, 2-Deoxy-2-Acetamido-D-Glucopyranoside, N-Acetylchitosamine, acetylglucosamine, CHEBI:506227, N-((3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide, N-Acetyl-D-glucosamine-Agarose, NAcGlc, N-[(3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide, 72-87-7, N-Acetyl Glucosamine, SMR000857242, N-Acetyl-2-amino-2-deoxy-D-glucose, 2-(Acetylamino)-2-deoxyhexopyranose #, 2-Deoxy-2-(acetylamino)-D-glucopyranose, Epitope ID:137340, MLS001333127, MLS001333128, SCHEMBL468802, 2-(Acetylamino)-2-deoxyhexose, CHEMBL240524, N-Acetylglucosamine cyclized form, DTXCID30820152, DTXSID901045903, HMS2230N05, N-Acetyl-D-glucosamine, >=99%, 2-acetamido-2-deoxy-d-glu-copyranose, 2-Acetamido-2-deoxy -D-glucopyranose, AKOS015914726, N-Acetyl-D-glucosamine, >=95% (HPLC), A0092, CS-0326546, C00140, EN300-19632131, N-acetyl-D-glucosamine (incomplete stereochemistry), Q27225758, N_FULL/O_FULL_01000000000000_GS_1219, N-Acetyl-D-glucosamine, suitable for cell culture, BioReagent, WURCS=2.0/1,1,0/(a2122h-1x_1-5_2*NCC/3=O)/1/, N-Acetylglucosamine, United States Pharmacopeia (USP) Reference Standard, N-((3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)-tetrahydro-2H-pyran-3-yl)acetamide, N-Acetylglucosamine, Pharmaceutical Secondary Standard, Certified Reference Material
Topological Polar Surface Area 119.0
Hydrogen Bond Donor Count 5.0
Inchi Key OVRNDRQMDRJTHS-RTRLPJTCSA-N
Rotatable Bond Count 2.0
State Solid
Substituent Name Acylaminosugar, N-acyl-alpha-hexosamine, Oxane, Monosaccharide, Acetamide, Secondary carboxylic acid amide, Secondary alcohol, Polyol, Hemiacetal, Carboxamide group, 1,2-diol, Oxacycle, Organoheterocyclic compound, Ether, Carboxylic acid derivative, Carboxylic acid amide, Hydrocarbon derivative, Primary alcohol, Organonitrogen compound, Carbonyl group, Alcohol, Aliphatic heteromonocyclic compound
Synonyms 2-(Acetylamino)-2-deoxyglucose, 9CI, 2-(acetylamino)-2-Deoxyhexose, 2-acetamido-2-Deoxy-D-glucopyranose, 2-acetamido-2-Deoxy-D-glucose, 2-acetamido-2-Deoxyglucose, 2-acetamido-D-Glucose, 2-acetylamino-2-Deoxy-D-glucose, Acetylglucosamine, GlcNAc, N-[(3R,4R,5S,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide, N-Acetyl-D-glucosamine, N-Acetylchitosamine, N-Acetylglucosamine, 2-Acetamido-2-deoxy-D-glucose, 2-(Acetylamino)-2-deoxyhexose, 2-Acetamido-2-deoxy-D-glucopyranose, 2-Acetamido-2-deoxyglucose, 2-Acetamido-D-glucose, 2-Acetylamino-2-deoxy-D-glucose, 2 Acetamido 2 deoxyglucose, N Acetyl D glucosamine, 2 Acetamido 2 deoxy D glucose
Heavy Atom Count 15.0
Pathway Kegg Map Id map00520
Compound Name N-Acetyl-D-Glucosamine
Kingdom Organic compounds
Description Monomer of Chitinand is also in the exopolysaccharide from blue-green alga Cyanospira capsulata (CCD) N-Acetylglucosamine (N-acetyl-D-glucosamine, or GlcNAc, or NAG) is a monosaccharide derivative of glucose. It is part of a biopolymer in the bacterial cell wall, built from alternating units of GlcNAc and N-acetylmuramic acid (MurNAc), cross-linked with oligopeptides at the lactic acid residue of MurNAc. GlcNAc is the monomeric unit of the polymer chitin, which forms the outer coverings of insects and crustaceans. N-Acetylglucosamine is found in peach.
Exact Mass 221.09
Formal Charge 0.0
Monoisotopic Mass 221.09
Isotope Atom Count 0.0
Molecular Complexity 235.0
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 221.21
Database Name fooddb_chem_all;hmdb_chem_all;npass_chem_all;pubchem
Covalent Unit Count 1.0
Enzyme Uniprot Id Q9Y223, P51606, P07686, P06865, Q9UJ70, Q9BZP6, Q9UK23, Q13231, P54802, P61626, Q6UWQ5, Q7Z4W2, Q96QH8, O75951
Uniprot Id Q9Y223, P51606, O60909, P15291, P07686, P06865, Q9UJ70, Q9BZP6, Q9UK23, Q13231, O60512, O60513, P54802, P61626, Q8WZA1, Q6UWQ5, Q7Z4W2, Q96QH8, O75951, P36222, Q15782, Q8WVB3, O60502, Q6P4F1, P00811, O75874, P27695, Q8N539
Defined Atom Stereocenter Count 4.0
Iupac Name N-[(3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
Total Atom Stereocenter Count 5.0
Molecular Framework Aliphatic heteromonocyclic compounds
Total Bond Stereocenter Count 0.0
Class Carbohydrates and carbohydrate conjugates
Inchi InChI=1S/C8H15NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6-,7-,8?/m1/s1
Smiles CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](OC1O)CO)O)O
Xlogp -1.7
Superclass Organooxygen compounds
Defined Bond Stereocenter Count 0.0
Subclass Aminosaccharides
Taxonomy Direct Parent Acylaminosugars
Molecular Formula C8H15NO6

  • 1. Outgoing r'ship FOUND_IN to/from Prunus Persica (Plant) Rel Props:Source_db:fooddb_chem_all