19700 <common-name>N-Acetylglucosamine</common-name> <description>N-Acetylglucosamine is an organic compound with the formula C8H15NO6 and an average molecular weight of 221.21 g/mol. N-Acetylglucosamine belongs to the carbohydrates and carbohydrate conjugates, a subclass of organooxygen compounds within the organic compounds. This compound is found in or released from ten recorded sources. These include electrical and electronic equipment, specifically amplifiers, television systems, loudspeakers, line transmission systems, adjustable resistors, and one additional source. It is also associated with food, food processing, and cookware, including the processing of fish, the preparation of vinegar, the preparation of wine or sparkling wine, and molasses and the treatment of molasses. N-Acetylglucosamine interacts with six recorded protein targets. It acts as an activator of Alpha-N-acetylglucosaminidase (NAGLU) and targets N-acylglucosamine 2-epimerase (RENBP), Beta-1,4-galactosyltransferase 1 (B4GALT1), and Beta-1,4-galactosyltransferase 4 (B4GALT4), along with two other proteins.</description> <cas>7512-17-6</cas> <pubchem-id>343911</pubchem-id> <chemical-formula>C8H15NO6</chemical-formula> <weight>221.21</weight> <appearance nil="true"/> <melting-point nil="true"/> <boiling-point nil="true"/> <density nil="true"/> <solubility nil="true"/> <specific-gravity nil="true"/> <flash-point nil="true"/> <vapour-pressure nil="true"/> <route-of-exposure nil="true"/> <target nil="true"/> <mechanism-of-toxicity nil="true"/> <metabolism nil="true"/> <toxicity nil="true"/> <lethaldose nil="true"/> <carcinogenicity nil="true"/> <use-source nil="true"/> <min-risk-level nil="true"/> <health-effects nil="true"/> <symptoms nil="true"/> <treatment nil="true"/> <created-at type="dateTime">2016-05-22T05:22:10Z</created-at> <updated-at type="dateTime">2026-08-24T16:32:16Z</updated-at> <interacting-proteins nil="true"/> <wikipedia nil="true"/> <uniprot-id nil="true"/> <kegg-compound-id nil="true"/> <omim-id nil="true"/> <chebi-id nil="true"/> <biocyc-id nil="true"/> <ctd-id nil="true"/> <stitch-id nil="true"/> <drugbank-id>DB00141</drugbank-id> <pdb-id nil="true"/> <actor-id nil="true"/> <organism nil="true"/> <export type="boolean">true</export> <metabolizing-proteins nil="true"/> <transporting-proteins nil="true"/> <moldb-smiles>[H]C(=O)[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@H](O)CO</moldb-smiles> <moldb-formula>C8H15NO6</moldb-formula> <moldb-inchi>InChI=1S/C8H15NO6/c1-4(12)9-5(2-10)7(14)8(15)6(13)3-11/h2,5-8,11,13-15H,3H2,1H3,(H,9,12)/t5-,6+,7+,8+/m0/s1</moldb-inchi> <moldb-inchikey>MBLBDJOUHNCFQT-LXGUWJNJSA-N</moldb-inchikey> <moldb-average-mass type="decimal">221.2078</moldb-average-mass> <moldb-mono-mass type="decimal">221.089937217</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>-3.9</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id nil="true"/> <structure-image-file-name nil="true"/> <structure-image-content-type nil="true"/> <structure-image-file-size type="integer" nil="true"/> <structure-image-updated-at type="dateTime" nil="true"/> <biodb-id nil="true"/> <synthesis-reference nil="true"/> <structure-image-caption nil="true"/> <chemdb-id>CHEM018595</chemdb-id> <dsstox-id>DTXSID3045855</dsstox-id> <toxcast-id>45855</toxcast-id> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id nil="true"/> <iupac>N-[(2R,3R,4S,5R)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl]acetamide</iupac> <moldb-polar-surface-area>127.09</moldb-polar-surface-area> <moldb-refractivity>48.4469</moldb-refractivity> <moldb-polarizability>20.489506839444218</moldb-polarizability> <moldb-rotatable-bond-count>6</moldb-rotatable-bond-count> <moldb-acceptor-count>6</moldb-acceptor-count> <moldb-donor-count>5</moldb-donor-count> <moldb-pka-strongest-acidic>11.564821144474056</moldb-pka-strongest-acidic> <moldb-pka-strongest-basic>-1.1597845911248257</moldb-pka-strongest-basic> <moldb-physiological-charge>0</moldb-physiological-charge> <moldb-number-of-rings>0</moldb-number-of-rings> <moldb-alogps-logp>-2.10</moldb-alogps-logp> <moldb-alogps-logs>-0.18</moldb-alogps-logs> <moldb-alogps-solubility>1.48e+02 g/l</moldb-alogps-solubility> <kingdom>Organic compounds</kingdom> <superklass>Organic oxygen compounds</superklass> <klass>Organooxygen compounds</klass> <subklass>Carbohydrates and carbohydrate conjugates</subklass> <paper-count type="integer">12920</paper-count> <sync-id>CED0001371</sync-id> <structure-inchikey>MBLBDJOUHNCFQT-LXGUWJNJSA-N</structure-inchikey> 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type="dateTime">2026-09-19T04:07:44Z</structure-indexed-at> </compound>