N-beta-D-glucopyranosylacetamide (CHEM128429)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-13 21:30:27 UTC | ||||||||
| Update Date | 2026-05-14 17:34:22 UTC | ||||||||
| Accession Number | CHEM128429 | ||||||||
| Identification | |||||||||
| Common Name | N-beta-D-glucopyranosylacetamide | ||||||||
| Class | Small Molecule | ||||||||
| Description | N-beta-D-glucopyranosylacetamide is an organic compound with the formula C8H15NO6 and an average molecular weight of 221.21 g/mol. N-beta-D-glucopyranosylacetamide belongs to the carbohydrates and carbohydrate conjugates, a subclass of organooxygen compounds within the organic compounds. This compound acts as an inhibitor of two protein targets: the liver form of glycogen phosphorylase (PYGL) and the muscle form of glycogen phosphorylase (PYGM). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C8H15NO6 | ||||||||
| Average Molecular Mass | 221.208 g/mol | ||||||||
| Monoisotopic Mass | 221.090 g/mol | ||||||||
| CAS Registry Number | 6983-36-4 | ||||||||
| IUPAC Name | N-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]acetamide | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | [H]N([C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(C)=O | ||||||||
| InChI Identifier | InChI=1S/C8H15NO6/c1-3(11)9-8-7(14)6(13)5(12)4(2-10)15-8/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6+,7-,8-/m1/s1 | ||||||||
| InChI Key | IBONACLSSOLHFU-JAJWTYFOSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
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| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
