2-Acetamido-2-Deoxy-D-Glucono-1,5-Lactone (CHEM100932)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-05 12:02:03 UTC | ||||||||
| Update Date | 2026-05-14 17:46:30 UTC | ||||||||
| Accession Number | CHEM100932 | ||||||||
| Identification | |||||||||
| Common Name | 2-Acetamido-2-Deoxy-D-Glucono-1,5-Lactone | ||||||||
| Class | Small Molecule | ||||||||
| Description | 2-Acetamido-2-Deoxy-D-Glucono-1,5-Lactone is an organic compound with the formula C8H13NO6 and an average molecular weight of 219.19 g/mol. 2-Acetamido-2-Deoxy-D-Glucono-1,5-Lactone belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. This compound is associated with two recorded protein targets: Chitinase B (chiB) and Beta-hexosaminidase subunit beta (HEXB). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C8H13NO6 | ||||||||
| Average Molecular Mass | 219.192 g/mol | ||||||||
| Monoisotopic Mass | 219.074 g/mol | ||||||||
| CAS Registry Number | 19026-22-3 | ||||||||
| IUPAC Name | N-[(3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-oxooxan-3-yl]acetamide | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1=O | ||||||||
| InChI Identifier | InChI=1S/C8H13NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-7,10,12-13H,2H2,1H3,(H,9,11)/t4-,5-,6-,7-/m1/s1 | ||||||||
| InChI Key | NELQYZRSPDCGRQ-DBRKOABJSA-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 | ||||||||
| Spectra | |||||||||
| Spectra |
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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 | |||||||||
| Not Available | |||||||||
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| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
