3-Nitrophenyl alpha-D-galactopyranoside (CHEM101210)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-05 12:12:19 UTC | ||||||||
| Update Date | 2026-08-18 18:32:13 UTC | ||||||||
| Accession Number | CHEM101210 | ||||||||
| Identification | |||||||||
| Common Name | 3-Nitrophenyl alpha-D-galactopyranoside | ||||||||
| Class | Small Molecule | ||||||||
| Description | 3-Nitrophenyl alpha-D-galactopyranoside belongs to the carbohydrates and carbohydrate conjugates, a subclass of organooxygen compounds within the organic compounds. This compound has the formula C12H15NO8 and an average molecular weight of 301.25 g/mol. It is recorded to have two protein targets: the Cholera enterotoxin subunit B (ctxB) and the Heat-labile enterotoxin B chain (eltB). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C12H15NO8 | ||||||||
| Average Molecular Mass | 301.251 g/mol | ||||||||
| Monoisotopic Mass | 301.080 g/mol | ||||||||
| CAS Registry Number | 52571-71-8 | ||||||||
| IUPAC Name | (2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-(3-nitrophenoxy)oxane-3,4,5-triol | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | OC[C@H]1O[C@H](OC2=CC=CC(=C2)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@H]1O | ||||||||
| InChI Identifier | InChI=1S/C12H15NO8/c14-5-8-9(15)10(16)11(17)12(21-8)20-7-3-1-2-6(4-7)13(18)19/h1-4,8-12,14-17H,5H2/t8-,9+,10+,11-,12+/m1/s1 | ||||||||
| InChI Key | VCCMGHVCRFMITI-IIRVCBMXSA-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 | ||||||||
