| Record Information |
|---|
| Version | 1.0 |
|---|
| Creation Date | 2018-06-25 21:50:54 UTC |
|---|
| Update Date | 2020-03-13 17:33:41 UTC |
|---|
| BMDB ID | BMDB0062103 |
|---|
| Secondary Accession Numbers | |
|---|
| Metabolite Identification |
|---|
| Common Name | N-acetyl-Muramic acid |
|---|
| Description | N-Acetylmuramate, also known as acetylmuramic acid or 4-O-nacmur, belongs to the class of organic compounds known as acylaminosugars. These are organic compounds containing a sugar linked to a chain through N-acyl group. N-Acetylmuramate is possibly soluble (in water) and a moderately basic compound (based on its pKa). N-Acetylmuramate exists in all living organisms, ranging from bacteria to humans. |
|---|
| Structure | |
|---|
| Synonyms | | Value | Source |
|---|
| N-Acetyl-D-muramoate | ChEBI | | N-Acetylmuramic acid | ChEBI | | N-Acetyl-D-muramoic acid | Generator | | N-Acetylisomuramic acid | HMDB | | Acetylmuramic acid | HMDB | | 2-Acetamido-4-O-(1-carboxyethyl)-2-deoxyglucose | HMDB | | 2-Acetamido-3-O-((S)-1-carboxyethyl)-2-deoxy-D-glucose | HMDB | | 2-Acetamido-4-O-(1-carboxyethyl)-2-deoxyglucose, (beta-D)-isomer | HMDB | | 4-O-NAcMur | HMDB | | N-Acetylmuramate | Generator | | N-Acetyl-D-muramate | Generator |
|
|---|
| Chemical Formula | C11H19NO8 |
|---|
| Average Molecular Weight | 293.2705 |
|---|
| Monoisotopic Molecular Weight | 293.111066589 |
|---|
| IUPAC Name | (2R)-2-{[(3R,4R,5S,6R)-2,5-dihydroxy-3-[(1-hydroxyethylidene)amino]-6-(hydroxymethyl)oxan-4-yl]oxy}propanoic acid |
|---|
| Traditional Name | (2R)-2-{[(3R,4R,5S,6R)-2,5-dihydroxy-3-[(1-hydroxyethylidene)amino]-6-(hydroxymethyl)oxan-4-yl]oxy}propanoic acid |
|---|
| CAS Registry Number | 61633-75-8 |
|---|
| SMILES | [H][C@](C)(O[C@@]1([H])[C@]([H])(O)[C@@]([H])(CO)OC([H])(O)[C@]1([H])N=C(C)O)C(O)=O |
|---|
| InChI Identifier | InChI=1S/C11H19NO8/c1-4(10(16)17)19-9-7(12-5(2)14)11(18)20-6(3-13)8(9)15/h4,6-9,11,13,15,18H,3H2,1-2H3,(H,12,14)(H,16,17)/t4-,6-,7-,8-,9-,11?/m1/s1 |
|---|
| InChI Key | MNLRQHMNZILYPY-MKFCKLDKSA-N |
|---|
| Chemical Taxonomy |
|---|
| Description | belongs to the class of organic compounds known as acylaminosugars. These are organic compounds containing a sugar linked to a chain through N-acyl group. |
|---|
| Kingdom | Organic compounds |
|---|
| Super Class | Organic oxygen compounds |
|---|
| Class | Organooxygen compounds |
|---|
| Sub Class | Carbohydrates and carbohydrate conjugates |
|---|
| Direct Parent | Acylaminosugars |
|---|
| Alternative Parents | |
|---|
| Substituents | - Acylaminosugar
- Muramic_acid
- N-acyl-alpha-hexosamine
- Hexose monosaccharide
- Sugar acid
- Monosaccharide
- Oxane
- Acetamide
- Carboxamide group
- Hemiacetal
- Secondary carboxylic acid amide
- Secondary alcohol
- Carboxylic acid derivative
- Carboxylic acid
- Dialkyl ether
- Ether
- Monocarboxylic acid or derivatives
- Oxacycle
- Organoheterocyclic compound
- Carbonyl group
- Organic oxide
- Hydrocarbon derivative
- Organopnictogen compound
- Organic nitrogen compound
- Alcohol
- Organonitrogen compound
- Primary alcohol
- Aliphatic heteromonocyclic compound
|
|---|
| Molecular Framework | Aliphatic heteromonocyclic compounds |
|---|
| External Descriptors | |
|---|
| Ontology |
|---|
| Status | Detected but not Quantified |
|---|
| Origin | Not Available |
|---|
| Biofunction | Not Available |
|---|
| Application | Not Available |
|---|
| Cellular locations | Not Available |
|---|
| Physical Properties |
|---|
| State | Not Available |
|---|
| Experimental Properties | | Property | Value | Reference |
|---|
| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | LogP | Not Available | Not Available |
|
|---|
| Predicted Properties | |
|---|
| Spectra |
|---|
| Spectra | |
|---|