Showing metabocard for N-Lauroyl-L-Lysine (MMDBc0061027)
Microbial
Human
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| Version | 2.0 | |||||||||||||||
| Status | Detected and Quantified | |||||||||||||||
| Creation Date | 2025-10-03 02:28:58 UTC | |||||||||||||||
| Update Date | 2025-10-08 21:35:40 UTC | |||||||||||||||
| Metabolite ID | MMDBc0061027 | |||||||||||||||
| Metabolite Identification | ||||||||||||||||
| Common Name | N-Lauroyl-L-Lysine | |||||||||||||||
| Description | N-Lauroyl-L-Lysine is a fatty acid derivative of the amino acid L-lysine, classified as an acylated amino acid. Its chemical structure features a lauroyl group (a dodecanoyl chain) linked to the amino group of L-lysine, which imparts amphiphilic properties to the molecule. This unique structure allows N-Lauroyl-L-Lysine to participate in various chemical reactions and pathways, particularly in the synthesis of complex molecular structures. For instance, it has been utilized in the fabrication of triple-functional molecular polyoxometalates (POMs), specifically NLLnH6-nV2Mo18O62 (where n = 1-6), using N-Lauroyl-L-Lysine as a precursor alongside H6V2Mo18O62 (PMID:39622109 ). This highlights its role in the development of advanced materials with potential applications in catalysis and nanotechnology. Additionally, N-Lauroyl-L-Lysine may influence cellular processes due to its interactions with lipid membranes and proteins, although specific biological pathways involving this compound require further investigation. | |||||||||||||||
| Structure |  | |||||||||||||||
| Synonyms | Not Available | |||||||||||||||
| Molecular Formula | C18H36N2O3 | |||||||||||||||
| Average Mass | 328.497 | |||||||||||||||
| Monoisotopic Mass | 328.272593027 | |||||||||||||||
| IUPAC Name | Not Available | |||||||||||||||
| Traditional Name | Not Available | |||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||
| SMILES | Not Available | |||||||||||||||
| InChI Identifier | Not Available | |||||||||||||||
| InChI Key | PDQICKRFOKDJCH-INIZCTEOSA-N | |||||||||||||||
| Chemical Taxonomy | ||||||||||||||||
| Description | Belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. | |||||||||||||||
| Kingdom | Organic compounds | |||||||||||||||
| Super Class | Organic acids and derivatives | |||||||||||||||
| Class | Carboxylic acids and derivatives | |||||||||||||||
| Sub Class | Amino acids, peptides, and analogues | |||||||||||||||
| Direct Parent | N-acyl-L-alpha-amino acids | |||||||||||||||
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| Substituents |
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| Molecular Framework | Aliphatic acyclic compounds | |||||||||||||||
| External Descriptors | Not Available | |||||||||||||||
| Functional Ontology | ||||||||||||||||
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| Physical Properties | ||||||||||||||||
| State | Not Available | |||||||||||||||
| Predicted Properties | Not Available | |||||||||||||||
| Spectra | ||||||||||||||||
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| Chromatographic Retention Times and Retention Indices | ||||||||||||||||
| Retention Times | Not Available | |||||||||||||||
| Retention Indices | Not Available | |||||||||||||||
| Biological Properties | ||||||||||||||||
| Cellular Locations | Not Available | |||||||||||||||
| Biospecimen Locations | Not Available | |||||||||||||||
| Tissue Locations | Not Available | |||||||||||||||
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| Pathways |
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| Pathways | Not Available | |||||||||||||||
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Reactions This table shows at most 20 reactions. For the full list of associated reactions: See All Associated Reactions
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| HMDB ID | Not Available | |||||||||||||||
| DrugBank ID | Not Available | |||||||||||||||
| Phenol Explorer Compound ID | Not Available | |||||||||||||||
| FooDB ID | Not Available | |||||||||||||||
| KNApSAcK ID | Not Available | |||||||||||||||
| Chemspider ID | Not Available | |||||||||||||||
| KEGG Compound ID | Not Available | |||||||||||||||
| BioCyc ID | Not Available | |||||||||||||||
| BiGG ID | Not Available | |||||||||||||||
| Wikipedia Link | Not Available | |||||||||||||||
| METLIN ID | Not Available | |||||||||||||||
| PubChem Compound | 9927445 | |||||||||||||||
| PDB ID | Not Available | |||||||||||||||
| ChEBI ID | Not Available | |||||||||||||||
| Food Biomarker Ontology | Not Available | |||||||||||||||
| CMMC Knowledgebase | PDQICKRFOKDJCH-INIZCTEOSA-N | |||||||||||||||
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