Showing metabocard for N-Lauroyl-L-Lysine (MMDBc0061027)
Microbial
Human
Record Information | |||||||||||||
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Version | 1.0 | ||||||||||||
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 | ||||||||||||
Alternative Parents | |||||||||||||
Substituents |
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Molecular Framework | Aliphatic acyclic compounds | ||||||||||||
External Descriptors | Not Available | ||||||||||||
Functional Ontology | |||||||||||||
Not Available | |||||||||||||
Physical Properties | |||||||||||||
State | Not Available | ||||||||||||
Predicted Properties | Not Available | ||||||||||||
Spectra | |||||||||||||
Not Available | |||||||||||||
Biological Properties | |||||||||||||
Cellular Locations | Not Available | ||||||||||||
Biospecimen Locations | Not Available | ||||||||||||
Tissue Locations | Not Available | ||||||||||||
Associated OMIM IDs | |||||||||||||
Human Proteins and Enzymes | |||||||||||||
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Human Pathways | |||||||||||||
Pathways |
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Microbial Pathways | |||||||||||||
Pathways | This table shows at most 5 pathways. For the full list of associated pathways: See All Associated Bacterial Pathways
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Metabolic Reactions | |||||||||||||
Reactions This table shows at most 20 reactions. For the full list of associated reactions: See All Associated Reactions
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Health Effects and Bioactivity | |||||||||||||
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Microbial Sources | |||||||||||||
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Exposure Sources | |||||||||||||
Other Exposures |
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Host Biospecimen and Location | |||||||||||||
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External Links | |||||||||||||
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 | ||||||||||||
References | |||||||||||||
Synthesis Reference | Not Available | ||||||||||||
General References |
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