Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C18H36N2O3 |
| Molecular Weight | 328.49 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCC(=O)NCCCC[C@H](N)C(O)=O
InChI
InChIKey=GYDYJUYZBRGMCC-INIZCTEOSA-N
InChI=1S/C18H36N2O3/c1-2-3-4-5-6-7-8-9-10-14-17(21)20-15-12-11-13-16(19)18(22)23/h16H,2-15,19H2,1H3,(H,20,21)(H,22,23)/t16-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Efficient Nepsilon-lauroyl-L-lysine production by recombinant epsilon-lysine acylase from Streptomyces mobaraensis. | 2009-05-20 |
|
| A novel acylase from Streptomyces mobaraensis that efficiently catalyzes hydrolysis/synthesis of capsaicins as well as N-acyl-L-amino acids and N-acyl-peptides. | 2006-01-11 |
Patents
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| Code System | Code | Type | Description | ||
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104151
Created by
admin on Wed Apr 02 18:02:12 GMT 2025 , Edited by admin on Wed Apr 02 18:02:12 GMT 2025
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52315-75-0
Created by
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257-843-4
Created by
admin on Wed Apr 02 18:02:12 GMT 2025 , Edited by admin on Wed Apr 02 18:02:12 GMT 2025
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113171Q70B
Created by
admin on Wed Apr 02 18:02:12 GMT 2025 , Edited by admin on Wed Apr 02 18:02:12 GMT 2025
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DTXSID80885998
Created by
admin on Wed Apr 02 18:02:12 GMT 2025 , Edited by admin on Wed Apr 02 18:02:12 GMT 2025
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113171Q70B
Created by
admin on Wed Apr 02 18:02:12 GMT 2025 , Edited by admin on Wed Apr 02 18:02:12 GMT 2025
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1426404
Created by
admin on Wed Apr 02 18:02:12 GMT 2025 , Edited by admin on Wed Apr 02 18:02:12 GMT 2025
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PRIMARY | RxNorm |
SUBSTANCE RECORD