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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
Structure of LAUROYL LYSINE

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

HIDE SMILES / InChI

Molecular Formula C18H36N2O3
Molecular Weight 328.49
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
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 Jan 11
Efficient Nepsilon-lauroyl-L-lysine production by recombinant epsilon-lysine acylase from Streptomyces mobaraensis.
2009 May 20
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 20:01:03 UTC 2023
Edited
by admin
on Sat Dec 16 20:01:03 UTC 2023
Record UNII
113171Q70B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LAUROYL LYSINE
INCI  
INCI  
Official Name English
LAUROYLLYSINE
Systematic Name English
LYSINE, N6-LAUROYL-, L-
Systematic Name English
LAUROYL LYSINE [INCI]
Common Name English
CORUM 5105
Brand Name English
L-LYSINE, N6-(1-OXODODECYL)-
Systematic Name English
N-.EPSILON.-LAUROYL-L-LYSINE
Common Name English
ORISTAR LOL
Brand Name English
AMIHOPE LL
Brand Name English
FAMEX L 12
Brand Name English
Code System Code Type Description
PUBCHEM
104151
Created by admin on Sat Dec 16 20:01:03 UTC 2023 , Edited by admin on Sat Dec 16 20:01:03 UTC 2023
PRIMARY
CAS
52315-75-0
Created by admin on Sat Dec 16 20:01:03 UTC 2023 , Edited by admin on Sat Dec 16 20:01:03 UTC 2023
PRIMARY
ECHA (EC/EINECS)
257-843-4
Created by admin on Sat Dec 16 20:01:03 UTC 2023 , Edited by admin on Sat Dec 16 20:01:03 UTC 2023
PRIMARY
DAILYMED
113171Q70B
Created by admin on Sat Dec 16 20:01:03 UTC 2023 , Edited by admin on Sat Dec 16 20:01:03 UTC 2023
PRIMARY
EPA CompTox
DTXSID80885998
Created by admin on Sat Dec 16 20:01:03 UTC 2023 , Edited by admin on Sat Dec 16 20:01:03 UTC 2023
PRIMARY
FDA UNII
113171Q70B
Created by admin on Sat Dec 16 20:01:03 UTC 2023 , Edited by admin on Sat Dec 16 20:01:03 UTC 2023
PRIMARY
RXCUI
1426404
Created by admin on Sat Dec 16 20:01:03 UTC 2023 , Edited by admin on Sat Dec 16 20:01:03 UTC 2023
PRIMARY RxNorm