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Details

Stereochemistry RACEMIC
Molecular Formula C19H37NO4
Molecular Weight 343.5014
Optical Activity ( + / - )
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LAUROYLCARNITINE, (±)-

SMILES

CCCCCCCCCCCC(=O)OC(CC([O-])=O)C[N+](C)(C)C

InChI

InChIKey=FUJLYHJROOYKRA-UHFFFAOYSA-N
InChI=1S/C19H37NO4/c1-5-6-7-8-9-10-11-12-13-14-19(23)24-17(15-18(21)22)16-20(2,3)4/h17H,5-16H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C19H37NO4
Molecular Weight 343.5014
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: O14493
Gene ID: 1364.0
Gene Symbol: CLDN4
Target Organism: Homo sapiens (Human)
Target ID: O00501
Gene ID: 7122.0
Gene Symbol: CLDN5
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Absorption enhancement effect of acylcarnitines through changes in tight junction protein in Caco-2 cell monolayers.
2011
Enhancement of nasal salmon calcitonin absorption by lauroylcarnitine chloride in rats.
1996-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:06:36 GMT 2025
Edited
by admin
on Mon Mar 31 21:06:36 GMT 2025
Record UNII
0NQ3RVU3HG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DL-LAUROYLCARNITINE
Preferred Name English
LAUROYLCARNITINE, (±)-
Systematic Name English
LAUROYL DL-CARNITINE
Common Name English
AMMONIUM, (3-CARBOXY-2-HYDROXYPROPYL)TRIMETHYL-, HYDROXIDE, INNER SALT, LAURATE
Systematic Name English
1-PROPANAMINIUM, 3-CARBOXY-N,N,N-TRIMETHYL-2-((1-OXODODECYL)OXY)-, INNER SALT
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID401316781
Created by admin on Mon Mar 31 21:06:36 GMT 2025 , Edited by admin on Mon Mar 31 21:06:36 GMT 2025
PRIMARY
FDA UNII
0NQ3RVU3HG
Created by admin on Mon Mar 31 21:06:36 GMT 2025 , Edited by admin on Mon Mar 31 21:06:36 GMT 2025
PRIMARY
PUBCHEM
10427569
Created by admin on Mon Mar 31 21:06:36 GMT 2025 , Edited by admin on Mon Mar 31 21:06:36 GMT 2025
PRIMARY
CAS
2466-77-5
Created by admin on Mon Mar 31 21:06:36 GMT 2025 , Edited by admin on Mon Mar 31 21:06:36 GMT 2025
PRIMARY