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Details

Stereochemistry ACHIRAL
Molecular Formula C18H35NO
Molecular Weight 281.4766
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ELAIDAMIDE

SMILES

CCCCCCCC\C=C\CCCCCCCC(N)=O

InChI

InChIKey=FATBGEAMYMYZAF-MDZDMXLPSA-N
InChI=1S/C18H35NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-8,11-17H2,1H3,(H2,19,20)/b10-9+

HIDE SMILES / InChI

Molecular Formula C18H35NO
Molecular Weight 281.4766
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
63.0 nM [IC50]
68.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Role of heteromeric gap junctions in the cytotoxicity of cisplatin.
2013-08-09
A second fatty acid amide hydrolase with variable distribution among placental mammals.
2006-12-01
Gap junction communications influence upon fibroblast synthesis of Type I collagen and fibronectin.
2006-07-01
Selective effect of oleamide, an endogenous sleep-inducing lipid amide, on pentylenetetrazole-induced seizures in mice.
2003-08
Effects of oleamide on choline acetyltransferase and cognitive activities.
2003-06
Deletion of the GABA(A) receptor beta 3 subunit eliminates the hypnotic actions of oleamide in mice.
2001-12-21
Allosteric regulation by oleamide of the binding properties of 5-hydroxytryptamine7 receptors.
1999-12-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:55:25 GMT 2025
Edited
by admin
on Mon Mar 31 21:55:25 GMT 2025
Record UNII
GOU8K597IT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ELAIDAMIDE
Systematic Name English
(E)-9,10-OCTADECENAMIDE
Preferred Name English
ELAIDOYLAMIDE
Systematic Name English
TRANS-9-OCTADECENAMIDE
Systematic Name English
ELAIDIC ACID AMIDE
Systematic Name English
9-OCTADECENAMIDE, (9E)-
Systematic Name English
Code System Code Type Description
CAS
4303-70-2
Created by admin on Mon Mar 31 21:55:25 GMT 2025 , Edited by admin on Mon Mar 31 21:55:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID901017170
Created by admin on Mon Mar 31 21:55:25 GMT 2025 , Edited by admin on Mon Mar 31 21:55:25 GMT 2025
PRIMARY
DRUG BANK
DB03784
Created by admin on Mon Mar 31 21:55:25 GMT 2025 , Edited by admin on Mon Mar 31 21:55:25 GMT 2025
PRIMARY
CAS
3322-62-1
Created by admin on Mon Mar 31 21:55:25 GMT 2025 , Edited by admin on Mon Mar 31 21:55:25 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
ECHA (EC/EINECS)
224-316-5
Created by admin on Mon Mar 31 21:55:25 GMT 2025 , Edited by admin on Mon Mar 31 21:55:25 GMT 2025
PRIMARY
PUBCHEM
5353370
Created by admin on Mon Mar 31 21:55:25 GMT 2025 , Edited by admin on Mon Mar 31 21:55:25 GMT 2025
PRIMARY
FDA UNII
GOU8K597IT
Created by admin on Mon Mar 31 21:55:25 GMT 2025 , Edited by admin on Mon Mar 31 21:55:25 GMT 2025
PRIMARY