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
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+
| 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
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2782 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15261286 |
63.0 nM [IC50] | ||
Target ID: CHEMBL2243 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16078824 |
68.0 nM [IC50] |
PubMed
| Title | Date | PubMed |
|---|---|---|
| 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
Edited
Mon Mar 31 21:55:25 GMT 2025
by
admin
on
Mon Mar 31 21:55:25 GMT 2025
|
| Record UNII |
GOU8K597IT
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 |