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Details

Stereochemistry ACHIRAL
Molecular Formula C18H34O2.C4H11NO2
Molecular Weight 387.597
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of DIETHANOLAMINE OLEATE

SMILES

OCCNCCO.CCCCCCCC\C=C/CCCCCCCC(O)=O

InChI

InChIKey=KQHZEKNQJJSVDN-KVVVOXFISA-N
InChI=1S/C18H34O2.C4H11NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;6-3-1-5-2-4-7/h9-10H,2-8,11-17H2,1H3,(H,19,20);5-7H,1-4H2/b10-9-;

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including https://www.google.com/patents/CN106391143A | https://www.ncbi.nlm.nih.gov/pubmed/6387722 | https://www.ncbi.nlm.nih.gov/pubmed/18281954 | https://www.ncbi.nlm.nih.gov/pubmed/18281954

Diethanolamine oleate is clear golden-brown viscous liquid, that used as a surfactant and a corrosion inhibitor. Diethanolamine oleate prolonged mean survival time of mice with Ehrlich exudative carcinoma. The increase in mean survival time after administration of diethanolamine oleate was 8.3%.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Cytotoxic action of diethanolamine oleate on Ehrlich exudative carcinoma in mice, compared with the action of polyoxyethylene sorbitan mono-oleate (Tween 80).
1979
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Oral
Human embryonic kidney cells (HEK293), human hepatocellular carcinoma cells (HepG2), human neuroblastoma cells (SH-SY5Y and SK-N-SH), human leukemia T cells (Jurkat, clone E6-1), normal human foreskin fibroblasts (BJ) from a single donor (newborn male), normal human lung fibroblasts (MRC-5) from a single donor (male; 14 weeks gestation), normal human vascular endothelial cells (HUV-EC-C), rat hepatoma cells (H4-II-E), mouse neuroblastoma cells (N2a), and mouse fibroblast cells (NIH 3T3) were used for activity evaluation. After the cells were dispensed into 1536-well plates and incubated for 5–6 h, 23 nL of Diethanolamine oleate was transferred into the wells using a pin tool, resulting in final concentrations of 0.5 nM to 46 µM of Diethanolamine oleate and 0.45% DMSO. To achieve the highest final Diethanolamine oleate concentration of 92 µM (DMSO concentration 0.9%), 23 nL of Diethanolamine oleate was transferred twice from the highest concentration mother plate into each well of the assay plate; control plates using DMSO only at this highest concentration were also included. Caspase-3/7 activity was measured using a homogeneous luminescent method.
Name Type Language
DIETHANOLAMINE OLEATE
Systematic Name English
OLEIC ACID DIETHANOLAMINE SALT
Preferred Name English
OLEIC ACID, DIETHANOLAMINE SALT
Common Name English
Code System Code Type Description
CAS
13961-86-9
Created by admin on Mon Mar 31 21:46:33 GMT 2025 , Edited by admin on Mon Mar 31 21:46:33 GMT 2025
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PUBCHEM
6433588
Created by admin on Mon Mar 31 21:46:33 GMT 2025 , Edited by admin on Mon Mar 31 21:46:33 GMT 2025
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ECHA (EC/EINECS)
237-740-0
Created by admin on Mon Mar 31 21:46:33 GMT 2025 , Edited by admin on Mon Mar 31 21:46:33 GMT 2025
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HSDB
4190
Created by admin on Mon Mar 31 21:46:33 GMT 2025 , Edited by admin on Mon Mar 31 21:46:33 GMT 2025
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FDA UNII
RF675SKV94
Created by admin on Mon Mar 31 21:46:33 GMT 2025 , Edited by admin on Mon Mar 31 21:46:33 GMT 2025
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EPA CompTox
DTXSID9023831
Created by admin on Mon Mar 31 21:46:33 GMT 2025 , Edited by admin on Mon Mar 31 21:46:33 GMT 2025
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