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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

Molecular Formula C18H34O2
Molecular Weight 282.4614
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Molecular Formula C4H11NO2
Molecular Weight 105.1356
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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.
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:56:08 GMT 2023
Edited
by admin
on Sat Dec 16 07:56:08 GMT 2023
Record UNII
RF675SKV94
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIETHANOLAMINE OLEATE
Systematic Name English
OLEIC ACID DIETHANOLAMINE SALT
Common Name English
OLEIC ACID, DIETHANOLAMINE SALT
Common Name English
Code System Code Type Description
CAS
13961-86-9
Created by admin on Sat Dec 16 07:56:08 GMT 2023 , Edited by admin on Sat Dec 16 07:56:08 GMT 2023
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PUBCHEM
6433588
Created by admin on Sat Dec 16 07:56:08 GMT 2023 , Edited by admin on Sat Dec 16 07:56:08 GMT 2023
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ECHA (EC/EINECS)
237-740-0
Created by admin on Sat Dec 16 07:56:08 GMT 2023 , Edited by admin on Sat Dec 16 07:56:08 GMT 2023
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HSDB
4190
Created by admin on Sat Dec 16 07:56:08 GMT 2023 , Edited by admin on Sat Dec 16 07:56:08 GMT 2023
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FDA UNII
RF675SKV94
Created by admin on Sat Dec 16 07:56:08 GMT 2023 , Edited by admin on Sat Dec 16 07:56:08 GMT 2023
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EPA CompTox
DTXSID9023831
Created by admin on Sat Dec 16 07:56:08 GMT 2023 , Edited by admin on Sat Dec 16 07:56:08 GMT 2023
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