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
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-;
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 |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/475555Curator'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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/475555
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
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/475555
Unknown
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18281954
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
Edited
Sat Dec 16 07:56:08 GMT 2023
by
admin
on
Sat Dec 16 07:56:08 GMT 2023
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Record UNII |
RF675SKV94
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Record Status |
Validated (UNII)
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Record Version |
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