Basic Info

Common NameEthanolamine(F05504)
2D Structure
Description

Ethanolamine is a viscous, hygroscopic amino alcohol with an ammoniacal odor. It is widely distributed in biological tissue and is a component of lecithin. It is used as a surfactant, fluorometric reagent, and to remove CO2 and H2S from natural gas and other gases.

FRCD IDF05504
CAS Number141-43-5
PubChem CID700
FormulaC2H7NO
IUPAC Name

2-aminoethanol

InChI Key

HZAXFHJVJLSVMW-UHFFFAOYSA-N

InChI

InChI=1S/C2H7NO/c3-1-2-4/h4H,1-3H2

Canonical SMILES

C(CO)N

Isomeric SMILES

C(CO)N

WikipediaEthanolamine
Synonyms
        
            2-Amino-1-ethanol
        
            Ethanolamine
        
            2-aminoethanol
        
            monoethanolamine
        
            141-43-5
        
            Aminoethanol
        
            2-Hydroxyethylamine
        
            colamine
        
            Glycinol
        
            Olamine
        
Classifies
                

                  
                    Animal Toxin
                  

                
        
Update DateNov 13, 2018 17:07

Chemical Taxonomy

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClassOrganonitrogen compounds
SubclassAmines
Intermediate Tree NodesAlkanolamines
Direct Parent1,2-aminoalcohols
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
Substituents1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom.

Properties

Property NameProperty Value
Molecular Weight61.084
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Complexity10
Monoisotopic Mass61.053
Exact Mass61.053
XLogP-1.3
Formal Charge0
Heavy Atom Count4
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

ADMET

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.5519
Human Intestinal AbsorptionHIA+0.8172
Caco-2 PermeabilityCaco2+0.5655
P-glycoprotein SubstrateNon-substrate0.6655
P-glycoprotein InhibitorNon-inhibitor0.9748
Non-inhibitor0.9673
Renal Organic Cation TransporterNon-inhibitor0.8250
Distribution
Subcellular localizationLysosome0.9101
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8833
CYP450 2D6 SubstrateNon-substrate0.7326
CYP450 3A4 SubstrateNon-substrate0.8369
CYP450 1A2 InhibitorNon-inhibitor0.9027
CYP450 2C9 InhibitorNon-inhibitor0.9470
CYP450 2D6 InhibitorNon-inhibitor0.9700
CYP450 2C19 InhibitorNon-inhibitor0.9572
CYP450 3A4 InhibitorNon-inhibitor0.8944
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9477
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.7631
Non-inhibitor0.8950
AMES ToxicityNon AMES toxic0.9030
CarcinogensNon-carcinogens0.6357
Fish ToxicityLow FHMT0.9517
Tetrahymena Pyriformis ToxicityLow TPT1.0000
Honey Bee ToxicityLow HBT0.5726
BiodegradationReady biodegradable0.7562
Acute Oral ToxicityIII0.8057
Carcinogenicity (Three-class)Non-required0.6707

Model Value Unit
Absorption
Aqueous solubility0.7514LogS
Caco-2 Permeability0.6875LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.5185LD50, mol/kg
Fish Toxicity3.1908pLC50, mg/L
Tetrahymena Pyriformis Toxicity-1.5151pIGC50, ug/L

References

TitleJournalDatePubmed ID
Sensitivity enhancement for mycotoxin determination by optical waveguide lightmode spectroscopy using gold nanoparticles of different size and origin.Food Chem2018 Nov 3029934142
Ethanolamine utilization supports Clostridium perfringens growth in infected tissues.Microb Pathog2018 Jun29654901
Docosahexaenoic acid attenuates in endocannabinoid synthesis in RAW 264.7 macrophages activated with benzo(a)pyrene and lipopolysaccharide.Toxicol Lett2016 Sep 627329536
Highly sensitive detection of lipopolysaccharides using an aptasensor based on hybridization chain reaction.Sci Rep2016 Jul 1227404735
Waste grape skins: evaluation of safety aspects for the production of functional powders and extracts for the food sector.Food Addit Contam Part A Chem Anal Control Expo Risk Assess2016 Jul27295010
MS/MS and LC-MS/MS analysis of choline/ethanolamine plasmalogens via promotion ofalkali metal adduct formation.J Chromatogr B Analyt Technol Biomed Life Sci2015 Nov 126447938
Transcriptional and Post Transcriptional Control of Enterococcal Gene Regulation201424649509
[EHEC carriage in ruminants and probiotic effects].Biol Aujourdhui201324594574
A metabolomics approach to uncover the effects of grain diets on rumen health in dairy cows.J Dairy Sci2012 Nov22959937
Free amino acids and biogenic amines in Alicante Monastrell wines.Food Chem2012 Dec 122953887
Comparative genomic hybridization analysis shows different epidemiology of chromosomal and plasmid-borne cpe-carrying Clostridium perfringens type A.PLoS One201223094024
[Rapid detection of Escherichia coli O157 : H7 using surface plasmon resonance(SPR) biosensor].Guang Pu Xue Yu Guang Pu Fen Xi2011 Oct22250516
A fast, inexpensive, and safe method for residue analysis of meptyldinocap indifferent fruits by liquid chromatography/tandem mass spectrometry.J AOAC Int2010 Nov-Dec21313826
The role of plasmalogen in the oxidative stability of neutral lipids andphospholipids.J Agric Food Chem2010 Feb 2420099826
Global regulation of food supply by Pseudomonas putida DOT-T1E.J Bacteriol2010 Apr20139187
Delivery of interleukin-18 gene to lung cancer cells using cationic emulsion.J Drug Target2009 Jan19016067
Regulation of the Saccharomyces cerevisiae EKI1-encoded ethanolamine kinase byzinc depletion.J Biol Chem2006 May 1216551612
Spectrophotometric total protein assay with copper(II)-neocuproine reagent inalkaline medium.Talanta2006 Feb 2818970504
Growth inhibition of Listeria monocytogenes by a nonbacteriocinogenicCarnobacterium piscicola.J Appl Microbiol200515610430
Oleoylethanolamide stimulates lipolysis by activating the nuclear receptorperoxisome proliferator-activated receptor alpha (PPAR-alpha).J Biol Chem2004 Jul 215123613

Targets

General Function:
Zinc ion binding
Specific Function:
Nuclear receptor that binds DNA as a monomer to ROR response elements (RORE) containing a single core motif half-site 5'-AGGTCA-3' preceded by a short A-T-rich sequence. Key regulator of cellular differentiation, immunity, peripheral circadian rhythm as well as lipid, steroid, xenobiotics and glucose metabolism. Considered to have intrinsic transcriptional activity, have some natural ligands like oxysterols that act as agonists (25-hydroxycholesterol) or inverse agonists (7-oxygenated sterols), enhancing or repressing the transcriptional activity, respectively. Recruits distinct combinations of cofactors to target gene regulatory regions to modulate their transcriptional expression, depending on the tissue, time and promoter contexts. Regulates the circadian expression of clock genes such as CRY1, ARNTL/BMAL1 and NR1D1 in peripheral tissues and in a tissue-selective manner. Competes with NR1D1 for binding to their shared DNA response element on some clock genes such as ARNTL/BMAL1, CRY1 and NR1D1 itself, resulting in NR1D1-mediated repression or RORC-mediated activation of the expression, leading to the circadian pattern of clock genes expression. Therefore influences the period length and stability of the clock. Involved in the regulation of the rhythmic expression of genes involved in glucose and lipid metabolism, including PLIN2 and AVPR1A. Negative regulator of adipocyte differentiation through the regulation of early phase genes expression, such as MMP3. Controls adipogenesis as well as adipocyte size and modulates insulin sensitivity in obesity. In liver, has specific and redundant functions with RORA as positive or negative modulator of expression of genes encoding phase I and Phase II proteins involved in the metabolism of lipids, steroids and xenobiotics, such as SULT1E1. Also plays also a role in the regulation of hepatocyte glucose metabolism through the regulation of G6PC and PCK1. Regulates the rhythmic expression of PROX1 and promotes its nuclear localization (By similarity). Plays an indispensable role in the induction of IFN-gamma dependent anti-mycobacterial systemic immunity (PubMed:26160376).Isoform 2: Essential for thymopoiesis and the development of several secondary lymphoid tissues, including lymph nodes and Peyer's patches. Required for the generation of LTi (lymphoid tissue inducer) cells. Regulates thymocyte survival through DNA-binding on ROREs of target gene promoter regions and recruitment of coactivaros via the AF-2. Also plays a key role, downstream of IL6 and TGFB and synergistically with RORA, for lineage specification of uncommitted CD4(+) T-helper (T(H)) cells into T(H)17 cells, antagonizing the T(H)1 program. Probably regulates IL17 and IL17F expression on T(H) by binding to the essential enhancer conserved non-coding sequence 2 (CNS2) in the IL17-IL17F locus. May also play a role in the pre-TCR activation cascade leading to the maturation of alpha/beta T-cells and may participate in the regulation of DNA accessibility in the TCR-J(alpha) locus.
Gene Name:
RORC
Uniprot ID:
P51449
Molecular Weight:
58194.845 Da
References
  1. Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
General Function:
Phospholipase a2 inhibitor activity
Specific Function:
Inhibitor of phospholipase A2, also possesses anti-coagulant properties. Also cleaves the cyclic bond of inositol 1,2-cyclic phosphate to form inositol 1-phosphate.
Gene Name:
ANXA3
Uniprot ID:
P12429
Molecular Weight:
36374.85 Da
General Function:
Zinc ion binding
Specific Function:
NAD-dependent protein deacetylase, which deacetylates internal lysines on histone and alpha-tubulin as well as many other proteins such as key transcription factors. Participates in the modulation of multiple and diverse biological processes such as cell cycle control, genomic integrity, microtubule dynamics, cell differentiation, metabolic networks, and autophagy. Plays a major role in the control of cell cycle progression and genomic stability. Functions in the antephase checkpoint preventing precocious mitotic entry in response to microtubule stress agents, and hence allowing proper inheritance of chromosomes. Positively regulates the anaphase promoting complex/cyclosome (APC/C) ubiquitin ligase complex activity by deacetylating CDC20 and FZR1, then allowing progression through mitosis. Associates both with chromatin at transcriptional start sites (TSSs) and enhancers of active genes. Plays a role in cell cycle and chromatin compaction through epigenetic modulation of the regulation of histone H4 'Lys-20' methylation (H4K20me1) during early mitosis. Specifically deacetylates histone H4 at 'Lys-16' (H4K16ac) between the G2/M transition and metaphase enabling H4K20me1 deposition by SETD8 leading to ulterior levels of H4K20me2 and H4K20me3 deposition throughout cell cycle, and mitotic S-phase progression. Deacetylates SETD8 modulating SETD8 chromatin localization during the mitotic stress response. Deacetylates also histone H3 at 'Lys-57' (H3K56ac) during the mitotic G2/M transition. Upon bacterium Listeria monocytogenes infection, deacetylates 'Lys-18' of histone H3 in a receptor tyrosine kinase MET- and PI3K/Akt-dependent manner, thereby inhibiting transcriptional activity and promoting late stages of listeria infection. During oocyte meiosis progression, may deacetylate histone H4 at 'Lys-16' (H4K16ac) and alpha-tubulin, regulating spindle assembly and chromosome alignment by influencing microtubule dynamics and kinetochore function. Deacetylates alpha-tubulin at 'Lys-40' and hence controls neuronal motility, oligodendroglial cell arbor projection processes and proliferation of non-neuronal cells. Phosphorylation at Ser-368 by a G1/S-specific cyclin E-CDK2 complex inactivates SIRT2-mediated alpha-tubulin deacetylation, negatively regulating cell adhesion, cell migration and neurite outgrowth during neuronal differentiation. Deacetylates PARD3 and participates in the regulation of Schwann cell peripheral myelination formation during early postnatal development and during postinjury remyelination. Involved in several cellular metabolic pathways. Plays a role in the regulation of blood glucose homeostasis by deacetylating and stabilizing phosphoenolpyruvate carboxykinase PCK1 activity in response to low nutrient availability. Acts as a key regulator in the pentose phosphate pathway (PPP) by deacetylating and activating the glucose-6-phosphate G6PD enzyme, and therefore, stimulates the production of cytosolic NADPH to counteract oxidative damage. Maintains energy homeostasis in response to nutrient deprivation as well as energy expenditure by inhibiting adipogenesis and promoting lipolysis. Attenuates adipocyte differentiation by deacetylating and promoting FOXO1 interaction to PPARG and subsequent repression of PPARG-dependent transcriptional activity. Plays a role in the regulation of lysosome-mediated degradation of protein aggregates by autophagy in neuronal cells. Deacetylates FOXO1 in response to oxidative stress or serum deprivation, thereby negatively regulating FOXO1-mediated autophagy. Deacetylates a broad range of transcription factors and co-regulators regulating target gene expression. Deacetylates transcriptional factor FOXO3 stimulating the ubiquitin ligase SCF(SKP2)-mediated FOXO3 ubiquitination and degradation. Deacetylates HIF1A and therefore promotes HIF1A degradation and inhibition of HIF1A transcriptional activity in tumor cells in response to hypoxia. Deacetylates RELA in the cytoplasm inhibiting NF-kappaB-dependent transcription activation upon TNF-alpha stimulation. Inhibits transcriptional activation by deacetylating p53/TP53 and EP300. Deacetylates also EIF5A. Functions as a negative regulator on oxidative stress-tolerance in response to anoxia-reoxygenation conditions. Plays a role as tumor suppressor.Isoform 1: Deacetylates EP300, alpha-tubulin and histone H3 and H4.Isoform 2: Deacetylates EP300, alpha-tubulin and histone H3 and H4.Isoform 5: Lacks deacetylation activity.
Gene Name:
SIRT2
Uniprot ID:
Q8IXJ6
Molecular Weight:
43181.7 Da
References
  1. Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
General Function:
Transcription regulatory region dna binding
Specific Function:
Ligand-activated transcriptional activator. Binds to the XRE promoter region of genes it activates. Activates the expression of multiple phase I and II xenobiotic chemical metabolizing enzyme genes (such as the CYP1A1 gene). Mediates biochemical and toxic effects of halogenated aromatic hydrocarbons. Involved in cell-cycle regulation. Likely to play an important role in the development and maturation of many tissues. Regulates the circadian clock by inhibiting the basal and circadian expression of the core circadian component PER1. Inhibits PER1 by repressing the CLOCK-ARNTL/BMAL1 heterodimer mediated transcriptional activation of PER1.
Gene Name:
AHR
Uniprot ID:
P35869
Molecular Weight:
96146.705 Da
References
  1. Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]