General Information

MaintermDIETHANOLAMINE
CAS Reg.No.(or other ID)111-42-2
Regnum 175.105
177.2800
176.170
176.180
177.1200
177.2600
176.210

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID8113
IUPAC Name2-(2-hydroxyethylamino)ethanol
InChIInChI=1S/C4H11NO2/c6-3-1-5-2-4-7/h5-7H,1-4H2
InChI KeyZBCBWPMODOFKDW-UHFFFAOYSA-N
Canonical SMILESC(CO)NCCO
Molecular FormulaC4H11NO2
Wikipediadiethanolamine

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight105.137
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Complexity28.9
CACTVS Substructure Key Fingerprint A A A D c c B i M A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A H g A Q C A A A A A D h g A Y A A A L A A g A A A A A A A A A A A A A A A A A A A I A I A A A C E A A A A A A A A A A A E A C Q A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = =
Topological Polar Surface Area52.5
Monoisotopic Mass105.079
Exact Mass105.079
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count7
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


Food Additives Biosynthesis/Degradation


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB-0.5676
Human Intestinal AbsorptionHIA+0.8838
Caco-2 PermeabilityCaco2-0.5263
P-glycoprotein SubstrateNon-substrate0.5248
P-glycoprotein InhibitorNon-inhibitor0.9441
Non-inhibitor0.8358
Renal Organic Cation TransporterNon-inhibitor0.7828
Distribution
Subcellular localizationLysosome0.7743
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8449
CYP450 2D6 SubstrateNon-substrate0.7818
CYP450 3A4 SubstrateNon-substrate0.7991
CYP450 1A2 InhibitorNon-inhibitor0.8633
CYP450 2C9 InhibitorNon-inhibitor0.9512
CYP450 2D6 InhibitorNon-inhibitor0.9541
CYP450 2C19 InhibitorNon-inhibitor0.9384
CYP450 3A4 InhibitorNon-inhibitor0.9615
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9690
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionStrong inhibitor0.6313
Non-inhibitor0.8393
AMES ToxicityNon AMES toxic0.9132
CarcinogensNon-carcinogens0.7699
Fish ToxicityLow FHMT0.8507
Tetrahymena Pyriformis ToxicityLow TPT0.9838
Honey Bee ToxicityLow HBT0.5952
BiodegradationReady biodegradable0.7563
Acute Oral ToxicityIII0.8481
Carcinogenicity (Three-class)Non-required0.7333

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility0.0938LogS
Caco-2 Permeability0.7853LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.8845LD50, mol/kg
Fish Toxicity3.5479pLC50, mg/L
Tetrahymena Pyriformis Toxicity-1.9153pIGC50, ug/L

From admetSAR


Toxicity Profile

Route of Exposure
Mechanism of Toxicity
Metabolism
Toxicity Values
Lethal Dose
Carcinogenicity (IARC Classification)2B, possibly carcinogenic to humans.
Minimum Risk Level
Health Effects
Treatment
Reference
  1. NTP Toxicology and Carcinogenesis Studies of Lauric Acid Diethanolamine Condensate (CAS NO. 120-40-1) in F344/N Rats and B6C3F1 Mice (Dermal Studies). Natl Toxicol Program Tech Rep Ser. 1999 Jul;480:1-200.[12571683 ]
  2. Mathews JM, deCosta K, Thomas BF: Lauramide diethanolamine absorption, metabolism, and disposition in rats and mice after oral, intravenous, and dermal administration. Drug Metab Dispos. 1996 Jul;24(7):702-10.[8818565 ]
  3. Zeisel SH, DaCosta KA, Fox JG: Endogenous formation of dimethylamine. Biochem J. 1985 Dec 1;232(2):403-8.[4091797 ]
  4. NTP Toxicology and Carcinogenesis Studies of Diethanolamine (CAS No. 111-42-2) in F344/N Rats and B6C3F1 Mice (Dermal Studies). Natl Toxicol Program Tech Rep Ser. 1999 Jul;478:1-212.[12571685 ]

From T3DB


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClassOrganonitrogen compounds
SubclassAmines
Intermediate Tree NodesAlkanolamines
Direct Parent1,2-aminoalcohols
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
Substituents1,2-aminoalcohol - Secondary amine - Secondary aliphatic amine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - 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.

From ClassyFire


Targets

General Function:
Zinc ion binding
Specific Function:
Nuclear hormone receptor. The steroid hormones and their receptors are involved in the regulation of eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Ligand-dependent nuclear transactivation involves either direct homodimer binding to a palindromic estrogen response element (ERE) sequence or association with other DNA-binding transcription factors, such as AP-1/c-Jun, c-Fos, ATF-2, Sp1 and Sp3, to mediate ERE-independent signaling. Ligand binding induces a conformational change allowing subsequent or combinatorial association with multiprotein coactivator complexes through LXXLL motifs of their respective components. Mutual transrepression occurs between the estrogen receptor (ER) and NF-kappa-B in a cell-type specific manner. Decreases NF-kappa-B DNA-binding activity and inhibits NF-kappa-B-mediated transcription from the IL6 promoter and displace RELA/p65 and associated coregulators from the promoter. Recruited to the NF-kappa-B response element of the CCL2 and IL8 promoters and can displace CREBBP. Present with NF-kappa-B components RELA/p65 and NFKB1/p50 on ERE sequences. Can also act synergistically with NF-kappa-B to activate transcription involving respective recruitment adjacent response elements; the function involves CREBBP. Can activate the transcriptional activity of TFF1. Also mediates membrane-initiated estrogen signaling involving various kinase cascades. Isoform 3 is involved in activation of NOS3 and endothelial nitric oxide production. Isoforms lacking one or several functional domains are thought to modulate transcriptional activity by competitive ligand or DNA binding and/or heterodimerization with the full length receptor. Essential for MTA1-mediated transcriptional regulation of BRCA1 and BCAS3. Isoform 3 can bind to ERE and inhibit isoform 1.
Gene Name:
ESR1
Uniprot ID:
P03372
Molecular Weight:
66215.45 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 ]

From T3DB