DIETHANOLAMINE
General Information
Mainterm | DIETHANOLAMINE |
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 SDF2D Structure | |
CID | 8113 |
IUPAC Name | 2-(2-hydroxyethylamino)ethanol |
InChI | InChI=1S/C4H11NO2/c6-3-1-5-2-4-7/h5-7H,1-4H2 |
InChI Key | ZBCBWPMODOFKDW-UHFFFAOYSA-N |
Canonical SMILES | C(CO)NCCO |
Molecular Formula | C4H11NO2 |
Wikipedia | diethanolamine |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 105.137 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 4 |
Complexity | 28.9 |
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 Area | 52.5 |
Monoisotopic Mass | 105.079 |
Exact Mass | 105.079 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 7 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Isotope Atom Count | 0 |
Covalently-Bonded Unit Count | 1 |
From Pubchem
Food Additives Biosynthesis/Degradation
ADMET Predicted Profile --- Classification
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB- | 0.5676 |
Human Intestinal Absorption | HIA+ | 0.8838 |
Caco-2 Permeability | Caco2- | 0.5263 |
P-glycoprotein Substrate | Non-substrate | 0.5248 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9441 |
Non-inhibitor | 0.8358 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.7828 |
Distribution | ||
Subcellular localization | Lysosome | 0.7743 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8449 |
CYP450 2D6 Substrate | Non-substrate | 0.7818 |
CYP450 3A4 Substrate | Non-substrate | 0.7991 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.8633 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9512 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9541 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9384 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9615 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9690 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Strong inhibitor | 0.6313 |
Non-inhibitor | 0.8393 | |
AMES Toxicity | Non AMES toxic | 0.9132 |
Carcinogens | Non-carcinogens | 0.7699 |
Fish Toxicity | Low FHMT | 0.8507 |
Tetrahymena Pyriformis Toxicity | Low TPT | 0.9838 |
Honey Bee Toxicity | Low HBT | 0.5952 |
Biodegradation | Ready biodegradable | 0.7563 |
Acute Oral Toxicity | III | 0.8481 |
Carcinogenicity (Three-class) | Non-required | 0.7333 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | 0.0938 | LogS |
Caco-2 Permeability | 0.7853 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.8845 | LD50, mol/kg |
Fish Toxicity | 3.5479 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | -1.9153 | pIGC50, 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 |
|
From T3DB
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organic nitrogen compounds |
Class | Organonitrogen compounds |
Subclass | Amines |
Intermediate Tree Nodes | Alkanolamines |
Direct Parent | 1,2-aminoalcohols |
Alternative Parents | |
Molecular Framework | Aliphatic acyclic compounds |
Substituents | 1,2-aminoalcohol - Secondary amine - Secondary aliphatic amine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
Description | This 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
- 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