3-Ethylphenol
Relevant Data
Food Additives Approved in the United States:
General Information
Chemical name | 3-Ethylphenol |
CAS number | 620-17-7 |
COE number | 549 |
Flavouring type | substances |
FL No. | 04.021 |
Mixture | No |
Purity of the named substance at least 95% unless otherwise specified |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF2D Structure | |
CID | 12101 |
IUPAC Name | 3-ethylphenol |
InChI | InChI=1S/C8H10O/c1-2-7-4-3-5-8(9)6-7/h3-6,9H,2H2,1H3 |
InChI Key | HMNKTRSOROOSPP-UHFFFAOYSA-N |
Canonical SMILES | CCC1=CC(=CC=C1)O |
Molecular Formula | C8H10O |
Wikipedia | 3-ethylphenol |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 122.167 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 1 |
Complexity | 80.6 |
CACTVS Substructure Key Fingerprint | A A A D c c B w I 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 w A A A A A A A A A A A B A A A A G g A A C A A A D A S A m A A y B o A A A g C A A i B C A A A C A A A g I A A I i A A G C I g I J i K C E R K A c A A k w B E I m A e A w L A O A A A B A A A A A A A A A A I A A A A A A A A A A A A A A A = = |
Topological Polar Surface Area | 20.2 |
Monoisotopic Mass | 122.073 |
Exact Mass | 122.073 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 9 |
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
ADMET Predicted Profile --- Classification
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB+ | 0.9076 |
Human Intestinal Absorption | HIA+ | 0.9948 |
Caco-2 Permeability | Caco2+ | 0.8868 |
P-glycoprotein Substrate | Non-substrate | 0.6761 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9675 |
Non-inhibitor | 0.9662 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8721 |
Distribution | ||
Subcellular localization | Mitochondria | 0.7384 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.7108 |
CYP450 2D6 Substrate | Non-substrate | 0.8666 |
CYP450 3A4 Substrate | Non-substrate | 0.7014 |
CYP450 1A2 Inhibitor | Inhibitor | 0.6932 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.7645 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9333 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.6572 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.8252 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6214 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7889 |
Non-inhibitor | 0.9376 | |
AMES Toxicity | Non AMES toxic | 0.9470 |
Carcinogens | Non-carcinogens | 0.6717 |
Fish Toxicity | High FHMT | 0.7973 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9798 |
Honey Bee Toxicity | High HBT | 0.8192 |
Biodegradation | Not ready biodegradable | 0.5987 |
Acute Oral Toxicity | III | 0.4678 |
Carcinogenicity (Three-class) | Non-required | 0.5872 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -1.3170 | LogS |
Caco-2 Permeability | 1.6122 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.2622 | LD50, mol/kg |
Fish Toxicity | 1.0934 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.2007 | pIGC50, ug/L |
From admetSAR
Toxicity Profile
Route of Exposure | |
---|---|
Mechanism of Toxicity | |
Metabolism | |
Toxicity Values | |
Lethal Dose | |
Carcinogenicity (IARC Classification) | No indication of carcinogenicity to humans (not listed by IARC). |
Minimum Risk Level | |
Health Effects | |
Treatment | |
Reference |
|
From T3DB
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Benzenoids |
Class | Phenols |
Subclass | 1-hydroxy-4-unsubstituted benzenoids |
Intermediate Tree Nodes | Not available |
Direct Parent | 1-hydroxy-4-unsubstituted benzenoids |
Alternative Parents | |
Molecular Framework | Aromatic homomonocyclic compounds |
Substituents | 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
Description | This compound belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position. |
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