4-Tert-butyl-1-(4-tert-butyl-2-ethylphenoxy)-2-ethylbenzene

Details

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Internal ID 7cdd8221-2417-4a97-a21a-fbe7f4694c0b
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name 4-tert-butyl-1-(4-tert-butyl-2-ethylphenoxy)-2-ethylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H34O/c1-9-17-15-19(23(3,4)5)11-13-21(17)25-22-14-12-20(24(6,7)8)16-18(22)10-2/h11-16H,9-10H2,1-8H3
InChI Key HUHYPGHUVADQQH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H34O
Molecular Weight 338.50 g/mol
Exact Mass 338.260965704 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 8.40
Atomic LogP (AlogP) 7.20
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Tert-butyl-1-(4-tert-butyl-2-ethylphenoxy)-2-ethylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8387 83.87%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.8472 84.72%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9557 95.57%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9088 90.88%
P-glycoprotein inhibitior + 0.6095 60.95%
P-glycoprotein substrate - 0.9361 93.61%
CYP3A4 substrate - 0.6499 64.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6684 66.84%
CYP3A4 inhibition - 0.8140 81.40%
CYP2C9 inhibition + 0.8085 80.85%
CYP2C19 inhibition + 0.9124 91.24%
CYP2D6 inhibition - 0.9061 90.61%
CYP1A2 inhibition + 0.9158 91.58%
CYP2C8 inhibition - 0.6153 61.53%
CYP inhibitory promiscuity + 0.8950 89.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6319 63.19%
Carcinogenicity (trinary) Non-required 0.5370 53.70%
Eye corrosion - 0.7680 76.80%
Eye irritation + 0.8287 82.87%
Skin irritation - 0.9019 90.19%
Skin corrosion - 0.9339 93.39%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8947 89.47%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.6753 67.53%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.5790 57.90%
Acute Oral Toxicity (c) III 0.7279 72.79%
Estrogen receptor binding + 0.9183 91.83%
Androgen receptor binding + 0.6065 60.65%
Thyroid receptor binding + 0.8625 86.25%
Glucocorticoid receptor binding + 0.6705 67.05%
Aromatase binding + 0.7560 75.60%
PPAR gamma + 0.7265 72.65%
Honey bee toxicity - 0.9123 91.23%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9919 99.19%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 94.71% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.64% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.21% 96.09%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 88.73% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.42% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 85.34% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.31% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.81% 99.17%
CHEMBL3232685 O00257 E3 SUMO-protein ligase CBX4 82.60% 93.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.36% 89.62%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.34% 92.68%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.84% 96.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.12% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Basella alba

Cross-Links

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PubChem 163192399
LOTUS LTS0164852
wikiData Q105033793