3-(tert-Butoxy)-4-isopropyltoluene

Details

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Internal ID e0665331-c28c-420e-be72-38cc26aee452
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 4-methyl-2-[(2-methylpropan-2-yl)oxy]-1-propan-2-ylbenzene
SMILES (Canonical) CC1=CC(=C(C=C1)C(C)C)OC(C)(C)C
SMILES (Isomeric) CC1=CC(=C(C=C1)C(C)C)OC(C)(C)C
InChI InChI=1S/C14H22O/c1-10(2)12-8-7-11(3)9-13(12)15-14(4,5)6/h7-10H,1-6H3
InChI Key HFHSHFJHABRKEP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O
Molecular Weight 206.32 g/mol
Exact Mass 206.167065321 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.30
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2-(tert-Butoxy)-1-isopropyl-4-methylbenzene
3-(tert-Butoxy)-4-isopropyltoluene
SCHEMBL16812865
MFCD29103502
SY298726

2D Structure

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2D Structure of 3-(tert-Butoxy)-4-isopropyltoluene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8510 85.10%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8273 82.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9629 96.29%
OATP1B3 inhibitior + 0.9765 97.65%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8415 84.15%
P-glycoprotein inhibitior - 0.9622 96.22%
P-glycoprotein substrate - 0.9410 94.10%
CYP3A4 substrate - 0.5827 58.27%
CYP2C9 substrate - 0.5665 56.65%
CYP2D6 substrate + 0.3822 38.22%
CYP3A4 inhibition - 0.8570 85.70%
CYP2C9 inhibition - 0.8470 84.70%
CYP2C19 inhibition - 0.6533 65.33%
CYP2D6 inhibition - 0.9365 93.65%
CYP1A2 inhibition + 0.8731 87.31%
CYP2C8 inhibition - 0.8708 87.08%
CYP inhibitory promiscuity - 0.5536 55.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7019 70.19%
Carcinogenicity (trinary) Non-required 0.5325 53.25%
Eye corrosion + 0.9468 94.68%
Eye irritation + 0.9404 94.04%
Skin irritation + 0.5870 58.70%
Skin corrosion + 0.5435 54.35%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3930 39.30%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.7382 73.82%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.6507 65.07%
Acute Oral Toxicity (c) III 0.7796 77.96%
Estrogen receptor binding - 0.6134 61.34%
Androgen receptor binding - 0.8412 84.12%
Thyroid receptor binding - 0.7213 72.13%
Glucocorticoid receptor binding - 0.8415 84.15%
Aromatase binding - 0.7057 70.57%
PPAR gamma - 0.8141 81.41%
Honey bee toxicity - 0.8122 81.22%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.9469 94.69%

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
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 92.20% 97.23%
CHEMBL2581 P07339 Cathepsin D 91.99% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 90.44% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.81% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.08% 93.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 87.03% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.00% 89.62%
CHEMBL4581 P52732 Kinesin-like protein 1 85.81% 93.18%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.28% 91.11%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.67% 93.65%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.52% 90.93%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.16% 97.21%

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.
Mikania luetzelburgii

Cross-Links

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PubChem 118155638
LOTUS LTS0262974
wikiData Q105027343