2,6-Di-t-butyl-4-hydroxytoluene

Details

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Internal ID ceaed23d-377e-450f-9784-567ae4eec3ee
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 3,5-ditert-butyl-4-methylphenol
SMILES (Canonical) CC1=C(C=C(C=C1C(C)(C)C)O)C(C)(C)C
SMILES (Isomeric) CC1=C(C=C(C=C1C(C)(C)C)O)C(C)(C)C
InChI InChI=1S/C15H24O/c1-10-12(14(2,3)4)8-11(16)9-13(10)15(5,6)7/h8-9,16H,1-7H3
InChI Key SMNGQGWPUVVORF-UHFFFAOYSA-N
Popularity 52 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.30
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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3,5-di-tert-butyl-4-methylphenol
3,5-Di-tert-butyl-p-cresol
SCHEMBL105825
CHEMBL3093613
2,6-Ditert-buthyl-4-hydroxy toluene

2D Structure

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2D Structure of 2,6-Di-t-butyl-4-hydroxytoluene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.7560 75.60%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8267 82.67%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.9293 92.93%
OATP1B3 inhibitior + 0.9718 97.18%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9218 92.18%
P-glycoprotein inhibitior - 0.9295 92.95%
P-glycoprotein substrate - 0.9700 97.00%
CYP3A4 substrate - 0.7058 70.58%
CYP2C9 substrate - 0.7461 74.61%
CYP2D6 substrate - 0.6869 68.69%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8477 84.77%
CYP2C19 inhibition - 0.8752 87.52%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition + 0.8681 86.81%
CYP2C8 inhibition - 0.8038 80.38%
CYP inhibitory promiscuity - 0.7477 74.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7019 70.19%
Carcinogenicity (trinary) Non-required 0.7295 72.95%
Eye corrosion + 0.9827 98.27%
Eye irritation + 0.9867 98.67%
Skin irritation + 0.8623 86.23%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6582 65.82%
Micronuclear - 0.8741 87.41%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.8382 83.82%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.4670 46.70%
Acute Oral Toxicity (c) III 0.8270 82.70%
Estrogen receptor binding - 0.5745 57.45%
Androgen receptor binding - 0.7569 75.69%
Thyroid receptor binding - 0.4931 49.31%
Glucocorticoid receptor binding - 0.6415 64.15%
Aromatase binding - 0.6980 69.80%
PPAR gamma - 0.7243 72.43%
Honey bee toxicity - 0.9769 97.69%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9166 91.66%

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 89.31% 98.95%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 88.09% 90.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.95% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 87.44% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.45% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.89% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.36% 93.65%

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.
Imperata cylindrica

Cross-Links

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PubChem 10220096
NPASS NPC211885