1,3-Di-tert-butylbenzene

Details

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Internal ID 1b9f3831-f8dc-4b37-ba02-b421f168d47e
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 1,3-ditert-butylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22/c1-13(2,3)11-8-7-9-12(10-11)14(4,5)6/h7-10H,1-6H3
InChI Key ILNDSSCEZZFNGE-UHFFFAOYSA-N
Popularity 96 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22
Molecular Weight 190.32 g/mol
Exact Mass 190.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.28
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1014-60-4
Benzene, 1,3-bis(1,1-dimethylethyl)-
1,3-ditert-butylbenzene
Benzene, m-di-tert-butyl-
m-Di-tert-butylbenzene
1,3-di-t-butylbenzene
1,3-bis(1,1-dimethylethyl)benzene
MFCD00008830
NSC243654
1,3-ditert-butyl-benzene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,3-Di-tert-butylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.8747 87.47%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.5715 57.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9671 96.71%
OATP1B3 inhibitior + 0.9573 95.73%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9028 90.28%
P-glycoprotein inhibitior - 0.9732 97.32%
P-glycoprotein substrate - 0.9427 94.27%
CYP3A4 substrate - 0.7736 77.36%
CYP2C9 substrate - 0.8253 82.53%
CYP2D6 substrate - 0.7309 73.09%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8944 89.44%
CYP2C19 inhibition - 0.9658 96.58%
CYP2D6 inhibition - 0.9394 93.94%
CYP1A2 inhibition - 0.8698 86.98%
CYP2C8 inhibition - 0.8650 86.50%
CYP inhibitory promiscuity - 0.8028 80.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5236 52.36%
Carcinogenicity (trinary) Warning 0.5519 55.19%
Eye corrosion + 0.9802 98.02%
Eye irritation + 0.9885 98.85%
Skin irritation + 0.8812 88.12%
Skin corrosion - 0.9095 90.95%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7264 72.64%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.9327 93.27%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.7208 72.08%
Nephrotoxicity + 0.5327 53.27%
Acute Oral Toxicity (c) III 0.8501 85.01%
Estrogen receptor binding - 0.7475 74.75%
Androgen receptor binding - 0.9148 91.48%
Thyroid receptor binding - 0.7221 72.21%
Glucocorticoid receptor binding - 0.7558 75.58%
Aromatase binding - 0.8188 81.88%
PPAR gamma - 0.8219 82.19%
Honey bee toxicity - 0.9703 97.03%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.8200 82.00%
Fish aquatic toxicity + 0.9254 92.54%

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 94.99% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.86% 86.33%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 89.75% 97.23%
CHEMBL3401 O75469 Pregnane X receptor 87.90% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.84% 95.56%
CHEMBL2039 P27338 Monoamine oxidase B 85.72% 92.51%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 84.54% 81.29%
CHEMBL1907 P15144 Aminopeptidase N 84.31% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.58% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 136810
LOTUS LTS0266322
wikiData Q27160875