1,3,5-Tri-tert-butylbenzene

Details

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Internal ID 8cbfb2de-0b4a-40af-bb95-6c9f521d1367
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 1,3,5-tritert-butylbenzene
SMILES (Canonical) CC(C)(C)C1=CC(=CC(=C1)C(C)(C)C)C(C)(C)C
SMILES (Isomeric) CC(C)(C)C1=CC(=CC(=C1)C(C)(C)C)C(C)(C)C
InChI InChI=1S/C18H30/c1-16(2,3)13-10-14(17(4,5)6)12-15(11-13)18(7,8)9/h10-12H,1-9H3
InChI Key GUFMBISUSZUUCB-UHFFFAOYSA-N
Popularity 154 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30
Molecular Weight 246.40 g/mol
Exact Mass 246.234750957 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.90
Atomic LogP (AlogP) 5.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1460-02-2
Benzene, 1,3,5-tris(1,1-dimethylethyl)-
1,3,5-tritert-butylbenzene
1,3,5-Tri-t-butylbenzene
Benzene, 1,3,5-tri-tert-butyl-
1,3,5-Tri-tert-butylbenzene-2-D
EINECS 215-952-4
MFCD00008831
AI3-28799
107396-03-2
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,3,5-Tri-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 + 0.7846 78.46%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.5715 57.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9650 96.50%
OATP1B3 inhibitior + 0.9573 95.73%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8929 89.29%
P-glycoprotein inhibitior - 0.9460 94.60%
P-glycoprotein substrate - 0.9814 98.14%
CYP3A4 substrate - 0.8054 80.54%
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 - 0.9659 96.59%
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 + 0.9906 99.06%
Skin irritation + 0.8812 88.12%
Skin corrosion - 0.9095 90.95%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7283 72.83%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9327 93.27%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.7208 72.08%
Nephrotoxicity + 0.6155 61.55%
Acute Oral Toxicity (c) III 0.8501 85.01%
Estrogen receptor binding - 0.6622 66.22%
Androgen receptor binding - 0.8805 88.05%
Thyroid receptor binding - 0.5521 55.21%
Glucocorticoid receptor binding - 0.6553 65.53%
Aromatase binding - 0.7557 75.57%
PPAR gamma - 0.8011 80.11%
Honey bee toxicity - 0.9536 95.36%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.8600 86.00%
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 89.26% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.62% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 85.27% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.07% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.00% 86.33%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 83.65% 97.23%

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.
Centipeda minima

Cross-Links

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PubChem 15089
NPASS NPC247986