(4-Methyl-2-propan-2-ylphenyl) 2-methylbut-2-enoate

Details

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Internal ID 8d1771f6-5a41-49ee-97f9-0d2a2b7e9b21
Taxonomy Benzenoids > Phenol esters
IUPAC Name (4-methyl-2-propan-2-ylphenyl) 2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O2/c1-6-12(5)15(16)17-14-8-7-11(4)9-13(14)10(2)3/h6-10H,1-5H3
InChI Key KRVQPLGJQFNMHY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.99
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4-Methyl-2-propan-2-ylphenyl) 2-methylbut-2-enoate

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 + 0.8828 88.28%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8953 89.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9432 94.32%
OATP1B3 inhibitior + 0.9731 97.31%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5715 57.15%
P-glycoprotein inhibitior - 0.9170 91.70%
P-glycoprotein substrate - 0.9076 90.76%
CYP3A4 substrate - 0.5772 57.72%
CYP2C9 substrate - 0.5735 57.35%
CYP2D6 substrate - 0.8900 89.00%
CYP3A4 inhibition - 0.9013 90.13%
CYP2C9 inhibition - 0.8494 84.94%
CYP2C19 inhibition + 0.7586 75.86%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition + 0.8472 84.72%
CYP2C8 inhibition - 0.8933 89.33%
CYP inhibitory promiscuity + 0.7553 75.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6832 68.32%
Carcinogenicity (trinary) Non-required 0.6071 60.71%
Eye corrosion - 0.7480 74.80%
Eye irritation + 0.6137 61.37%
Skin irritation - 0.6315 63.15%
Skin corrosion - 0.9790 97.90%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7977 79.77%
Micronuclear - 0.7226 72.26%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.7876 78.76%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.6254 62.54%
Acute Oral Toxicity (c) III 0.8578 85.78%
Estrogen receptor binding + 0.5621 56.21%
Androgen receptor binding - 0.7328 73.28%
Thyroid receptor binding + 0.5461 54.61%
Glucocorticoid receptor binding - 0.7414 74.14%
Aromatase binding + 0.7219 72.19%
PPAR gamma - 0.7105 71.05%
Honey bee toxicity - 0.7006 70.06%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5707 57.07%
Fish aquatic toxicity + 0.9934 99.34%

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
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 93.34% 97.21%
CHEMBL2581 P07339 Cathepsin D 91.61% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.46% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.01% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.96% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.23% 89.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.81% 96.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.77% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.09% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.08% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.95% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.35% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.29% 90.71%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 80.50% 97.53%

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.
Bishovia boliviensis

Cross-Links

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PubChem 162982939
LOTUS LTS0250142
wikiData Q105145266