(4-Methyl-2-propan-2-ylphenyl) 3-methylbutanoate

Details

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Internal ID 737b95da-5555-4e5e-b791-225623072d44
Taxonomy Benzenoids > Phenol esters
IUPAC Name (4-methyl-2-propan-2-ylphenyl) 3-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-10(2)8-15(16)17-14-7-6-12(5)9-13(14)11(3)4/h6-7,9-11H,8H2,1-5H3
InChI Key UUWAUYJLHCWFPZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

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) 3-methylbutanoate

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 + 0.8293 82.93%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.9219 92.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.4689 46.89%
P-glycoprotein inhibitior - 0.9151 91.51%
P-glycoprotein substrate - 0.8856 88.56%
CYP3A4 substrate - 0.6078 60.78%
CYP2C9 substrate - 0.6071 60.71%
CYP2D6 substrate - 0.8427 84.27%
CYP3A4 inhibition - 0.9548 95.48%
CYP2C9 inhibition - 0.8441 84.41%
CYP2C19 inhibition - 0.6874 68.74%
CYP2D6 inhibition - 0.8495 84.95%
CYP1A2 inhibition + 0.8633 86.33%
CYP2C8 inhibition - 0.9177 91.77%
CYP inhibitory promiscuity - 0.7196 71.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6561 65.61%
Carcinogenicity (trinary) Non-required 0.5603 56.03%
Eye corrosion + 0.4541 45.41%
Eye irritation + 0.6655 66.55%
Skin irritation - 0.7540 75.40%
Skin corrosion - 0.9526 95.26%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6438 64.38%
Micronuclear - 0.8551 85.51%
Hepatotoxicity + 0.6784 67.84%
skin sensitisation + 0.8085 80.85%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4629 46.29%
Acute Oral Toxicity (c) III 0.7669 76.69%
Estrogen receptor binding - 0.8071 80.71%
Androgen receptor binding - 0.7001 70.01%
Thyroid receptor binding - 0.6691 66.91%
Glucocorticoid receptor binding - 0.8519 85.19%
Aromatase binding - 0.6815 68.15%
PPAR gamma - 0.8086 80.86%
Honey bee toxicity - 0.8817 88.17%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5807 58.07%
Fish aquatic toxicity + 0.9724 97.24%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.22% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.52% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 92.18% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.76% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.64% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.21% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.14% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.17% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.07% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.96% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.37% 86.33%

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.
Callilepis salicifolia

Cross-Links

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PubChem 163031902
LOTUS LTS0165736
wikiData Q105279627