3-Methoxy-cuminyl isobutyrate

Details

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Internal ID 34200784-6d2d-4c2e-b292-9e0c7cb4942e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name (3-methoxy-4-propan-2-ylphenyl)methyl 2-methylpropanoate
SMILES (Canonical) CC(C)C1=C(C=C(C=C1)COC(=O)C(C)C)OC
SMILES (Isomeric) CC(C)C1=C(C=C(C=C1)COC(=O)C(C)C)OC
InChI InChI=1S/C15H22O3/c1-10(2)13-7-6-12(8-14(13)17-5)9-18-15(16)11(3)4/h6-8,10-11H,9H2,1-5H3
InChI Key JVOZDVTWETUPPI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O3
Molecular Weight 250.33 g/mol
Exact Mass 250.15689456 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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JVOZDVTWETUPPI-UHFFFAOYSA-N

2D Structure

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2D Structure of 3-Methoxy-cuminyl isobutyrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.8078 80.78%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.9410 94.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9390 93.90%
OATP1B3 inhibitior + 0.9635 96.35%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5438 54.38%
P-glycoprotein inhibitior - 0.9269 92.69%
P-glycoprotein substrate - 0.8256 82.56%
CYP3A4 substrate - 0.5355 53.55%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.9250 92.50%
CYP2C9 inhibition - 0.7990 79.90%
CYP2C19 inhibition - 0.8075 80.75%
CYP2D6 inhibition - 0.9454 94.54%
CYP1A2 inhibition + 0.7211 72.11%
CYP2C8 inhibition - 0.5648 56.48%
CYP inhibitory promiscuity - 0.5460 54.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6392 63.92%
Carcinogenicity (trinary) Non-required 0.5890 58.90%
Eye corrosion - 0.8162 81.62%
Eye irritation + 0.6554 65.54%
Skin irritation - 0.7816 78.16%
Skin corrosion - 0.9836 98.36%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7456 74.56%
Micronuclear - 0.8552 85.52%
Hepatotoxicity - 0.5670 56.70%
skin sensitisation - 0.7897 78.97%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6324 63.24%
Acute Oral Toxicity (c) III 0.8071 80.71%
Estrogen receptor binding + 0.7359 73.59%
Androgen receptor binding - 0.5841 58.41%
Thyroid receptor binding - 0.6922 69.22%
Glucocorticoid receptor binding - 0.6542 65.42%
Aromatase binding + 0.6359 63.59%
PPAR gamma - 0.8449 84.49%
Honey bee toxicity - 0.7994 79.94%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5155 51.55%
Fish aquatic toxicity + 0.9585 95.85%

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 98.24% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.25% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.94% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.54% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.70% 91.11%
CHEMBL2535 P11166 Glucose transporter 88.67% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.80% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.10% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.92% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.80% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.46% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.42% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.13% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.74% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.54% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.57% 96.00%

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.
Abrus precatorius
Dittrichia viscosa subsp. viscosa
Garcinia multiflora
Pulicaria dysenterica

Cross-Links

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PubChem 91751362
NPASS NPC312479
LOTUS LTS0143029
wikiData Q105135879