2-Methylbutyl 3-phenylpropanoate

Details

Top
Internal ID 671a7391-f6fc-4c12-991e-281d1f089599
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name 2-methylbutyl 3-phenylpropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H20O2/c1-3-12(2)11-16-14(15)10-9-13-7-5-4-6-8-13/h4-8,12H,3,9-11H2,1-2H3
InChI Key VZQROVHKJNZZDN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H20O2
Molecular Weight 220.31 g/mol
Exact Mass 220.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

Top
SCHEMBL19024791
VZQROVHKJNZZDN-UHFFFAOYSA-N
2-Methylbutyl-3-phenyl-propionate
3-Phenylpropionic acid, 2-methylbutyl ester

2D Structure

Top
2D Structure of 2-Methylbutyl 3-phenylpropanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9642 96.42%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5467 54.67%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.8812 88.12%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6450 64.50%
P-glycoprotein inhibitior - 0.9353 93.53%
P-glycoprotein substrate - 0.8063 80.63%
CYP3A4 substrate - 0.6056 60.56%
CYP2C9 substrate - 0.6071 60.71%
CYP2D6 substrate - 0.8427 84.27%
CYP3A4 inhibition - 0.8931 89.31%
CYP2C9 inhibition - 0.8566 85.66%
CYP2C19 inhibition - 0.7195 71.95%
CYP2D6 inhibition - 0.8815 88.15%
CYP1A2 inhibition + 0.6819 68.19%
CYP2C8 inhibition - 0.8681 86.81%
CYP inhibitory promiscuity - 0.6908 69.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6088 60.88%
Eye corrosion + 0.5680 56.80%
Eye irritation + 0.5481 54.81%
Skin irritation - 0.7406 74.06%
Skin corrosion - 0.9950 99.50%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6731 67.31%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5231 52.31%
skin sensitisation + 0.6022 60.22%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7806 78.06%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity - 0.8536 85.36%
Acute Oral Toxicity (c) III 0.8343 83.43%
Estrogen receptor binding - 0.8449 84.49%
Androgen receptor binding - 0.7999 79.99%
Thyroid receptor binding - 0.5958 59.58%
Glucocorticoid receptor binding - 0.7612 76.12%
Aromatase binding - 0.7461 74.61%
PPAR gamma - 0.8503 85.03%
Honey bee toxicity - 0.8792 87.92%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5655 56.55%
Fish aquatic toxicity + 0.9917 99.17%

Targets

Top

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 97.59% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.50% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 93.75% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.61% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.15% 99.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.44% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.14% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.92% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 85.41% 94.73%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.15% 100.00%

Plants that contains it

Top
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.
Baccharis dracunculifolia

Cross-Links

Top
PubChem 6429045
LOTUS LTS0168725
wikiData Q104667239