2-Methyl-3-phenylprop-2-enoate

Details

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Internal ID 3c481ef0-c2fe-4798-97d7-59edefde420c
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acids
IUPAC Name 2-methyl-3-phenylprop-2-enoate
SMILES (Canonical) CC(=CC1=CC=CC=C1)C(=O)[O-]
SMILES (Isomeric) CC(=CC1=CC=CC=C1)C(=O)[O-]
InChI InChI=1S/C10H10O2/c1-8(10(11)12)7-9-5-3-2-4-6-9/h2-7H,1H3,(H,11,12)/p-1
InChI Key XNCRUNXWPDJHGV-UHFFFAOYSA-M
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H9O2-
Molecular Weight 161.18 g/mol
Exact Mass 161.060254526 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 1.40
Atomic LogP (AlogP) 0.84
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methyl-3-phenylprop-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 + 0.9930 99.30%
Caco-2 + 0.8506 85.06%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6212 62.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9443 94.43%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7944 79.44%
P-glycoprotein inhibitior - 0.9908 99.08%
P-glycoprotein substrate - 0.9838 98.38%
CYP3A4 substrate - 0.7438 74.38%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8809 88.09%
CYP3A4 inhibition - 0.9446 94.46%
CYP2C9 inhibition - 0.8903 89.03%
CYP2C19 inhibition - 0.9179 91.79%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.8312 83.12%
CYP2C8 inhibition - 0.9028 90.28%
CYP inhibitory promiscuity - 0.7839 78.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5567 55.67%
Carcinogenicity (trinary) Non-required 0.6899 68.99%
Eye corrosion + 0.8220 82.20%
Eye irritation + 0.9926 99.26%
Skin irritation + 0.8370 83.70%
Skin corrosion + 0.5386 53.86%
Ames mutagenesis - 0.6424 64.24%
Human Ether-a-go-go-Related Gene inhibition - 0.8203 82.03%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.8143 81.43%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.4822 48.22%
Acute Oral Toxicity (c) III 0.9122 91.22%
Estrogen receptor binding - 0.8944 89.44%
Androgen receptor binding + 0.5366 53.66%
Thyroid receptor binding - 0.8334 83.34%
Glucocorticoid receptor binding - 0.5405 54.05%
Aromatase binding - 0.8054 80.54%
PPAR gamma - 0.6137 61.37%
Honey bee toxicity - 0.9732 97.32%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9695 96.95%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.41% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.48% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.01% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.84% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.34% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.70% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.05% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.11% 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.
Alpinia galanga
Alpinia officinarum
Etlingera elatior
Ocimum basilicum

Cross-Links

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PubChem 53433099
NPASS NPC36680