Methyl p-methoxycinnamate

Details

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Internal ID 955ae40c-7890-42fd-a481-072d5e6c1199
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid esters
IUPAC Name methyl 3-(4-methoxyphenyl)prop-2-enoate
SMILES (Canonical) COC1=CC=C(C=C1)C=CC(=O)OC
SMILES (Isomeric) COC1=CC=C(C=C1)C=CC(=O)OC
InChI InChI=1S/C11H12O3/c1-13-10-6-3-9(4-7-10)5-8-11(12)14-2/h3-8H,1-2H3
InChI Key VEZIKIAGFYZTCI-UHFFFAOYSA-N
Popularity 33 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O3
Molecular Weight 192.21 g/mol
Exact Mass 192.078644241 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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methyl 3-(4-methoxyphenyl)prop-2-enoate
4-Methoxycinnamate methyl ester
p-Methoxymethylcinnamate
(E)-Methyl 4-methoxycinnamate
METHYL-4-METHOXYCINNAMATE
EINECS 212-614-8
NSC 26461
methyl-p-methoxycinnamate
VEZIKIAGFYZTCI-UHFFFAOYSA-N
DTXSID401312296
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methyl p-methoxycinnamate

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 + 0.9303 93.03%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8802 88.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9642 96.42%
OATP1B3 inhibitior + 0.9778 97.78%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6918 69.18%
P-glycoprotein inhibitior - 0.9691 96.91%
P-glycoprotein substrate - 0.9801 98.01%
CYP3A4 substrate - 0.6260 62.60%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8434 84.34%
CYP3A4 inhibition - 0.9002 90.02%
CYP2C9 inhibition - 0.9526 95.26%
CYP2C19 inhibition - 0.8193 81.93%
CYP2D6 inhibition - 0.9733 97.33%
CYP1A2 inhibition + 0.6757 67.57%
CYP2C8 inhibition - 0.8561 85.61%
CYP inhibitory promiscuity - 0.7207 72.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5984 59.84%
Carcinogenicity (trinary) Non-required 0.6233 62.33%
Eye corrosion + 0.7418 74.18%
Eye irritation + 0.9907 99.07%
Skin irritation + 0.6479 64.79%
Skin corrosion - 0.9825 98.25%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5972 59.72%
Micronuclear - 0.6326 63.26%
Hepatotoxicity - 0.7019 70.19%
skin sensitisation - 0.7138 71.38%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.5660 56.60%
Acute Oral Toxicity (c) III 0.8816 88.16%
Estrogen receptor binding - 0.5904 59.04%
Androgen receptor binding + 0.5492 54.92%
Thyroid receptor binding - 0.7952 79.52%
Glucocorticoid receptor binding - 0.7062 70.62%
Aromatase binding + 0.5717 57.17%
PPAR gamma - 0.9027 90.27%
Honey bee toxicity - 0.9729 97.29%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9425 94.25%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.36% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.00% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.20% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.70% 96.09%
CHEMBL4208 P20618 Proteasome component C5 91.31% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 89.28% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.20% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.29% 99.17%

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.
Gmelina asiatica
Philotheca obovalis
Scrophularia buergeriana
Sideritis infernalis

Cross-Links

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PubChem 92841
LOTUS LTS0036328
wikiData Q104199299