Methyl trans-3-Hydroxycinnamate

Details

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Internal ID 333eb7c1-0753-4cc6-b361-3db5ce719272
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acid esters > Coumaric acid esters
IUPAC Name methyl (E)-3-(3-hydroxyphenyl)prop-2-enoate
SMILES (Canonical) COC(=O)C=CC1=CC(=CC=C1)O
SMILES (Isomeric) COC(=O)/C=C/C1=CC(=CC=C1)O
InChI InChI=1S/C10H10O3/c1-13-10(12)6-5-8-3-2-4-9(11)7-8/h2-7,11H,1H3/b6-5+
InChI Key PKALKWFZXXGNJD-AATRIKPKSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O3
Molecular Weight 178.18 g/mol
Exact Mass 178.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.58
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Methyl trans-3-Hydroxycinnamate
3-Hydroxycinnamic acid methyl ester
methyl 3-(3-hydroxyphenyl)prop-2-enoate
3943-95-1
2-Propenoic acid, 3-(3-hydroxyphenyl)-, methyl ester, (2E)-
Methyl 3-(3-hydroxyphenyl)acrylate
methyl (E)-3-(3-hydroxyphenyl)prop-2-enoate
trans-3-(3-hydroxyphenyl)acrylic acid methyl ester
2-Propenoic acid, 3-(3-hydroxyphenyl)-, methyl ester
methyl (2E)-3-(3-hydroxyphenyl)prop-2-enoate
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 trans-3-Hydroxycinnamate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.8834 88.34%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8702 87.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9391 93.91%
OATP1B3 inhibitior + 0.9789 97.89%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6660 66.60%
P-glycoprotein inhibitior - 0.9841 98.41%
P-glycoprotein substrate - 0.9179 91.79%
CYP3A4 substrate - 0.5918 59.18%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8578 85.78%
CYP3A4 inhibition - 0.9401 94.01%
CYP2C9 inhibition - 0.9472 94.72%
CYP2C19 inhibition - 0.8758 87.58%
CYP2D6 inhibition - 0.9796 97.96%
CYP1A2 inhibition - 0.5932 59.32%
CYP2C8 inhibition + 0.5500 55.00%
CYP inhibitory promiscuity - 0.9115 91.15%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.5730 57.30%
Carcinogenicity (trinary) Non-required 0.5631 56.31%
Eye corrosion + 0.6362 63.62%
Eye irritation + 0.9943 99.43%
Skin irritation + 0.7975 79.75%
Skin corrosion - 0.9094 90.94%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6469 64.69%
Micronuclear - 0.5045 50.45%
Hepatotoxicity - 0.6726 67.26%
skin sensitisation - 0.8177 81.77%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.6946 69.46%
Acute Oral Toxicity (c) III 0.8002 80.02%
Estrogen receptor binding - 0.6127 61.27%
Androgen receptor binding + 0.5352 53.52%
Thyroid receptor binding - 0.7804 78.04%
Glucocorticoid receptor binding - 0.6556 65.56%
Aromatase binding - 0.6190 61.90%
PPAR gamma - 0.7854 78.54%
Honey bee toxicity - 0.9480 94.80%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8953 89.53%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.85% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.62% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.61% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.23% 96.00%
CHEMBL2581 P07339 Cathepsin D 89.97% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.36% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.09% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.04% 99.17%
CHEMBL2535 P11166 Glucose transporter 86.47% 98.75%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.14% 100.00%
CHEMBL4208 P20618 Proteasome component C5 80.00% 90.00%

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.
Typha angustifolia
Typha orientalis

Cross-Links

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PubChem 5352910
NPASS NPC94343