3-(2,4,6-Trimethoxyphenyl)prop-2-enal

Details

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Internal ID f8edb3ef-c758-4adb-ab3b-bcae931f01cd
Taxonomy Phenylpropanoids and polyketides > Cinnamaldehydes
IUPAC Name (E)-3-(2,4,6-trimethoxyphenyl)prop-2-enal
SMILES (Canonical) COC1=CC(=C(C(=C1)OC)C=CC=O)OC
SMILES (Isomeric) COC1=CC(=C(C(=C1)OC)/C=C/C=O)OC
InChI InChI=1S/C12H14O4/c1-14-9-7-11(15-2)10(5-4-6-13)12(8-9)16-3/h4-8H,1-3H3/b5-4+
InChI Key ZHRKDNDVZCPRBF-SNAWJCMRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O4
Molecular Weight 222.24 g/mol
Exact Mass 222.08920892 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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3-(2,4,6-trimethoxyphenyl)prop-2-enal
EN300-1853065
261967-09-3

2D Structure

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2D Structure of 3-(2,4,6-Trimethoxyphenyl)prop-2-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.7944 79.44%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8524 85.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9157 91.57%
OATP1B3 inhibitior + 0.9900 99.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6865 68.65%
P-glycoprotein inhibitior - 0.9578 95.78%
P-glycoprotein substrate - 0.9644 96.44%
CYP3A4 substrate - 0.6464 64.64%
CYP2C9 substrate + 0.5954 59.54%
CYP2D6 substrate - 0.7817 78.17%
CYP3A4 inhibition - 0.5404 54.04%
CYP2C9 inhibition - 0.9781 97.81%
CYP2C19 inhibition - 0.6432 64.32%
CYP2D6 inhibition - 0.9618 96.18%
CYP1A2 inhibition + 0.7352 73.52%
CYP2C8 inhibition - 0.8613 86.13%
CYP inhibitory promiscuity + 0.6413 64.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7149 71.49%
Carcinogenicity (trinary) Non-required 0.6394 63.94%
Eye corrosion + 0.5188 51.88%
Eye irritation + 0.9706 97.06%
Skin irritation - 0.6586 65.86%
Skin corrosion - 0.9858 98.58%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.5167 51.67%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8197 81.97%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.5584 55.84%
Acute Oral Toxicity (c) III 0.6161 61.61%
Estrogen receptor binding - 0.6647 66.47%
Androgen receptor binding - 0.5890 58.90%
Thyroid receptor binding - 0.6702 67.02%
Glucocorticoid receptor binding - 0.6661 66.61%
Aromatase binding - 0.4888 48.88%
PPAR gamma - 0.6866 68.66%
Honey bee toxicity - 0.8892 88.92%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9662 96.62%

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 96.16% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.75% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.27% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.46% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.24% 86.33%
CHEMBL4208 P20618 Proteasome component C5 83.04% 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.
Siphoneugena densiflora

Cross-Links

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PubChem 10536994
LOTUS LTS0059216
wikiData Q105375967