3,4,5-Trimethoxycinnamaldehyde, (E)-

Details

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Internal ID 795cb420-d209-40ca-82b0-0a734daf0c7c
Taxonomy Phenylpropanoids and polyketides > Cinnamaldehydes
IUPAC Name (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O4/c1-14-10-7-9(5-4-6-13)8-11(15-2)12(10)16-3/h4-8H,1-3H3/b5-4+
InChI Key XDSHNNRBLSBDAP-SNAWJCMRSA-N
Popularity 13 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 1.30
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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71277-13-9
34346-90-2
(E)-3,4,5-Trimethoxycinnamaldehyde
3,4,5-Trimethoxycinnamic aldehyde
2-Propenal, 3-(3,4,5-trimethoxyphenyl)-, (2E)-
UNII-0U9SB79TM1
trans-3,4,5-Trimethoxycinnamaldehyde
(E)-3-(3,4,5-trimethoxyphenyl)prop-2-enal
3,4,5-Trimethoxycinnamaldehyde, (E)-
0U9SB79TM1
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4,5-Trimethoxycinnamaldehyde, (E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.8310 83.10%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7925 79.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9324 93.24%
OATP1B3 inhibitior + 0.9875 98.75%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7647 76.47%
P-glycoprotein inhibitior - 0.9615 96.15%
P-glycoprotein substrate - 0.9712 97.12%
CYP3A4 substrate - 0.6260 62.60%
CYP2C9 substrate + 0.5954 59.54%
CYP2D6 substrate - 0.7817 78.17%
CYP3A4 inhibition - 0.5513 55.13%
CYP2C9 inhibition - 0.9850 98.50%
CYP2C19 inhibition - 0.6199 61.99%
CYP2D6 inhibition - 0.9537 95.37%
CYP1A2 inhibition + 0.6673 66.73%
CYP2C8 inhibition - 0.7032 70.32%
CYP inhibitory promiscuity + 0.5633 56.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7914 79.14%
Carcinogenicity (trinary) Non-required 0.5944 59.44%
Eye corrosion + 0.5236 52.36%
Eye irritation + 0.9511 95.11%
Skin irritation - 0.6292 62.92%
Skin corrosion - 0.9785 97.85%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4591 45.91%
Micronuclear + 0.5133 51.33%
Hepatotoxicity + 0.5803 58.03%
skin sensitisation - 0.7988 79.88%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.5784 57.84%
Acute Oral Toxicity (c) III 0.6177 61.77%
Estrogen receptor binding - 0.6204 62.04%
Androgen receptor binding - 0.6782 67.82%
Thyroid receptor binding - 0.6547 65.47%
Glucocorticoid receptor binding - 0.8302 83.02%
Aromatase binding - 0.6127 61.27%
PPAR gamma - 0.8679 86.79%
Honey bee toxicity - 0.7985 79.85%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9521 95.21%

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 95.69% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.35% 95.56%
CHEMBL4302 P08183 P-glycoprotein 1 88.55% 92.98%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.00% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.99% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.46% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.03% 91.11%

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.
Amburana cearensis
Boronia pinnata
Zanthoxylum nitidum

Cross-Links

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PubChem 5839209
LOTUS LTS0004819
wikiData Q27237259