(Z)-3-(3,4-dihydroxyphenyl)prop-2-enal

Details

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Internal ID 7d645e73-7acb-426c-b9e2-bf8f7e012584
Taxonomy Phenylpropanoids and polyketides > Cinnamaldehydes
IUPAC Name (Z)-3-(3,4-dihydroxyphenyl)prop-2-enal
SMILES (Canonical) C1=CC(=C(C=C1C=CC=O)O)O
SMILES (Isomeric) C1=CC(=C(C=C1/C=C\C=O)O)O
InChI InChI=1S/C9H8O3/c10-5-1-2-7-3-4-8(11)9(12)6-7/h1-6,11-12H/b2-1-
InChI Key AXMVYSVVTMKQSL-UPHRSURJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O3
Molecular Weight 164.16 g/mol
Exact Mass 164.047344113 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.31
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-3-(3,4-dihydroxyphenyl)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 + 0.9936 99.36%
Caco-2 + 0.8611 86.11%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8092 80.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9570 95.70%
OATP1B3 inhibitior + 0.9757 97.57%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9205 92.05%
P-glycoprotein inhibitior - 0.9881 98.81%
P-glycoprotein substrate - 0.9896 98.96%
CYP3A4 substrate - 0.7294 72.94%
CYP2C9 substrate - 0.5959 59.59%
CYP2D6 substrate - 0.8138 81.38%
CYP3A4 inhibition - 0.8281 82.81%
CYP2C9 inhibition - 0.8493 84.93%
CYP2C19 inhibition - 0.8781 87.81%
CYP2D6 inhibition - 0.9382 93.82%
CYP1A2 inhibition - 0.7494 74.94%
CYP2C8 inhibition - 0.8737 87.37%
CYP inhibitory promiscuity - 0.7077 70.77%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.7723 77.23%
Carcinogenicity (trinary) Warning 0.4833 48.33%
Eye corrosion + 0.8554 85.54%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9359 93.59%
Skin corrosion + 0.5846 58.46%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8092 80.92%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.5984 59.84%
skin sensitisation + 0.9743 97.43%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.7342 73.42%
Acute Oral Toxicity (c) III 0.7016 70.16%
Estrogen receptor binding - 0.5133 51.33%
Androgen receptor binding + 0.7304 73.04%
Thyroid receptor binding - 0.5874 58.74%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.6077 60.77%
PPAR gamma + 0.6155 61.55%
Honey bee toxicity - 0.9271 92.71%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9550 95.50%

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 98.34% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.70% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.61% 95.56%
CHEMBL3194 P02766 Transthyretin 93.36% 90.71%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.66% 93.40%
CHEMBL1929 P47989 Xanthine dehydrogenase 86.11% 96.12%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.09% 96.00%
CHEMBL4208 P20618 Proteasome component C5 84.89% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.60% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.49% 99.15%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 84.45% 80.78%
CHEMBL3401 O75469 Pregnane X receptor 83.65% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.86% 89.00%

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.
Syagrus romanzoffiana

Cross-Links

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PubChem 131468559
LOTUS LTS0208643
wikiData Q104920652