(Z)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid

Details

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Internal ID e25894a9-faeb-48e9-a32c-e47607cb334d
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acids
IUPAC Name (Z)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid
SMILES (Canonical) COC1=CC(=C(C=C1)C=CC(=O)O)OC
SMILES (Isomeric) COC1=CC(=C(C=C1)/C=C\C(=O)O)OC
InChI InChI=1S/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)10(7-9)15-2/h3-7H,1-2H3,(H,12,13)/b6-4-
InChI Key YIKHDPHTFYWYJV-XQRVVYSFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O4
Molecular Weight 208.21 g/mol
Exact Mass 208.07355886 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.80
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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AC-20488

2D Structure

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2D Structure of (Z)-3-(2,4-dimethoxyphenyl)prop-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.8887 88.87%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.8879 88.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9015 90.15%
OATP1B3 inhibitior + 0.9880 98.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8647 86.47%
P-glycoprotein inhibitior - 0.9799 97.99%
P-glycoprotein substrate - 0.9555 95.55%
CYP3A4 substrate - 0.6034 60.34%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.8567 85.67%
CYP3A4 inhibition - 0.8424 84.24%
CYP2C9 inhibition - 0.9552 95.52%
CYP2C19 inhibition - 0.7758 77.58%
CYP2D6 inhibition - 0.9626 96.26%
CYP1A2 inhibition - 0.8324 83.24%
CYP2C8 inhibition - 0.5791 57.91%
CYP inhibitory promiscuity - 0.7613 76.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6441 64.41%
Carcinogenicity (trinary) Non-required 0.6920 69.20%
Eye corrosion - 0.6345 63.45%
Eye irritation + 0.9606 96.06%
Skin irritation + 0.6266 62.66%
Skin corrosion - 0.9813 98.13%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7070 70.70%
Micronuclear + 0.5707 57.07%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8111 81.11%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6415 64.15%
Acute Oral Toxicity (c) II 0.5482 54.82%
Estrogen receptor binding - 0.6794 67.94%
Androgen receptor binding + 0.5642 56.42%
Thyroid receptor binding - 0.7767 77.67%
Glucocorticoid receptor binding - 0.7160 71.60%
Aromatase binding + 0.5615 56.15%
PPAR gamma - 0.6271 62.71%
Honey bee toxicity - 0.9613 96.13%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9717 97.17%

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 95.29% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.73% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.59% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.15% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.26% 96.09%
CHEMBL4208 P20618 Proteasome component C5 90.95% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.34% 99.17%
CHEMBL3714130 P46095 G-protein coupled receptor 6 88.27% 97.36%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.16% 95.50%

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.
Artemisia igniaria

Cross-Links

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PubChem 1622526
LOTUS LTS0086379
wikiData Q105348874