(Z)-3-(3-methoxy-2-methoxycarbonyl-5-methylphenyl)prop-2-enoic acid

Details

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Internal ID a0fc964f-d91f-4804-a8da-782bcd3d340b
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name (Z)-3-(3-methoxy-2-methoxycarbonyl-5-methylphenyl)prop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O5/c1-8-6-9(4-5-11(14)15)12(13(16)18-3)10(7-8)17-2/h4-7H,1-3H3,(H,14,15)/b5-4-
InChI Key ATJFASRWRPLFTM-PLNGDYQASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O5
Molecular Weight 250.25 g/mol
Exact Mass 250.08412354 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-3-(3-methoxy-2-methoxycarbonyl-5-methylphenyl)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 + 0.9865 98.65%
Caco-2 + 0.7367 73.67%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8799 87.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8717 87.17%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7561 75.61%
P-glycoprotein inhibitior - 0.9381 93.81%
P-glycoprotein substrate - 0.9000 90.00%
CYP3A4 substrate - 0.5471 54.71%
CYP2C9 substrate + 0.6079 60.79%
CYP2D6 substrate - 0.8983 89.83%
CYP3A4 inhibition - 0.8563 85.63%
CYP2C9 inhibition - 0.9718 97.18%
CYP2C19 inhibition - 0.9469 94.69%
CYP2D6 inhibition - 0.9353 93.53%
CYP1A2 inhibition - 0.8750 87.50%
CYP2C8 inhibition + 0.5252 52.52%
CYP inhibitory promiscuity - 0.8969 89.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6476 64.76%
Carcinogenicity (trinary) Non-required 0.6512 65.12%
Eye corrosion - 0.8641 86.41%
Eye irritation + 0.8300 83.00%
Skin irritation - 0.6276 62.76%
Skin corrosion - 0.9680 96.80%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7289 72.89%
Micronuclear + 0.6007 60.07%
Hepatotoxicity + 0.6302 63.02%
skin sensitisation - 0.8965 89.65%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.7281 72.81%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5222 52.22%
Acute Oral Toxicity (c) II 0.7088 70.88%
Estrogen receptor binding - 0.4839 48.39%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.7154 71.54%
Glucocorticoid receptor binding - 0.6307 63.07%
Aromatase binding - 0.5165 51.65%
PPAR gamma - 0.5843 58.43%
Honey bee toxicity - 0.9353 93.53%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9823 98.23%

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 91.71% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.66% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.11% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.96% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.91% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.14% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.64% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 84.83% 91.19%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.75% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.74% 94.73%

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.
Diospyros celebica

Cross-Links

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PubChem 14539515
LOTUS LTS0227868
wikiData Q104918452