(3-hydroxyphenyl) (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

Details

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Internal ID 2e55d3a4-efe2-45e4-82a5-35630c361d99
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name (3-hydroxyphenyl) (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O6/c1-21-14-8-11(9-15(22-2)17(14)20)6-7-16(19)23-13-5-3-4-12(18)10-13/h3-10,18,20H,1-2H3/b7-6+
InChI Key WFGSIANPCBELDA-VOTSOKGWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O6
Molecular Weight 316.30 g/mol
Exact Mass 316.09468823 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3-hydroxyphenyl) (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 + 0.6904 69.04%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8145 81.45%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.9236 92.36%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7140 71.40%
P-glycoprotein inhibitior - 0.6196 61.96%
P-glycoprotein substrate - 0.8372 83.72%
CYP3A4 substrate + 0.5234 52.34%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.8380 83.80%
CYP3A4 inhibition - 0.7712 77.12%
CYP2C9 inhibition - 0.6398 63.98%
CYP2C19 inhibition + 0.5345 53.45%
CYP2D6 inhibition - 0.8938 89.38%
CYP1A2 inhibition + 0.5153 51.53%
CYP2C8 inhibition + 0.7214 72.14%
CYP inhibitory promiscuity + 0.5583 55.83%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7525 75.25%
Carcinogenicity (trinary) Non-required 0.6075 60.75%
Eye corrosion - 0.9727 97.27%
Eye irritation + 0.8093 80.93%
Skin irritation - 0.6523 65.23%
Skin corrosion - 0.9641 96.41%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6801 68.01%
Micronuclear + 0.7400 74.00%
Hepatotoxicity - 0.5476 54.76%
skin sensitisation - 0.8431 84.31%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6627 66.27%
Acute Oral Toxicity (c) III 0.5228 52.28%
Estrogen receptor binding + 0.9402 94.02%
Androgen receptor binding + 0.7354 73.54%
Thyroid receptor binding + 0.7172 71.72%
Glucocorticoid receptor binding + 0.7716 77.16%
Aromatase binding + 0.6391 63.91%
PPAR gamma + 0.7584 75.84%
Honey bee toxicity - 0.7644 76.44%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5745 57.45%
Fish aquatic toxicity + 0.9918 99.18%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.96% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.72% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.67% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.81% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.00% 96.09%
CHEMBL3194 P02766 Transthyretin 90.35% 90.71%
CHEMBL2581 P07339 Cathepsin D 89.33% 98.95%
CHEMBL2535 P11166 Glucose transporter 89.17% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 87.70% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.57% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.22% 89.00%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 83.71% 100.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.17% 91.07%

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.
Oxalis pes-caprae

Cross-Links

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PubChem 23656639
LOTUS LTS0101518
wikiData Q105303879