methyl (Z)-2-hydroxy-3-(4-hydroxyphenyl)prop-2-enoate

Details

Top
Internal ID c6172752-5d8f-4a3a-b405-db75d1771ff3
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acid esters > Coumaric acid esters
IUPAC Name methyl (Z)-2-hydroxy-3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H10O4/c1-14-10(13)9(12)6-7-2-4-8(11)5-3-7/h2-6,11-12H,1H3/b9-6-
InChI Key QCZFQWATVFWNJO-TWGQIWQCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H10O4
Molecular Weight 194.18 g/mol
Exact Mass 194.05790880 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.46
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of methyl (Z)-2-hydroxy-3-(4-hydroxyphenyl)prop-2-enoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9869 98.69%
Caco-2 + 0.7253 72.53%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8477 84.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9208 92.08%
OATP1B3 inhibitior + 0.9583 95.83%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6958 69.58%
P-glycoprotein inhibitior - 0.9835 98.35%
P-glycoprotein substrate - 0.9508 95.08%
CYP3A4 substrate - 0.6413 64.13%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.9241 92.41%
CYP2C9 inhibition - 0.7484 74.84%
CYP2C19 inhibition - 0.7684 76.84%
CYP2D6 inhibition - 0.9634 96.34%
CYP1A2 inhibition - 0.7115 71.15%
CYP2C8 inhibition - 0.7060 70.60%
CYP inhibitory promiscuity - 0.8011 80.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6370 63.70%
Carcinogenicity (trinary) Non-required 0.4791 47.91%
Eye corrosion - 0.7935 79.35%
Eye irritation + 0.9937 99.37%
Skin irritation + 0.5422 54.22%
Skin corrosion - 0.9423 94.23%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7276 72.76%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5014 50.14%
skin sensitisation - 0.7413 74.13%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6903 69.03%
Acute Oral Toxicity (c) IV 0.5073 50.73%
Estrogen receptor binding - 0.5979 59.79%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.7849 78.49%
Glucocorticoid receptor binding - 0.8101 81.01%
Aromatase binding - 0.6839 68.39%
PPAR gamma - 0.8052 80.52%
Honey bee toxicity - 0.9235 92.35%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9225 92.25%

Targets

Top

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 94.13% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.30% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.73% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.46% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.41% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.34% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.98% 94.73%
CHEMBL4208 P20618 Proteasome component C5 81.27% 90.00%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 15834376
LOTUS LTS0197215
wikiData Q104667996