trans-Sinapate

Details

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Internal ID 3fa9f724-027d-40b5-a308-2dac08bf5cfb
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name 4-[(E)-2-carboxyethenyl]-2,6-dimethoxyphenolate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O5/c1-15-8-5-7(3-4-10(12)13)6-9(16-2)11(8)14/h3-6,14H,1-2H3,(H,12,13)/p-1/b4-3+
InChI Key PCMORTLOPMLEFB-ONEGZZNKSA-M
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C11H11O5-
Molecular Weight 223.20 g/mol
Exact Mass 223.06064845 g/mol
Topological Polar Surface Area (TPSA) 78.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 0.88
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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3,5-dimethoxy-4-hydroxycinnamate
E-sinapate
AC1NUT1R
CHEBI:30023
4-hydroxy-3,5-dimethoxycinnamate
(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate
Q27104099
(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate

2D Structure

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2D Structure of trans-Sinapate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9497 94.97%
Caco-2 + 0.5291 52.91%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7726 77.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9195 91.95%
OATP1B3 inhibitior + 0.9783 97.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7876 78.76%
P-glycoprotein inhibitior - 0.9628 96.28%
P-glycoprotein substrate - 0.9531 95.31%
CYP3A4 substrate - 0.6778 67.78%
CYP2C9 substrate - 0.6017 60.17%
CYP2D6 substrate - 0.8667 86.67%
CYP3A4 inhibition - 0.8868 88.68%
CYP2C9 inhibition - 0.9625 96.25%
CYP2C19 inhibition - 0.8296 82.96%
CYP2D6 inhibition - 0.9402 94.02%
CYP1A2 inhibition - 0.8849 88.49%
CYP2C8 inhibition - 0.7096 70.96%
CYP inhibitory promiscuity - 0.8516 85.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7180 71.80%
Carcinogenicity (trinary) Non-required 0.6538 65.38%
Eye corrosion - 0.6847 68.47%
Eye irritation + 0.9862 98.62%
Skin irritation + 0.6290 62.90%
Skin corrosion - 0.9668 96.68%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8521 85.21%
Micronuclear + 0.6407 64.07%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8227 82.27%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.6577 65.77%
Acute Oral Toxicity (c) III 0.4582 45.82%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.5248 52.48%
Thyroid receptor binding - 0.5940 59.40%
Glucocorticoid receptor binding - 0.7463 74.63%
Aromatase binding - 0.8089 80.89%
PPAR gamma - 0.6295 62.95%
Honey bee toxicity - 0.9293 92.93%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6055 60.55%
Fish aquatic toxicity + 0.9595 95.95%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.62% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.18% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.95% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.82% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 86.09% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.92% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.34% 99.17%
CHEMBL3194 P02766 Transthyretin 82.49% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.19% 96.95%

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.
Brassica oleracea
Glycyrrhiza uralensis
Juglans nigra
Magnolia officinalis

Cross-Links

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PubChem 54710960
NPASS NPC300323