3,4,5-Trimethoxycinnamic acid, (Z)-

Details

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Internal ID efc23d29-de34-4e84-884f-6fe6a60a7c88
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name (Z)-3-(3,4,5-trimethoxyphenyl)prop-2-enoic acid
SMILES (Canonical) COC1=CC(=CC(=C1OC)OC)C=CC(=O)O
SMILES (Isomeric) COC1=CC(=CC(=C1OC)OC)/C=C\C(=O)O
InChI InChI=1S/C12H14O5/c1-15-9-6-8(4-5-11(13)14)7-10(16-2)12(9)17-3/h4-7H,1-3H3,(H,13,14)/b5-4-
InChI Key YTFVRYKNXDADBI-PLNGDYQASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H14O5
Molecular Weight 238.24 g/mol
Exact Mass 238.08412354 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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UNII-ZXP5LUI6QJ
3,4,5-Trimethoxycinnamic acid, (Z)-
Cinnamic acid, 3,4,5-trimethoxy-, (Z)-
(Z)-3,4,5-Trimethoxycinnamic acid
20329-99-1
2-Propenoic acid, 3-(3,4,5-trimethoxyphenyl)-, (Z)-
MEGxp0_001181
ACon1_001134
z-3,4,5-trimethoxycinnamic acid
NCGC00169644-01
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4,5-Trimethoxycinnamic acid, (Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9869 98.69%
Caco-2 + 0.8767 87.67%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.8067 80.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9525 95.25%
OATP1B3 inhibitior + 0.9672 96.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6949 69.49%
P-glycoprotein inhibitior - 0.9630 96.30%
P-glycoprotein substrate - 0.9778 97.78%
CYP3A4 substrate - 0.6681 66.81%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.8567 85.67%
CYP3A4 inhibition - 0.8462 84.62%
CYP2C9 inhibition - 0.9871 98.71%
CYP2C19 inhibition - 0.9155 91.55%
CYP2D6 inhibition - 0.9569 95.69%
CYP1A2 inhibition - 0.9299 92.99%
CYP2C8 inhibition + 0.5308 53.08%
CYP inhibitory promiscuity - 0.8290 82.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7340 73.40%
Carcinogenicity (trinary) Non-required 0.6140 61.40%
Eye corrosion - 0.7485 74.85%
Eye irritation + 0.9629 96.29%
Skin irritation - 0.5159 51.59%
Skin corrosion - 0.9806 98.06%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6541 65.41%
Micronuclear + 0.5507 55.07%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.8767 87.67%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.7170 71.70%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.6936 69.36%
Acute Oral Toxicity (c) II 0.4544 45.44%
Estrogen receptor binding + 0.6462 64.62%
Androgen receptor binding - 0.5402 54.02%
Thyroid receptor binding - 0.6085 60.85%
Glucocorticoid receptor binding - 0.8027 80.27%
Aromatase binding - 0.6025 60.25%
PPAR gamma - 0.7327 73.27%
Honey bee toxicity - 0.9052 90.52%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6055 60.55%
Fish aquatic toxicity + 0.9627 96.27%

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 95.15% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.26% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.02% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.61% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.06% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.89% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.64% 89.00%
CHEMBL3194 P02766 Transthyretin 80.10% 90.71%

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.
Descurainia sophia
Lepidium apetalum
Polygala sibirica
Polygala tenuifolia

Cross-Links

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PubChem 1715138
NPASS NPC108970