cis-Sinapic acid

Details

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Internal ID 2e65e088-35cd-42d2-9e97-f5b623035e42
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acids
IUPAC Name (Z)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoic acid
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C=CC(=O)O
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)/C=C\C(=O)O
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)/b4-3-
InChI Key PCMORTLOPMLEFB-ARJAWSKDSA-N
Popularity 363 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O5
Molecular Weight 224.21 g/mol
Exact Mass 224.06847348 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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Z-Sinapinic acid
cis-Sinapinic acid
Sinapic acid, (Z)-
UNII-64J2B0K41V
7361-90-2
64J2B0K41V
Cinnamic acid, 4-hydroxy-3,5-dimethoxy-, (Z)-
2-Propenoic acid, 3-(4-hydroxy-3,5-dimethoxyphenyl)-, (Z)-
2-Propenoic acid, 3-(4-hydroxy-3,5-dimethoxyphenyl)-, (2Z)-
EINECS 208-487-3
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-Sinapic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9801 98.01%
Caco-2 + 0.5291 52.91%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8118 81.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8888 88.88%
OATP1B3 inhibitior + 0.9763 97.63%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7876 78.76%
P-glycoprotein inhibitior - 0.9628 96.28%
P-glycoprotein substrate - 0.9400 94.00%
CYP3A4 substrate - 0.6637 66.37%
CYP2C9 substrate - 0.6110 61.10%
CYP2D6 substrate - 0.8502 85.02%
CYP3A4 inhibition - 0.8748 87.48%
CYP2C9 inhibition - 0.8380 83.80%
CYP2C19 inhibition - 0.7182 71.82%
CYP2D6 inhibition - 0.9297 92.97%
CYP1A2 inhibition - 0.8445 84.45%
CYP2C8 inhibition + 0.4554 45.54%
CYP inhibitory promiscuity - 0.7608 76.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7180 71.80%
Carcinogenicity (trinary) Non-required 0.6699 66.99%
Eye corrosion - 0.6968 69.68%
Eye irritation + 0.9862 98.62%
Skin irritation + 0.6304 63.04%
Skin corrosion - 0.9403 94.03%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8521 85.21%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.7259 72.59%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.7347 73.47%
Acute Oral Toxicity (c) III 0.4500 45.00%
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 - 0.9305 93.05%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6155 61.55%
Fish aquatic toxicity + 0.9626 96.26%

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 95.48% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.41% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.45% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.40% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.09% 96.09%
CHEMBL3194 P02766 Transthyretin 89.05% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.85% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.24% 99.17%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 80.54% 98.21%

Cross-Links

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PubChem 1549091
NPASS NPC119090
LOTUS LTS0163988
wikiData Q27145906