2-O-Coumaroylglycerol

Details

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Internal ID d5dd8747-bacb-4da0-b1d9-068f7afded9d
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acid esters > Coumaric acid esters
IUPAC Name 1,3-dihydroxypropan-2-yl (E)-3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical) C1=CC(=CC=C1C=CC(=O)OC(CO)CO)O
SMILES (Isomeric) C1=CC(=CC=C1/C=C/C(=O)OC(CO)CO)O
InChI InChI=1S/C12H14O5/c13-7-11(8-14)17-12(16)6-3-9-1-4-10(15)5-2-9/h1-6,11,13-15H,7-8H2/b6-3+
InChI Key FFUFAQREPMLRLE-ZZXKWVIFSA-N
Popularity 2 references 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) 87.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.30
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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SCHEMBL20371008

2D Structure

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2D Structure of 2-O-Coumaroylglycerol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9188 91.88%
Caco-2 + 0.6796 67.96%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.7600 76.00%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.9161 91.61%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9338 93.38%
BSEP inhibitior - 0.9115 91.15%
P-glycoprotein inhibitior - 0.9694 96.94%
P-glycoprotein substrate - 0.9470 94.70%
CYP3A4 substrate - 0.6077 60.77%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8578 85.78%
CYP3A4 inhibition - 0.8733 87.33%
CYP2C9 inhibition - 0.9310 93.10%
CYP2C19 inhibition - 0.8961 89.61%
CYP2D6 inhibition - 0.9525 95.25%
CYP1A2 inhibition - 0.8599 85.99%
CYP2C8 inhibition + 0.4725 47.25%
CYP inhibitory promiscuity - 0.8265 82.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8550 85.50%
Carcinogenicity (trinary) Non-required 0.6760 67.60%
Eye corrosion - 0.9829 98.29%
Eye irritation + 0.9008 90.08%
Skin irritation - 0.6569 65.69%
Skin corrosion - 0.9703 97.03%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7441 74.41%
Micronuclear - 0.6685 66.85%
Hepatotoxicity - 0.8091 80.91%
skin sensitisation + 0.5063 50.63%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5761 57.61%
Acute Oral Toxicity (c) III 0.6727 67.27%
Estrogen receptor binding - 0.6939 69.39%
Androgen receptor binding + 0.6444 64.44%
Thyroid receptor binding - 0.7029 70.29%
Glucocorticoid receptor binding - 0.5941 59.41%
Aromatase binding - 0.5388 53.88%
PPAR gamma + 0.5197 51.97%
Honey bee toxicity - 0.8069 80.69%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6655 66.55%
Fish aquatic toxicity + 0.7140 71.40%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.96% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.23% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.01% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.92% 96.00%
CHEMBL3194 P02766 Transthyretin 88.23% 90.71%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 87.64% 89.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.62% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.58% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.68% 91.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.45% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.48% 98.95%

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.
Juncus effusus
Smilax perfoliata

Cross-Links

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PubChem 101688442
LOTUS LTS0150687
wikiData Q104398918