Tetracosyl (z)-p-coumarate

Details

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Internal ID c5ff18c0-b87f-437a-bfa4-53f485e284f5
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acid esters > Coumaric acid esters
IUPAC Name tetracosyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)/C=C\C1=CC=C(C=C1)O
InChI InChI=1S/C33H56O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-30-36-33(35)29-26-31-24-27-32(34)28-25-31/h24-29,34H,2-23,30H2,1H3/b29-26-
InChI Key FNUQVBAOIKMXFM-WCTVFOPTSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C33H56O3
Molecular Weight 500.80 g/mol
Exact Mass 500.42294564 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 13.90
Atomic LogP (AlogP) 10.55
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 25

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tetracosyl (z)-p-coumarate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.7252 72.52%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.9000 90.00%
Subcellular localzation Mitochondria 0.6896 68.96%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.8881 88.81%
OATP1B3 inhibitior + 0.9282 92.82%
MATE1 inhibitior - 0.5600 56.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8583 85.83%
P-glycoprotein inhibitior - 0.5326 53.26%
P-glycoprotein substrate - 0.8871 88.71%
CYP3A4 substrate - 0.5244 52.44%
CYP2C9 substrate + 0.5976 59.76%
CYP2D6 substrate - 0.8619 86.19%
CYP3A4 inhibition - 0.7322 73.22%
CYP2C9 inhibition - 0.8905 89.05%
CYP2C19 inhibition + 0.6531 65.31%
CYP2D6 inhibition - 0.8436 84.36%
CYP1A2 inhibition + 0.7271 72.71%
CYP2C8 inhibition + 0.7688 76.88%
CYP inhibitory promiscuity - 0.7184 71.84%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8023 80.23%
Carcinogenicity (trinary) Non-required 0.6570 65.70%
Eye corrosion - 0.9661 96.61%
Eye irritation - 0.5236 52.36%
Skin irritation - 0.7872 78.72%
Skin corrosion - 0.9847 98.47%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3679 36.79%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation + 0.4849 48.49%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.8179 81.79%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5189 51.89%
Acute Oral Toxicity (c) III 0.6434 64.34%
Estrogen receptor binding + 0.7205 72.05%
Androgen receptor binding + 0.8467 84.67%
Thyroid receptor binding - 0.5889 58.89%
Glucocorticoid receptor binding - 0.5671 56.71%
Aromatase binding - 0.5869 58.69%
PPAR gamma + 0.5409 54.09%
Honey bee toxicity - 0.9832 98.32%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7187 71.87%
Fish aquatic toxicity + 0.9948 99.48%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.41% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.32% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.76% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.52% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 90.97% 98.35%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.38% 96.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.38% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.07% 91.11%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.91% 91.71%
CHEMBL3194 P02766 Transthyretin 88.91% 90.71%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.85% 97.29%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.74% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.64% 94.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.27% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.70% 93.56%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.39% 80.78%
CHEMBL3401 O75469 Pregnane X receptor 80.26% 94.73%

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.
Artemisia igniaria
Dendrobium falconeri

Cross-Links

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PubChem 42642799
LOTUS LTS0001722
wikiData Q104998543