3-Ethenylnonanoic acid

Details

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Internal ID b64950e3-714f-491e-9ba4-4d7f55e31121
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 3-ethenylnonanoic acid
SMILES (Canonical) CCCCCCC(CC(=O)O)C=C
SMILES (Isomeric) CCCCCCC(CC(=O)O)C=C
InChI InChI=1S/C11H20O2/c1-3-5-6-7-8-10(4-2)9-11(12)13/h4,10H,2-3,5-9H2,1H3,(H,12,13)
InChI Key CUSNFCKBWYVYMM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O2
Molecular Weight 184.27 g/mol
Exact Mass 184.146329876 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Ethenylnonanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.7972 79.72%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Plasma membrane 0.6065 60.65%
OATP2B1 inhibitior - 0.8485 84.85%
OATP1B1 inhibitior + 0.9276 92.76%
OATP1B3 inhibitior - 0.3736 37.36%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8434 84.34%
P-glycoprotein inhibitior - 0.9814 98.14%
P-glycoprotein substrate - 0.9379 93.79%
CYP3A4 substrate - 0.5909 59.09%
CYP2C9 substrate + 0.6882 68.82%
CYP2D6 substrate - 0.8899 88.99%
CYP3A4 inhibition - 0.8958 89.58%
CYP2C9 inhibition - 0.9088 90.88%
CYP2C19 inhibition - 0.9378 93.78%
CYP2D6 inhibition - 0.9516 95.16%
CYP1A2 inhibition + 0.7878 78.78%
CYP2C8 inhibition - 0.9411 94.11%
CYP inhibitory promiscuity - 0.9414 94.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6735 67.35%
Carcinogenicity (trinary) Non-required 0.7378 73.78%
Eye corrosion + 0.9650 96.50%
Eye irritation + 0.9576 95.76%
Skin irritation + 0.8884 88.84%
Skin corrosion - 0.5358 53.58%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5591 55.91%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7052 70.52%
skin sensitisation + 0.8847 88.47%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8591 85.91%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.4753 47.53%
Acute Oral Toxicity (c) IV 0.5027 50.27%
Estrogen receptor binding - 0.8132 81.32%
Androgen receptor binding - 0.8029 80.29%
Thyroid receptor binding - 0.7604 76.04%
Glucocorticoid receptor binding - 0.6213 62.13%
Aromatase binding - 0.7448 74.48%
PPAR gamma - 0.6963 69.63%
Honey bee toxicity - 0.9657 96.57%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6251 62.51%
Fish aquatic toxicity + 0.9795 97.95%

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
CHEMBL2581 P07339 Cathepsin D 95.88% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.44% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.02% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.01% 85.94%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.06% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.88% 93.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.13% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 87.30% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 86.83% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.30% 92.86%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.65% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.49% 91.19%
CHEMBL3776 Q14790 Caspase-8 82.01% 97.06%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.95% 96.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.90% 91.81%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.88% 96.47%
CHEMBL3401 O75469 Pregnane X receptor 81.73% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 80.69% 93.31%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.51% 100.00%

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.
Croton eluteria

Cross-Links

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PubChem 53741265
LOTUS LTS0115291
wikiData Q104970459