(8R,11E)-8-hydroxyoctadeca-11,17-dien-9-ynoic acid

Details

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Internal ID 337c7fb1-ceac-4a51-812c-700fc6e76a53
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (8R,11E)-8-hydroxyoctadeca-11,17-dien-9-ynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H28O3/c1-2-3-4-5-6-7-8-11-14-17(19)15-12-9-10-13-16-18(20)21/h2,7-8,17,19H,1,3-6,9-10,12-13,15-16H2,(H,20,21)/b8-7+/t17-/m0/s1
InChI Key KICRKYKTMPUVKC-OZSKJFCKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H28O3
Molecular Weight 292.40 g/mol
Exact Mass 292.20384475 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.08
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8R,11E)-8-hydroxyoctadeca-11,17-dien-9-ynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9409 94.09%
Caco-2 - 0.7338 73.38%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7572 75.72%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.8667 86.67%
OATP1B3 inhibitior + 0.9329 93.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5357 53.57%
P-glycoprotein inhibitior - 0.8364 83.64%
P-glycoprotein substrate - 0.8826 88.26%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7914 79.14%
CYP2D6 substrate - 0.8447 84.47%
CYP3A4 inhibition - 0.8186 81.86%
CYP2C9 inhibition - 0.8081 80.81%
CYP2C19 inhibition - 0.8936 89.36%
CYP2D6 inhibition - 0.9572 95.72%
CYP1A2 inhibition - 0.7272 72.72%
CYP2C8 inhibition - 0.8148 81.48%
CYP inhibitory promiscuity - 0.9234 92.34%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7135 71.35%
Carcinogenicity (trinary) Non-required 0.6910 69.10%
Eye corrosion + 0.7116 71.16%
Eye irritation - 0.9036 90.36%
Skin irritation - 0.6048 60.48%
Skin corrosion - 0.7080 70.80%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8054 80.54%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.9217 92.17%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7142 71.42%
Acute Oral Toxicity (c) III 0.5906 59.06%
Estrogen receptor binding + 0.6124 61.24%
Androgen receptor binding - 0.7542 75.42%
Thyroid receptor binding + 0.7244 72.44%
Glucocorticoid receptor binding + 0.5543 55.43%
Aromatase binding - 0.5275 52.75%
PPAR gamma + 0.7909 79.09%
Honey bee toxicity - 0.8560 85.60%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.8565 85.65%

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 97.58% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.07% 91.11%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 92.01% 97.34%
CHEMBL2581 P07339 Cathepsin D 91.70% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.42% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 89.28% 97.00%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 88.88% 91.67%
CHEMBL221 P23219 Cyclooxygenase-1 88.74% 90.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 87.78% 92.26%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.60% 95.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.90% 92.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.49% 85.94%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.11% 93.56%
CHEMBL3629 P68400 Casein kinase II alpha 83.83% 98.89%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.27% 97.29%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.10% 96.47%
CHEMBL340 P08684 Cytochrome P450 3A4 82.81% 91.19%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.44% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.36% 97.21%
CHEMBL236 P41143 Delta opioid receptor 82.29% 99.35%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.29% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.12% 96.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.27% 89.34%

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.
Jodina rhombifolia

Cross-Links

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PubChem 163042243
LOTUS LTS0152246
wikiData Q105141446