(9R,12Z,15Z)-9-hydroxyoctadeca-12,15-dienoic acid

Details

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Internal ID f548cfef-08e6-4d43-afc7-a683c821f3a0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name (9R,12Z,15Z)-9-hydroxyoctadeca-12,15-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H32O3/c1-2-3-4-5-6-8-11-14-17(19)15-12-9-7-10-13-16-18(20)21/h3-4,6,8,17,19H,2,5,7,9-16H2,1H3,(H,20,21)/b4-3-,8-6-/t17-/m0/s1
InChI Key XARXRMIAOTVTEH-NUSIUILESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H32O3
Molecular Weight 296.40 g/mol
Exact Mass 296.23514488 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.86
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (9R,12Z,15Z)-9-hydroxyoctadeca-12,15-dienoic 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 - 0.5979 59.79%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7106 71.06%
OATP2B1 inhibitior - 0.8510 85.10%
OATP1B1 inhibitior + 0.7527 75.27%
OATP1B3 inhibitior + 0.8868 88.68%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5917 59.17%
P-glycoprotein inhibitior - 0.8570 85.70%
P-glycoprotein substrate - 0.8583 85.83%
CYP3A4 substrate - 0.5740 57.40%
CYP2C9 substrate + 0.6045 60.45%
CYP2D6 substrate - 0.8576 85.76%
CYP3A4 inhibition - 0.9305 93.05%
CYP2C9 inhibition - 0.9122 91.22%
CYP2C19 inhibition - 0.9474 94.74%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition - 0.6483 64.83%
CYP2C8 inhibition - 0.9391 93.91%
CYP inhibitory promiscuity - 0.9144 91.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7635 76.35%
Carcinogenicity (trinary) Non-required 0.6666 66.66%
Eye corrosion + 0.5000 50.00%
Eye irritation - 0.6389 63.89%
Skin irritation - 0.5965 59.65%
Skin corrosion - 0.7641 76.41%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3946 39.46%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6699 66.99%
skin sensitisation + 0.4909 49.09%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity - 0.7228 72.28%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8443 84.43%
Acute Oral Toxicity (c) IV 0.6007 60.07%
Estrogen receptor binding + 0.7065 70.65%
Androgen receptor binding - 0.8712 87.12%
Thyroid receptor binding + 0.5617 56.17%
Glucocorticoid receptor binding - 0.6866 68.66%
Aromatase binding - 0.5376 53.76%
PPAR gamma + 0.9007 90.07%
Honey bee toxicity - 0.9790 97.90%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.7906 79.06%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.07% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.49% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.41% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 93.43% 83.82%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 85.30% 92.26%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.14% 93.56%
CHEMBL1781 P11387 DNA topoisomerase I 85.12% 97.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.00% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.02% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.10% 96.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.52% 97.29%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.47% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163048913
LOTUS LTS0157196
wikiData Q105324084