18-Hydroxyoctadec-9-enoic acid

Details

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Internal ID 7e10cc1e-693c-4490-a450-330df62718b0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (E)-18-hydroxyoctadec-9-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H34O3/c19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18(20)21/h1-2,19H,3-17H2,(H,20,21)/b2-1+
InChI Key LQUHZVLTTWMBTO-OWOJBTEDSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C18H34O3
Molecular Weight 298.50 g/mol
Exact Mass 298.25079494 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.08
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 16

Synonyms

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(E)-18-hydroxyoctadec-9-enoic acid
RefChem:1057660
18-Hydroxy-9-octadecenoic acid
3329-38-2
9-Octadecenoic acid, 18-hydroxy-
SCHEMBL561758
18-hydroxyoctadec-9-enoicacid

2D Structure

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2D Structure of 18-Hydroxyoctadec-9-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9580 95.80%
Caco-2 - 0.6193 61.93%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8064 80.64%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.8140 81.40%
OATP1B3 inhibitior + 0.9325 93.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6721 67.21%
P-glycoprotein inhibitior - 0.8495 84.95%
P-glycoprotein substrate - 0.9836 98.36%
CYP3A4 substrate - 0.6925 69.25%
CYP2C9 substrate + 0.5995 59.95%
CYP2D6 substrate - 0.8503 85.03%
CYP3A4 inhibition - 0.9228 92.28%
CYP2C9 inhibition - 0.9109 91.09%
CYP2C19 inhibition - 0.9524 95.24%
CYP2D6 inhibition - 0.9623 96.23%
CYP1A2 inhibition - 0.8724 87.24%
CYP2C8 inhibition - 0.9518 95.18%
CYP inhibitory promiscuity - 0.9608 96.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.7168 71.68%
Eye corrosion + 0.7220 72.20%
Eye irritation + 0.9520 95.20%
Skin irritation - 0.7031 70.31%
Skin corrosion - 0.9077 90.77%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7850 78.50%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.8135 81.35%
skin sensitisation - 0.8665 86.65%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.7064 70.64%
Acute Oral Toxicity (c) III 0.7474 74.74%
Estrogen receptor binding - 0.5824 58.24%
Androgen receptor binding - 0.8205 82.05%
Thyroid receptor binding + 0.5801 58.01%
Glucocorticoid receptor binding - 0.6666 66.66%
Aromatase binding - 0.6922 69.22%
PPAR gamma + 0.8490 84.90%
Honey bee toxicity - 0.9764 97.64%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.6213 62.13%
Fish aquatic toxicity - 0.3957 39.57%

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 96.84% 99.17%
CHEMBL1781 P11387 DNA topoisomerase I 91.59% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.38% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.46% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.83% 98.95%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 83.55% 92.26%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.83% 96.95%
CHEMBL1829 O15379 Histone deacetylase 3 80.46% 95.00%

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.
Pinus radiata

Cross-Links

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PubChem 6365155
LOTUS LTS0253224
wikiData Q105155825