18-Fluorooleic acid

Details

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Internal ID 7eb063d0-981f-45b9-8069-2111f3f2713b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (Z)-18-fluorooctadec-9-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H33FO2/c19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18(20)21/h1-2H,3-17H2,(H,20,21)/b2-1-
InChI Key XZCKFYWUUUBKNC-UPHRSURJSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C18H33FO2
Molecular Weight 300.50 g/mol
Exact Mass 300.24645845 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.70
Atomic LogP (AlogP) 6.06
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 16

Synonyms

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Oleic acid, 18-fluoro-
18-Fluorooleic acid
18-fluoro-9Z-octadecenoic acid
9-Octadecenoic acid, 18-fluoro-, (Z)-
Z49M478WU7
J1.240.568E
18-fluoro-oleic acid
RefChem:1057655
Fluoro-oleic acid
1478-37-1
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 18-Fluorooleic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 - 0.5679 56.79%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6802 68.02%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8558 85.58%
OATP1B3 inhibitior + 0.8973 89.73%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5666 56.66%
P-glycoprotein inhibitior - 0.8204 82.04%
P-glycoprotein substrate - 0.9713 97.13%
CYP3A4 substrate - 0.6809 68.09%
CYP2C9 substrate + 0.6171 61.71%
CYP2D6 substrate - 0.8443 84.43%
CYP3A4 inhibition - 0.9163 91.63%
CYP2C9 inhibition - 0.8673 86.73%
CYP2C19 inhibition - 0.9461 94.61%
CYP2D6 inhibition - 0.9529 95.29%
CYP1A2 inhibition - 0.6807 68.07%
CYP2C8 inhibition - 0.9386 93.86%
CYP inhibitory promiscuity - 0.9788 97.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6391 63.91%
Carcinogenicity (trinary) Non-required 0.5712 57.12%
Eye corrosion + 0.9499 94.99%
Eye irritation + 0.9217 92.17%
Skin irritation + 0.6502 65.02%
Skin corrosion - 0.7466 74.66%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8021 80.21%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation + 0.7397 73.97%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity - 0.7293 72.93%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7577 75.77%
Acute Oral Toxicity (c) III 0.7447 74.47%
Estrogen receptor binding - 0.5543 55.43%
Androgen receptor binding - 0.8934 89.34%
Thyroid receptor binding + 0.5743 57.43%
Glucocorticoid receptor binding - 0.7967 79.67%
Aromatase binding - 0.6281 62.81%
PPAR gamma + 0.8292 82.92%
Honey bee toxicity - 0.9701 97.01%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.7629 76.29%

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 96.61% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.06% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 89.49% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.04% 90.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 84.36% 92.26%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.06% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.24% 96.95%
CHEMBL2581 P07339 Cathepsin D 80.66% 98.95%
CHEMBL1829 O15379 Histone deacetylase 3 80.30% 95.00%

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 5312955
LOTUS LTS0000075
wikiData Q27294979