Octadeca-5,13-dienoic acid

Details

Top
Internal ID de8e191c-bb46-48fb-87c5-0be200c2a0b5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name octadeca-5,13-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h5-6,13-14H,2-4,7-12,15-17H2,1H3,(H,19,20)
InChI Key JBHNGBCIVVWDCA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H32O2
Molecular Weight 280.40 g/mol
Exact Mass 280.240230259 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.88
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Octadeca-5,13-dienoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.5569 55.69%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Plasma membrane 0.6181 61.81%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior - 0.3976 39.76%
OATP1B3 inhibitior - 0.4408 44.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6661 66.61%
P-glycoprotein inhibitior - 0.8664 86.64%
P-glycoprotein substrate - 0.9663 96.63%
CYP3A4 substrate - 0.6831 68.31%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9386 93.86%
CYP2C9 inhibition - 0.8711 87.11%
CYP2C19 inhibition - 0.9373 93.73%
CYP2D6 inhibition - 0.9519 95.19%
CYP1A2 inhibition + 0.8857 88.57%
CYP2C8 inhibition - 0.9406 94.06%
CYP inhibitory promiscuity - 0.9365 93.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6635 66.35%
Carcinogenicity (trinary) Non-required 0.7143 71.43%
Eye corrosion + 0.9709 97.09%
Eye irritation + 0.9711 97.11%
Skin irritation + 0.8485 84.85%
Skin corrosion + 0.7149 71.49%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3617 36.17%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7176 71.76%
skin sensitisation + 0.8470 84.70%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7915 79.15%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6609 66.09%
Acute Oral Toxicity (c) IV 0.7278 72.78%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.7828 78.28%
Thyroid receptor binding + 0.6097 60.97%
Glucocorticoid receptor binding - 0.5821 58.21%
Aromatase binding - 0.7895 78.95%
PPAR gamma + 0.8938 89.38%
Honey bee toxicity - 0.9956 99.56%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.9575 95.75%

Targets

Top

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 96.86% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.91% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 93.82% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.44% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.15% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 91.53% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.35% 96.95%
CHEMBL230 P35354 Cyclooxygenase-2 83.11% 89.63%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.34% 93.56%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 81.31% 96.00%

Plants that contains it

Top
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.
Leucosceptrum canum

Cross-Links

Top
PubChem 162953161
LOTUS LTS0033967
wikiData Q105124352