(10E,12E,14R)-14-hydroxy-9-oxooctadeca-10,12-dienoic acid

Details

Top
Internal ID 8380c1aa-cdbb-43c6-a585-3a6441ae6b78
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name (10E,12E,14R)-14-hydroxy-9-oxooctadeca-10,12-dienoic acid
SMILES (Canonical) CCCCC(C=CC=CC(=O)CCCCCCCC(=O)O)O
SMILES (Isomeric) CCCC[C@H](/C=C/C=C/C(=O)CCCCCCCC(=O)O)O
InChI InChI=1S/C18H30O4/c1-2-3-11-16(19)13-9-10-14-17(20)12-7-5-4-6-8-15-18(21)22/h9-10,13-14,16,19H,2-8,11-12,15H2,1H3,(H,21,22)/b13-9+,14-10+/t16-/m1/s1
InChI Key GDCBVHSUEZTUIW-BRKJJSFFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H30O4
Molecular Weight 310.40 g/mol
Exact Mass 310.21440943 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.03
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (10E,12E,14R)-14-hydroxy-9-oxooctadeca-10,12-dienoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9455 94.55%
Caco-2 - 0.6645 66.45%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.8080 80.80%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.8999 89.99%
OATP1B3 inhibitior + 0.9285 92.85%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7134 71.34%
P-glycoprotein inhibitior - 0.8232 82.32%
P-glycoprotein substrate - 0.8887 88.87%
CYP3A4 substrate - 0.5626 56.26%
CYP2C9 substrate - 0.5973 59.73%
CYP2D6 substrate - 0.8947 89.47%
CYP3A4 inhibition - 0.8728 87.28%
CYP2C9 inhibition - 0.9262 92.62%
CYP2C19 inhibition - 0.9345 93.45%
CYP2D6 inhibition - 0.9394 93.94%
CYP1A2 inhibition - 0.5426 54.26%
CYP2C8 inhibition - 0.9033 90.33%
CYP inhibitory promiscuity - 0.9606 96.06%
UGT catelyzed - 0.6638 66.38%
Carcinogenicity (binary) - 0.7935 79.35%
Carcinogenicity (trinary) Non-required 0.7675 76.75%
Eye corrosion - 0.6347 63.47%
Eye irritation - 0.6381 63.81%
Skin irritation - 0.6798 67.98%
Skin corrosion - 0.8662 86.62%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5071 50.71%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5821 58.21%
skin sensitisation - 0.8131 81.31%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.9024 90.24%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7174 71.74%
Acute Oral Toxicity (c) III 0.6047 60.47%
Estrogen receptor binding - 0.4847 48.47%
Androgen receptor binding - 0.8232 82.32%
Thyroid receptor binding + 0.5597 55.97%
Glucocorticoid receptor binding + 0.5866 58.66%
Aromatase binding - 0.6540 65.40%
PPAR gamma + 0.6571 65.71%
Honey bee toxicity - 0.9775 97.75%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9743 97.43%

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
CHEMBL2581 P07339 Cathepsin D 97.54% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 97.48% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.06% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.69% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.75% 90.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.35% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.28% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.40% 91.11%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 86.87% 96.00%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 86.00% 97.34%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.97% 91.81%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 84.46% 92.26%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.43% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.08% 93.56%
CHEMBL1907 P15144 Aminopeptidase N 83.76% 93.31%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 83.61% 92.29%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.16% 96.47%
CHEMBL1781 P11387 DNA topoisomerase I 81.06% 97.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.96% 91.19%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.80% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 80.64% 83.82%

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.
Melia azedarach

Cross-Links

Top
PubChem 102256999
LOTUS LTS0251171
wikiData Q105006651