3,13-Octadecadien-1-ol, (E,E)-

Details

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Internal ID 00d8ef22-bfde-4c85-84cf-17f1025c528c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name octadeca-3,13-dien-1-ol
SMILES (Canonical) CCCCC=CCCCCCCCCC=CCCO
SMILES (Isomeric) CCCCC=CCCCCCCCCC=CCCO
InChI InChI=1S/C18H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h5-6,15-16,19H,2-4,7-14,17-18H2,1H3
InChI Key QBNCGBJHGBGHLS-UHFFFAOYSA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C18H34O
Molecular Weight 266.50 g/mol
Exact Mass 266.260965704 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.90
Atomic LogP (AlogP) 5.79
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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3,13-Octadecadien-1-ol, (E,E)-
3,13-octadecadien-1-ol
octadeca-3,13-dien-1-ol

2D Structure

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2D Structure of 3,13-Octadecadien-1-ol, (E,E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.7580 75.80%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Lysosomes 0.5290 52.90%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.8034 80.34%
OATP1B3 inhibitior + 0.9073 90.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5369 53.69%
P-glycoprotein inhibitior - 0.8896 88.96%
P-glycoprotein substrate - 0.9378 93.78%
CYP3A4 substrate - 0.6951 69.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9320 93.20%
CYP2C9 inhibition - 0.9207 92.07%
CYP2C19 inhibition - 0.9196 91.96%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.5408 54.08%
CYP2C8 inhibition - 0.9448 94.48%
CYP inhibitory promiscuity - 0.8613 86.13%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.7440 74.40%
Eye corrosion + 0.9077 90.77%
Eye irritation + 0.8922 89.22%
Skin irritation + 0.8762 87.62%
Skin corrosion - 0.9602 96.02%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3872 38.72%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5473 54.73%
skin sensitisation + 0.8327 83.27%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5657 56.57%
Acute Oral Toxicity (c) III 0.7997 79.97%
Estrogen receptor binding - 0.5977 59.77%
Androgen receptor binding - 0.7980 79.80%
Thyroid receptor binding + 0.6354 63.54%
Glucocorticoid receptor binding - 0.6693 66.93%
Aromatase binding - 0.5933 59.33%
PPAR gamma + 0.7966 79.66%
Honey bee toxicity - 0.9934 99.34%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5286 52.86%
Fish aquatic toxicity + 0.7431 74.31%

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 93.79% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.92% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 91.43% 87.45%
CHEMBL2581 P07339 Cathepsin D 91.24% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.51% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.99% 92.86%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.32% 96.09%
CHEMBL2664 P23526 Adenosylhomocysteinase 84.42% 86.67%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.48% 91.81%
CHEMBL1781 P11387 DNA topoisomerase I 82.11% 97.00%
CHEMBL299 P17252 Protein kinase C alpha 80.39% 98.03%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.30% 96.95%
CHEMBL1907 P15144 Aminopeptidase N 80.16% 93.31%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.05% 100.00%

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.
Melia azedarach

Cross-Links

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PubChem 543438
NPASS NPC266320