(5E,7E,9E,11E)-tetradeca-5,7,9,11-tetraen-1-ol

Details

Top
Internal ID 44250f0f-f019-4ba5-a25f-38229e2eac0c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (5E,7E,9E,11E)-tetradeca-5,7,9,11-tetraen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h3-10,15H,2,11-14H2,1H3/b4-3+,6-5+,8-7+,10-9+
InChI Key BLTWGWDMUNKAIK-BYFNFPHLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H22O
Molecular Weight 206.32 g/mol
Exact Mass 206.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (5E,7E,9E,11E)-tetradeca-5,7,9,11-tetraen-1-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9871 98.71%
Caco-2 + 0.9353 93.53%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4967 49.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8399 83.99%
OATP1B3 inhibitior + 0.9258 92.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6694 66.94%
P-glycoprotein inhibitior - 0.9401 94.01%
P-glycoprotein substrate - 0.9422 94.22%
CYP3A4 substrate - 0.6642 66.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7664 76.64%
CYP3A4 inhibition - 0.9221 92.21%
CYP2C9 inhibition - 0.8781 87.81%
CYP2C19 inhibition - 0.9158 91.58%
CYP2D6 inhibition - 0.9355 93.55%
CYP1A2 inhibition - 0.5808 58.08%
CYP2C8 inhibition - 0.9204 92.04%
CYP inhibitory promiscuity - 0.7929 79.29%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6211 62.11%
Eye corrosion + 0.8596 85.96%
Eye irritation + 0.9641 96.41%
Skin irritation + 0.8308 83.08%
Skin corrosion - 0.9014 90.14%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7210 72.10%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5285 52.85%
skin sensitisation + 0.7549 75.49%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.5540 55.40%
Acute Oral Toxicity (c) III 0.7855 78.55%
Estrogen receptor binding + 0.6326 63.26%
Androgen receptor binding - 0.6123 61.23%
Thyroid receptor binding + 0.5157 51.57%
Glucocorticoid receptor binding + 0.5974 59.74%
Aromatase binding + 0.6287 62.87%
PPAR gamma + 0.6396 63.96%
Honey bee toxicity - 0.9751 97.51%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.8081 80.81%
Fish aquatic toxicity - 0.7475 74.75%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.26% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.35% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 88.15% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.69% 97.29%
CHEMBL2581 P07339 Cathepsin D 83.39% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.67% 96.95%
CHEMBL226 P30542 Adenosine A1 receptor 81.18% 95.93%

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.
There are no matching plants.

Cross-Links

Top
PubChem 101415351
LOTUS LTS0263074
wikiData Q104938163