Tetradeca-4,6-dien-8,10-diyne-1,12-diol

Details

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Internal ID 5bdb2d93-b402-475f-ac48-823778cee899
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name tetradeca-4,6-dien-8,10-diyne-1,12-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O2/c1-2-14(16)12-10-8-6-4-3-5-7-9-11-13-15/h3-5,7,14-16H,2,9,11,13H2,1H3
InChI Key DIGBHCWZAVSTEW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O2
Molecular Weight 218.29 g/mol
Exact Mass 218.130679813 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.65
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tetradeca-4,6-dien-8,10-diyne-1,12-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.7301 73.01%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5368 53.68%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.8239 82.39%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8632 86.32%
P-glycoprotein inhibitior - 0.9731 97.31%
P-glycoprotein substrate - 0.7728 77.28%
CYP3A4 substrate - 0.5299 52.99%
CYP2C9 substrate - 0.8056 80.56%
CYP2D6 substrate - 0.7828 78.28%
CYP3A4 inhibition - 0.7932 79.32%
CYP2C9 inhibition - 0.8608 86.08%
CYP2C19 inhibition - 0.8225 82.25%
CYP2D6 inhibition - 0.9274 92.74%
CYP1A2 inhibition - 0.5557 55.57%
CYP2C8 inhibition - 0.8398 83.98%
CYP inhibitory promiscuity - 0.6942 69.42%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6709 67.09%
Eye corrosion + 0.5612 56.12%
Eye irritation - 0.7883 78.83%
Skin irritation + 0.5230 52.30%
Skin corrosion - 0.6597 65.97%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3978 39.78%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5897 58.97%
skin sensitisation + 0.5219 52.19%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5294 52.94%
Estrogen receptor binding - 0.5272 52.72%
Androgen receptor binding - 0.5352 53.52%
Thyroid receptor binding + 0.5848 58.48%
Glucocorticoid receptor binding + 0.7415 74.15%
Aromatase binding + 0.5493 54.93%
PPAR gamma + 0.6596 65.96%
Honey bee toxicity - 0.9011 90.11%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7655 76.55%
Fish aquatic toxicity - 0.9372 93.72%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.02% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.94% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.77% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.36% 92.86%
CHEMBL2885 P07451 Carbonic anhydrase III 86.74% 87.45%
CHEMBL2581 P07339 Cathepsin D 86.32% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 86.11% 98.35%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.90% 96.95%
CHEMBL226 P30542 Adenosine A1 receptor 82.67% 95.93%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.58% 95.58%

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.
Cotula coronopifolia

Cross-Links

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PubChem 163040114
LOTUS LTS0229994
wikiData Q104981292