(5Z,7S,12E)-tetradeca-5,12-dien-8,10-diyne-1,7,14-triol

Details

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Internal ID 51a8c724-61b2-4b69-97e3-cdc261d17692
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (5Z,7S,12E)-tetradeca-5,12-dien-8,10-diyne-1,7,14-triol
SMILES (Canonical) C(CCO)CC=CC(C#CC#CC=CCO)O
SMILES (Isomeric) C(CCO)C/C=C\[C@@H](C#CC#C/C=C/CO)O
InChI InChI=1S/C14H18O3/c15-12-8-4-1-2-6-10-14(17)11-7-3-5-9-13-16/h4,7-8,11,14-17H,3,5,9,12-13H2/b8-4+,11-7-/t14-/m1/s1
InChI Key HWZSORIFPSXFJZ-KMEUIEHISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O3
Molecular Weight 234.29 g/mol
Exact Mass 234.125594432 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.62
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5Z,7S,12E)-tetradeca-5,12-dien-8,10-diyne-1,7,14-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9009 90.09%
Caco-2 - 0.8160 81.60%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7362 73.62%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.8494 84.94%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9113 91.13%
P-glycoprotein inhibitior - 0.9410 94.10%
P-glycoprotein substrate - 0.8721 87.21%
CYP3A4 substrate - 0.5468 54.68%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.7581 75.81%
CYP3A4 inhibition - 0.8311 83.11%
CYP2C9 inhibition - 0.8629 86.29%
CYP2C19 inhibition - 0.8492 84.92%
CYP2D6 inhibition - 0.9465 94.65%
CYP1A2 inhibition - 0.7790 77.90%
CYP2C8 inhibition - 0.8345 83.45%
CYP inhibitory promiscuity - 0.7793 77.93%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.5826 58.26%
Eye corrosion + 0.6956 69.56%
Eye irritation - 0.8199 81.99%
Skin irritation - 0.5603 56.03%
Skin corrosion - 0.5408 54.08%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5429 54.29%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6424 64.24%
skin sensitisation - 0.6241 62.41%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.5560 55.60%
Acute Oral Toxicity (c) III 0.5031 50.31%
Estrogen receptor binding + 0.5324 53.24%
Androgen receptor binding - 0.7007 70.07%
Thyroid receptor binding - 0.5323 53.23%
Glucocorticoid receptor binding + 0.6961 69.61%
Aromatase binding + 0.6532 65.32%
PPAR gamma + 0.6616 66.16%
Honey bee toxicity - 0.7887 78.87%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8486 84.86%
Fish aquatic toxicity - 0.8628 86.28%

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 89.72% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 85.52% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.49% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.77% 91.11%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.08% 97.29%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 82.41% 95.58%
CHEMBL1937 Q92769 Histone deacetylase 2 81.73% 94.75%
CHEMBL2581 P07339 Cathepsin D 80.97% 98.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162895087
LOTUS LTS0054920
wikiData Q105034884