Tetradeca-1,8,12-trien-10-yn-7-ol

Details

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Internal ID ea49bb72-3598-4eed-aa13-521f348904ba
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name tetradeca-1,8,12-trien-10-yn-7-ol
SMILES (Canonical) CC=CC#CC=CC(CCCCC=C)O
SMILES (Isomeric) CC=CC#CC=CC(CCCCC=C)O
InChI InChI=1S/C14H20O/c1-3-5-7-9-11-13-14(15)12-10-8-6-4-2/h3-5,11,13-15H,2,6,8,10,12H2,1H3
InChI Key FDFGZMGALLFLNJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O
Molecular Weight 204.31 g/mol
Exact Mass 204.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tetradeca-1,8,12-trien-10-yn-7-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9725 97.25%
Caco-2 + 0.5951 59.51%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.5051 50.51%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.8838 88.38%
OATP1B3 inhibitior + 0.9396 93.96%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6892 68.92%
P-glycoprotein inhibitior - 0.9650 96.50%
P-glycoprotein substrate - 0.8771 87.71%
CYP3A4 substrate - 0.5403 54.03%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.8373 83.73%
CYP2C9 inhibition - 0.8021 80.21%
CYP2C19 inhibition - 0.8070 80.70%
CYP2D6 inhibition - 0.9419 94.19%
CYP1A2 inhibition + 0.5674 56.74%
CYP2C8 inhibition - 0.8872 88.72%
CYP inhibitory promiscuity - 0.7323 73.23%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.5835 58.35%
Eye corrosion + 0.7707 77.07%
Eye irritation - 0.6150 61.50%
Skin irritation + 0.7719 77.19%
Skin corrosion + 0.6282 62.82%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6452 64.52%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6466 64.66%
skin sensitisation + 0.8309 83.09%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.9300 93.00%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6379 63.79%
Acute Oral Toxicity (c) II 0.7143 71.43%
Estrogen receptor binding - 0.6650 66.50%
Androgen receptor binding - 0.9331 93.31%
Thyroid receptor binding - 0.5947 59.47%
Glucocorticoid receptor binding + 0.7194 71.94%
Aromatase binding - 0.6361 63.61%
PPAR gamma - 0.6585 65.85%
Honey bee toxicity - 0.8035 80.35%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.5294 52.94%

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 91.73% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.72% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.92% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 85.57% 90.17%
CHEMBL206 P03372 Estrogen receptor alpha 84.24% 97.64%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.22% 91.11%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 83.41% 97.34%

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.
Baccharis pedunculata

Cross-Links

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PubChem 162927782
LOTUS LTS0056428
wikiData Q104993553