(2E,8E,10E)-trideca-2,8,10,12-tetraen-4,6-diyn-1-ol

Details

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Internal ID 23339ee2-96d5-45c1-94ae-dc3d15f88f6d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (2E,8E,10E)-trideca-2,8,10,12-tetraen-4,6-diyn-1-ol
SMILES (Canonical) C=CC=CC=CC#CC#CC=CCO
SMILES (Isomeric) C=C/C=C/C=C/C#CC#C/C=C/CO
InChI InChI=1S/C13H12O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h2-6,11-12,14H,1,13H2/b4-3+,6-5+,12-11+
InChI Key HFQRXYXVQLBQFR-JHHIBIJLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O
Molecular Weight 184.23 g/mol
Exact Mass 184.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,8E,10E)-trideca-2,8,10,12-tetraen-4,6-diyn-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9798 97.98%
Caco-2 + 0.5560 55.60%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4844 48.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8982 89.82%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8330 83.30%
P-glycoprotein inhibitior - 0.9533 95.33%
P-glycoprotein substrate - 0.9579 95.79%
CYP3A4 substrate - 0.6002 60.02%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7902 79.02%
CYP3A4 inhibition - 0.9029 90.29%
CYP2C9 inhibition - 0.8832 88.32%
CYP2C19 inhibition - 0.8248 82.48%
CYP2D6 inhibition - 0.9648 96.48%
CYP1A2 inhibition - 0.6075 60.75%
CYP2C8 inhibition - 0.9231 92.31%
CYP inhibitory promiscuity - 0.8210 82.10%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.6083 60.83%
Carcinogenicity (trinary) Non-required 0.6345 63.45%
Eye corrosion + 0.9752 97.52%
Eye irritation + 0.5835 58.35%
Skin irritation + 0.8484 84.84%
Skin corrosion + 0.9581 95.81%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7387 73.87%
Micronuclear - 0.8341 83.41%
Hepatotoxicity - 0.5322 53.22%
skin sensitisation + 0.5562 55.62%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.7392 73.92%
Acute Oral Toxicity (c) II 0.5191 51.91%
Estrogen receptor binding - 0.6560 65.60%
Androgen receptor binding - 0.6481 64.81%
Thyroid receptor binding - 0.5723 57.23%
Glucocorticoid receptor binding - 0.5940 59.40%
Aromatase binding + 0.6336 63.36%
PPAR gamma + 0.5676 56.76%
Honey bee toxicity - 0.5000 50.00%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL4040 P28482 MAP kinase ERK2 90.53% 83.82%
CHEMBL1977 P11473 Vitamin D receptor 83.12% 99.43%
CHEMBL226 P30542 Adenosine A1 receptor 82.29% 95.93%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.45% 89.34%

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.
Dahlia sherffii

Cross-Links

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PubChem 101412326
LOTUS LTS0056406
wikiData Q105027477