(4E,6E,10E,12E)-tetradeca-4,6,10,12-tetraen-8-yn-1-ol

Details

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Internal ID 6be1d2b2-89de-46d1-b3bd-aac9cbe50c1b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (4E,6E,10E,12E)-tetradeca-4,6,10,12-tetraen-8-yn-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h2-5,8-11,15H,12-14H2,1H3/b3-2+,5-4+,9-8+,11-10+
InChI Key DVVCIYWIFHPFME-BDPLZKCDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O
Molecular Weight 202.29 g/mol
Exact Mass 202.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4E,6E,10E,12E)-tetradeca-4,6,10,12-tetraen-8-yn-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 + 0.9869 98.69%
Caco-2 + 0.6599 65.99%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5286 52.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8198 81.98%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7301 73.01%
P-glycoprotein inhibitior - 0.9455 94.55%
P-glycoprotein substrate - 0.9053 90.53%
CYP3A4 substrate - 0.5781 57.81%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.8683 86.83%
CYP2C9 inhibition - 0.8803 88.03%
CYP2C19 inhibition - 0.9008 90.08%
CYP2D6 inhibition - 0.9548 95.48%
CYP1A2 inhibition - 0.5772 57.72%
CYP2C8 inhibition - 0.8975 89.75%
CYP inhibitory promiscuity - 0.8522 85.22%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6335 63.35%
Eye corrosion + 0.9049 90.49%
Eye irritation + 0.5788 57.88%
Skin irritation + 0.8430 84.30%
Skin corrosion + 0.6262 62.62%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4093 40.93%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5399 53.99%
skin sensitisation + 0.6035 60.35%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6133 61.33%
Acute Oral Toxicity (c) III 0.6021 60.21%
Estrogen receptor binding + 0.7602 76.02%
Androgen receptor binding - 0.5697 56.97%
Thyroid receptor binding + 0.5722 57.22%
Glucocorticoid receptor binding + 0.6959 69.59%
Aromatase binding + 0.7636 76.36%
PPAR gamma + 0.5700 57.00%
Honey bee toxicity - 0.9330 93.30%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7255 72.55%
Fish aquatic toxicity - 0.9119 91.19%

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 88.51% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.81% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.99% 99.17%
CHEMBL226 P30542 Adenosine A1 receptor 84.88% 95.93%

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.
Saussurea alpina

Cross-Links

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PubChem 101414495
LOTUS LTS0150251
wikiData Q104990373