Tetradeca-4,6,12-triene-8,10-diyn-1-ol

Details

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Internal ID 42b9ae23-b2d4-4e11-b09d-d1db6edd674b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name tetradeca-4,6,12-trien-8,10-diyn-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H16O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h2-3,8-11,15H,12-14H2,1H3
InChI Key GSSKPCSIHXCRCA-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O
Molecular Weight 200.28 g/mol
Exact Mass 200.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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Tetradeca-4,6,12-triene-8,10-diyn-1-ol
DTXSID10779053

2D Structure

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2D Structure of Tetradeca-4,6,12-triene-8,10-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 + 0.9869 98.69%
Caco-2 + 0.6704 67.04%
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 + 0.8142 81.42%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8506 85.06%
P-glycoprotein inhibitior - 0.9601 96.01%
P-glycoprotein substrate - 0.8773 87.73%
CYP3A4 substrate - 0.5651 56.51%
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 - 0.8940 89.40%
CYP inhibitory promiscuity - 0.8522 85.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6335 63.35%
Eye corrosion + 0.9049 90.49%
Eye irritation + 0.5901 59.01%
Skin irritation + 0.8430 84.30%
Skin corrosion + 0.6262 62.62%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5679 56.79%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5274 52.74%
skin sensitisation + 0.6035 60.35%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.7134 71.34%
Acute Oral Toxicity (c) III 0.6021 60.21%
Estrogen receptor binding + 0.5882 58.82%
Androgen receptor binding - 0.6316 63.16%
Thyroid receptor binding + 0.5257 52.57%
Glucocorticoid receptor binding + 0.5564 55.64%
Aromatase binding + 0.6470 64.70%
PPAR gamma - 0.4936 49.36%
Honey bee toxicity - 0.9318 93.18%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7355 73.55%
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 88.81% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 87.15% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.99% 99.17%
CHEMBL226 P30542 Adenosine A1 receptor 83.83% 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.
Calea pinnatifida
Dahlia merckii
Dahlia scapigera
Dahlia sherffii

Cross-Links

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PubChem 71354562
LOTUS LTS0117880
wikiData Q82741752