Tetradeca-1,6,8,12-tetraen-10-yne

Details

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Internal ID 13b82c48-7f2f-4eb4-b806-7c4b2ba4c95b
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Acetylenes > Acyclic acetylenes > Alkatriynes
IUPAC Name tetradeca-1,6,8,12-tetraen-10-yne
SMILES (Canonical) CC=CC#CC=CC=CCCCC=C
SMILES (Isomeric) CC=CC#CC=CC=CCCCC=C
InChI InChI=1S/C14H18/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3-4,6,11-14H,1,5,7,9H2,2H3
InChI Key ZGQKXTROVMHNEH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H18
Molecular Weight 186.29 g/mol
Exact Mass 186.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.03
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tetradeca-1,6,8,12-tetraen-10-yne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 + 0.7870 78.70%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4323 43.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8255 82.55%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5595 55.95%
P-glycoprotein inhibitior - 0.9463 94.63%
P-glycoprotein substrate - 0.8853 88.53%
CYP3A4 substrate - 0.5352 53.52%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9392 93.92%
CYP2C9 inhibition - 0.8746 87.46%
CYP2C19 inhibition - 0.8838 88.38%
CYP2D6 inhibition - 0.9611 96.11%
CYP1A2 inhibition - 0.6916 69.16%
CYP2C8 inhibition - 0.8302 83.02%
CYP inhibitory promiscuity - 0.6479 64.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5900 59.00%
Carcinogenicity (trinary) Warning 0.3906 39.06%
Eye corrosion + 0.9827 98.27%
Eye irritation + 0.7733 77.33%
Skin irritation + 0.8108 81.08%
Skin corrosion - 0.7687 76.87%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4787 47.87%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.8326 83.26%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7285 72.85%
Acute Oral Toxicity (c) III 0.7675 76.75%
Estrogen receptor binding - 0.4862 48.62%
Androgen receptor binding - 0.8097 80.97%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7078 70.78%
Aromatase binding + 0.6545 65.45%
PPAR gamma - 0.5493 54.93%
Honey bee toxicity - 0.7733 77.33%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.7986 79.86%

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
CHEMBL242 Q92731 Estrogen receptor beta 90.90% 98.35%
CHEMBL1951 P21397 Monoamine oxidase A 82.52% 91.49%
CHEMBL206 P03372 Estrogen receptor alpha 82.11% 97.64%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.48% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.33% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.80% 96.09%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 80.65% 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 162911587
LOTUS LTS0205746
wikiData Q105375364