1,7,9,15-Heptadecatetraene-11,13-diyne

Details

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Internal ID aef3b041-9c64-4259-9a7a-29f96ee98e43
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (7E,9E,15E)-heptadeca-1,7,9,15-tetraen-11,13-diyne
SMILES (Canonical) CC=CC#CC#CC=CC=CCCCCC=C
SMILES (Isomeric) C/C=C/C#CC#C/C=C/C=C/CCCCC=C
InChI InChI=1S/C17H20/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3-4,6,13,15-17H,1,5,7,9,11H2,2H3/b6-4+,15-13+,17-16+
InChI Key ZJZNMXVJKYOSGJ-GORQMSRHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20
Molecular Weight 224.34 g/mol
Exact Mass 224.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.43
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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62787-38-6

2D Structure

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2D Structure of 1,7,9,15-Heptadecatetraene-11,13-diyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9775 97.75%
Caco-2 + 0.8274 82.74%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.4007 40.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8496 84.96%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7191 71.91%
P-glycoprotein inhibitior - 0.9201 92.01%
P-glycoprotein substrate - 0.8672 86.72%
CYP3A4 substrate - 0.5288 52.88%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9215 92.15%
CYP2C9 inhibition - 0.8443 84.43%
CYP2C19 inhibition - 0.8716 87.16%
CYP2D6 inhibition - 0.9563 95.63%
CYP1A2 inhibition - 0.6012 60.12%
CYP2C8 inhibition - 0.8309 83.09%
CYP inhibitory promiscuity - 0.5757 57.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4043 40.43%
Eye corrosion + 0.9782 97.82%
Eye irritation + 0.5706 57.06%
Skin irritation + 0.7736 77.36%
Skin corrosion - 0.8790 87.90%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6589 65.89%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.8641 86.41%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7397 73.97%
Acute Oral Toxicity (c) III 0.6496 64.96%
Estrogen receptor binding + 0.7235 72.35%
Androgen receptor binding - 0.6096 60.96%
Thyroid receptor binding + 0.5891 58.91%
Glucocorticoid receptor binding - 0.4635 46.35%
Aromatase binding + 0.6449 64.49%
PPAR gamma + 0.6380 63.80%
Honey bee toxicity - 0.7866 78.66%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9200 92.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.10% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.87% 99.17%
CHEMBL242 Q92731 Estrogen receptor beta 82.43% 98.35%
CHEMBL2581 P07339 Cathepsin D 81.34% 98.95%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.31% 96.42%
CHEMBL221 P23219 Cyclooxygenase-1 80.29% 90.17%

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.
Bidens campylotheca
Coreopsis venusta
Dahlia australis
Dahlia merckii
Greenmaniella resinosa
Pleiotaxis rugosa

Cross-Links

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PubChem 6442686
LOTUS LTS0066951
wikiData Q105378297