Heptadeca-2,8,10-trien-4,6-diyne

Details

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Internal ID 92fe8517-43cd-499f-a8ee-4190533e8876
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name heptadeca-2,8,10-trien-4,6-diyne
SMILES (Canonical) CCCCCCC=CC=CC#CC#CC=CC
SMILES (Isomeric) CCCCCCC=CC=CC#CC#CC=CC
InChI InChI=1S/C17H22/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3,5,14-17H,4,6,8,10,12H2,1-2H3
InChI Key KJZIXCGHDVCNHL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22
Molecular Weight 226.36 g/mol
Exact Mass 226.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 4.65
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Heptadeca-2,8,10-trien-4,6-diyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.8962 89.62%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.4685 46.85%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.8110 81.10%
OATP1B3 inhibitior + 0.9306 93.06%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7752 77.52%
P-glycoprotein inhibitior - 0.9190 91.90%
P-glycoprotein substrate - 0.8252 82.52%
CYP3A4 substrate - 0.5584 55.84%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9695 96.95%
CYP2C9 inhibition - 0.8881 88.81%
CYP2C19 inhibition - 0.9147 91.47%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition + 0.5673 56.73%
CYP2C8 inhibition - 0.7836 78.36%
CYP inhibitory promiscuity - 0.5830 58.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5561 55.61%
Eye corrosion + 0.9423 94.23%
Eye irritation - 0.4929 49.29%
Skin irritation + 0.8131 81.31%
Skin corrosion - 0.9728 97.28%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6926 69.26%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5996 59.96%
skin sensitisation + 0.9664 96.64%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6970 69.70%
Acute Oral Toxicity (c) III 0.8485 84.85%
Estrogen receptor binding - 0.5753 57.53%
Androgen receptor binding - 0.5526 55.26%
Thyroid receptor binding + 0.6486 64.86%
Glucocorticoid receptor binding - 0.6246 62.46%
Aromatase binding + 0.6100 61.00%
PPAR gamma - 0.4856 48.56%
Honey bee toxicity - 0.9475 94.75%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.9353 93.53%
Fish aquatic toxicity + 0.9935 99.35%

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
CHEMBL230 P35354 Cyclooxygenase-2 96.61% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.50% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 94.97% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 93.22% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.14% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.68% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 89.52% 90.17%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.28% 85.94%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.91% 97.29%
CHEMBL1907 P15144 Aminopeptidase N 85.10% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.04% 96.09%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 84.48% 96.42%
CHEMBL2885 P07451 Carbonic anhydrase III 84.47% 87.45%
CHEMBL2996 Q05655 Protein kinase C delta 82.22% 97.79%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.88% 96.00%

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.
Clibadium armanii
Oenanthe crocata

Cross-Links

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PubChem 153991204
LOTUS LTS0088682
wikiData Q105142066