1,8,15-Heptadecatriene-11,13-diyne, (E,E)-

Details

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Internal ID 246fabc8-7f62-4180-a945-a1802d59a522
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (8E,15E)-heptadeca-1,8,15-trien-11,13-diyne
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3-4,6,15,17H,1,5,7,9,11,13,16H2,2H3/b6-4+,17-15+
InChI Key OJWVHJFAQCYGMT-FYBNGVAASA-N
Popularity 3 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 6.00
Atomic LogP (AlogP) 4.65
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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DTXSID601265378
28834-02-8
1,8,15-Heptadecatriene-11,13-diyne, (E,E)-
(8E,15E)-Heptadeca-1,8,15-triene-11,13-diyne

2D Structure

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2D Structure of 1,8,15-Heptadecatriene-11,13-diyne, (E,E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9810 98.10%
Caco-2 + 0.7641 76.41%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.3893 38.93%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.8382 83.82%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7123 71.23%
P-glycoprotein inhibitior - 0.9085 90.85%
P-glycoprotein substrate - 0.8242 82.42%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9504 95.04%
CYP2C9 inhibition - 0.8409 84.09%
CYP2C19 inhibition - 0.8799 87.99%
CYP2D6 inhibition - 0.9578 95.78%
CYP1A2 inhibition - 0.6055 60.55%
CYP2C8 inhibition - 0.7058 70.58%
CYP inhibitory promiscuity - 0.6083 60.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.4334 43.34%
Eye corrosion + 0.9778 97.78%
Eye irritation + 0.6053 60.53%
Skin irritation + 0.6981 69.81%
Skin corrosion - 0.9362 93.62%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4083 40.83%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.8698 86.98%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6888 68.88%
Acute Oral Toxicity (c) III 0.8397 83.97%
Estrogen receptor binding + 0.5705 57.05%
Androgen receptor binding - 0.7551 75.51%
Thyroid receptor binding + 0.5765 57.65%
Glucocorticoid receptor binding - 0.5175 51.75%
Aromatase binding + 0.5359 53.59%
PPAR gamma + 0.6584 65.84%
Honey bee toxicity - 0.8120 81.20%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9627 96.27%

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
CHEMBL240 Q12809 HERG 93.03% 89.76%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.58% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 88.52% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.81% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.15% 98.95%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 83.92% 92.95%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 83.75% 96.42%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.46% 95.17%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 80.85% 85.40%
CHEMBL2885 P07451 Carbonic anhydrase III 80.19% 87.45%

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.
Dahlia merckii

Cross-Links

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PubChem 19801361
LOTUS LTS0181534
wikiData Q105193334