(2E,8E,10E)-2,8,10-Pentadecatriene-4,6-diyne

Details

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Internal ID 20134d51-bb74-4dcd-8619-5eaf7cffb6db
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (2E,8E,10E)-pentadeca-2,8,10-trien-4,6-diyne
SMILES (Canonical) CCCCC=CC=CC#CC#CC=CC
SMILES (Isomeric) CCCC/C=C/C=C/C#CC#C/C=C/C
InChI InChI=1S/C15H18/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h3,5,10,12,14-15H,4,6,8H2,1-2H3/b5-3+,12-10+,15-14+
InChI Key BXCQMFBOESMZEZ-DLDWCUKGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18
Molecular Weight 198.30 g/mol
Exact Mass 198.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 3.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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(2E,8E,10E)-2,8,10-Pentadecatriene-4,6-diyne

2D Structure

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2D Structure of (2E,8E,10E)-2,8,10-Pentadecatriene-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 + 0.9912 99.12%
Caco-2 + 0.8243 82.43%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4381 43.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8128 81.28%
OATP1B3 inhibitior + 0.9378 93.78%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7677 76.77%
P-glycoprotein inhibitior - 0.9484 94.84%
P-glycoprotein substrate - 0.8314 83.14%
CYP3A4 substrate - 0.5803 58.03%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9672 96.72%
CYP2C9 inhibition - 0.8984 89.84%
CYP2C19 inhibition - 0.9007 90.07%
CYP2D6 inhibition - 0.9387 93.87%
CYP1A2 inhibition - 0.5637 56.37%
CYP2C8 inhibition - 0.8621 86.21%
CYP inhibitory promiscuity - 0.6239 62.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.5337 53.37%
Eye corrosion + 0.9372 93.72%
Eye irritation + 0.6314 63.14%
Skin irritation + 0.8374 83.74%
Skin corrosion - 0.9057 90.57%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5072 50.72%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6213 62.13%
skin sensitisation + 0.9488 94.88%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.7834 78.34%
Acute Oral Toxicity (c) III 0.6182 61.82%
Estrogen receptor binding - 0.5269 52.69%
Androgen receptor binding - 0.6316 63.16%
Thyroid receptor binding + 0.6075 60.75%
Glucocorticoid receptor binding - 0.5750 57.50%
Aromatase binding + 0.5864 58.64%
PPAR gamma - 0.6234 62.34%
Honey bee toxicity - 0.9459 94.59%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9444 94.44%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.33% 92.08%
CHEMBL2581 P07339 Cathepsin D 88.51% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.97% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 87.90% 92.86%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 87.02% 96.42%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.15% 99.17%
CHEMBL2996 Q05655 Protein kinase C delta 85.99% 97.79%
CHEMBL1907 P15144 Aminopeptidase N 85.10% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.70% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 82.03% 89.63%
CHEMBL242 Q92731 Estrogen receptor beta 80.06% 98.35%

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.
Oenanthe aquatica
Oenanthe crocata

Cross-Links

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PubChem 92033506
LOTUS LTS0134475
wikiData Q104947866