1,3-Octadiene

Details

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Internal ID 336237e6-3e1e-4381-9351-0df3d51ff7e6
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name (3E)-octa-1,3-diene
SMILES (Canonical) CCCCC=CC=C
SMILES (Isomeric) CCCC/C=C/C=C
InChI InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h3,5,7H,1,4,6,8H2,2H3/b7-5+
InChI Key QTYUSOHYEPOHLV-FNORWQNLSA-N
Popularity 185 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14
Molecular Weight 110.20 g/mol
Exact Mass 110.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Octadiene
1002-33-1
(3E)-octa-1,3-diene
(E)-1,3-Octadiene
1,3-Octadiene, E
1,3-Octadiene, trans
UN2309
(3E)-1,3-Octadiene
63597-41-1
39491-65-1
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,3-Octadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 + 0.9419 94.19%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4330 43.30%
OATP2B1 inhibitior - 0.8656 86.56%
OATP1B1 inhibitior + 0.8711 87.11%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9258 92.58%
P-glycoprotein inhibitior - 0.9899 98.99%
P-glycoprotein substrate - 0.9403 94.03%
CYP3A4 substrate - 0.6669 66.69%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7603 76.03%
CYP3A4 inhibition - 0.9794 97.94%
CYP2C9 inhibition - 0.9236 92.36%
CYP2C19 inhibition - 0.8962 89.62%
CYP2D6 inhibition - 0.9432 94.32%
CYP1A2 inhibition - 0.5950 59.50%
CYP2C8 inhibition - 0.9439 94.39%
CYP inhibitory promiscuity - 0.7176 71.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.5162 51.62%
Eye corrosion + 0.9868 98.68%
Eye irritation + 0.9933 99.33%
Skin irritation + 0.8606 86.06%
Skin corrosion - 0.9327 93.27%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6386 63.86%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.9403 94.03%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.7145 71.45%
Acute Oral Toxicity (c) IV 0.4665 46.65%
Estrogen receptor binding - 0.9254 92.54%
Androgen receptor binding - 0.8162 81.62%
Thyroid receptor binding - 0.7591 75.91%
Glucocorticoid receptor binding - 0.6327 63.27%
Aromatase binding - 0.9021 90.21%
PPAR gamma - 0.7716 77.16%
Honey bee toxicity - 0.8900 89.00%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9609 96.09%

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
CHEMBL2581 P07339 Cathepsin D 87.44% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.45% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.37% 92.08%
CHEMBL2996 Q05655 Protein kinase C delta 85.01% 97.79%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.80% 97.29%
CHEMBL1907 P15144 Aminopeptidase N 84.50% 93.31%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.47% 92.86%
CHEMBL2885 P07451 Carbonic anhydrase III 84.30% 87.45%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.44% 97.34%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.79% 91.81%
CHEMBL230 P35354 Cyclooxygenase-2 81.07% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.31% 96.95%

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.
Cicuta virosa
Glycyrrhiza
Scleromitrion diffusum

Cross-Links

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PubChem 517653
NPASS NPC94189