Octa-1,6-diene

Details

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Internal ID b5fcd1ad-0598-4447-adcf-c17cc7f2d342
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name octa-1,6-diene
SMILES (Canonical) CC=CCCCC=C
SMILES (Isomeric) CC=CCCCC=C
InChI InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h3-4,6H,1,5,7-8H2,2H3
InChI Key RJUCIROUEDJQIB-UHFFFAOYSA-N
Popularity 5 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 3.20
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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19036-81-8
octa-2,7-diene
DTXSID50940588
RJUCIROUEDJQIB-UHFFFAOYSA-N
AKOS028108397

2D Structure

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2D Structure of Octa-1,6-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.9075 90.75%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5186 51.86%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.8204 82.04%
OATP1B3 inhibitior + 0.9389 93.89%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9173 91.73%
P-glycoprotein inhibitior - 0.9856 98.56%
P-glycoprotein substrate - 0.9527 95.27%
CYP3A4 substrate - 0.6467 64.67%
CYP2C9 substrate - 0.8202 82.02%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9815 98.15%
CYP2C9 inhibition - 0.9426 94.26%
CYP2C19 inhibition - 0.9170 91.70%
CYP2D6 inhibition - 0.9570 95.70%
CYP1A2 inhibition - 0.7370 73.70%
CYP2C8 inhibition - 0.9422 94.22%
CYP inhibitory promiscuity - 0.7888 78.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.4836 48.36%
Eye corrosion + 0.9878 98.78%
Eye irritation + 0.9526 95.26%
Skin irritation + 0.9003 90.03%
Skin corrosion - 0.8337 83.37%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5537 55.37%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.9076 90.76%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5814 58.14%
Acute Oral Toxicity (c) III 0.5700 57.00%
Estrogen receptor binding - 0.9097 90.97%
Androgen receptor binding - 0.9303 93.03%
Thyroid receptor binding - 0.8326 83.26%
Glucocorticoid receptor binding - 0.6002 60.02%
Aromatase binding - 0.8507 85.07%
PPAR gamma - 0.7690 76.90%
Honey bee toxicity - 0.8773 87.73%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8825 88.25%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 84.87% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.70% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 82.99% 98.35%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.29% 97.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.13% 96.09%

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.
Tetradium ruticarpum

Cross-Links

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PubChem 19461
NPASS NPC13986