2,6-Octadien-1-ol

Details

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Internal ID efe1d14d-10ee-46d9-b5aa-166a2b9268aa
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2E,6E)-octa-2,6-dien-1-ol
SMILES (Canonical) CC=CCCC=CCO
SMILES (Isomeric) C/C=C/CC/C=C/CO
InChI InChI=1S/C8H14O/c1-2-3-4-5-6-7-8-9/h2-3,6-7,9H,4-5,8H2,1H3/b3-2+,7-6+
InChI Key ONYJRUXYOCZIAW-BLWKUPHCSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O
Molecular Weight 126.20 g/mol
Exact Mass 126.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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SCHEMBL531232
SCHEMBL16556008
ONYJRUXYOCZIAW-BLWKUPHCSA-N
(2E,6Z)-2,6-Octadien-1-ol

2D Structure

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2D Structure of 2,6-Octadien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9835 98.35%
Caco-2 + 0.8776 87.76%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.6225 62.25%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.8660 86.60%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9090 90.90%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.9801 98.01%
CYP3A4 substrate - 0.7281 72.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9657 96.57%
CYP2C9 inhibition - 0.9113 91.13%
CYP2C19 inhibition - 0.9250 92.50%
CYP2D6 inhibition - 0.9416 94.16%
CYP1A2 inhibition - 0.7465 74.65%
CYP2C8 inhibition - 0.9866 98.66%
CYP inhibitory promiscuity - 0.8285 82.85%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6552 65.52%
Eye corrosion + 0.9523 95.23%
Eye irritation + 0.9876 98.76%
Skin irritation + 0.7868 78.68%
Skin corrosion - 0.9209 92.09%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6228 62.28%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.9124 91.24%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.9479 94.79%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.5625 56.25%
Acute Oral Toxicity (c) III 0.6991 69.91%
Estrogen receptor binding - 0.9511 95.11%
Androgen receptor binding - 0.9288 92.88%
Thyroid receptor binding - 0.8552 85.52%
Glucocorticoid receptor binding - 0.6354 63.54%
Aromatase binding - 0.9196 91.96%
PPAR gamma - 0.8027 80.27%
Honey bee toxicity - 0.9696 96.96%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.7808 78.08%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.75% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.59% 99.17%

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 6366591
NPASS NPC243725