3,5-Octadien-2-ol

Details

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Internal ID 9e5564d5-d758-405e-b07d-1f237aab2796
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (3E,5E)-octa-3,5-dien-2-ol
SMILES (Canonical) CCC=CC=CC(C)O
SMILES (Isomeric) CC/C=C/C=C/C(C)O
InChI InChI=1S/C8H14O/c1-3-4-5-6-7-8(2)9/h4-9H,3H2,1-2H3/b5-4+,7-6+
InChI Key RQQKJGCMOJSSOV-YTXTXJHMSA-N
Popularity 4 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 1.90
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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OCTA-3,5-DIEN-2-OL
SCHEMBL3273792
RQQKJGCMOJSSOV-YTXTXJHMSA-N
(3E,5E)-3,5-Octadien-2-ol #
EN300-7631808

2D Structure

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2D Structure of 3,5-Octadien-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.8899 88.99%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.4304 43.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9146 91.46%
OATP1B3 inhibitior + 0.9551 95.51%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8698 86.98%
P-glycoprotein inhibitior - 0.9862 98.62%
P-glycoprotein substrate - 0.9630 96.30%
CYP3A4 substrate - 0.7437 74.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7357 73.57%
CYP3A4 inhibition - 0.9532 95.32%
CYP2C9 inhibition - 0.8906 89.06%
CYP2C19 inhibition - 0.7893 78.93%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.7081 70.81%
CYP2C8 inhibition - 0.9860 98.60%
CYP inhibitory promiscuity - 0.7668 76.68%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6136 61.36%
Eye corrosion + 0.9097 90.97%
Eye irritation + 0.8204 82.04%
Skin irritation + 0.7807 78.07%
Skin corrosion - 0.5734 57.34%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7266 72.66%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5426 54.26%
skin sensitisation + 0.8087 80.87%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.6673 66.73%
Acute Oral Toxicity (c) III 0.8174 81.74%
Estrogen receptor binding - 0.9721 97.21%
Androgen receptor binding - 0.8474 84.74%
Thyroid receptor binding - 0.7772 77.72%
Glucocorticoid receptor binding - 0.8445 84.45%
Aromatase binding - 0.9282 92.82%
PPAR gamma - 0.8217 82.17%
Honey bee toxicity - 0.9481 94.81%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.6394 63.94%

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 90.78% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.86% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.44% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.33% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 83.06% 87.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.70% 89.34%

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.
Patrinia scabiosifolia
Patrinia villosa

Cross-Links

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PubChem 5364580
NPASS NPC184824