Oct-6-en-4-ol

Details

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Internal ID d9001bf9-3896-4227-959d-f93893532ea7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name oct-6-en-4-ol
SMILES (Canonical) CCCC(CC=CC)O
SMILES (Isomeric) CCCC(CC=CC)O
InChI InChI=1S/C8H16O/c1-3-5-7-8(9)6-4-2/h3,5,8-9H,4,6-7H2,1-2H3
InChI Key KCDSGKHMSVPTOK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O
Molecular Weight 128.21 g/mol
Exact Mass 128.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Oct-6-en-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.8746 87.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.3458 34.58%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.8634 86.34%
OATP1B3 inhibitior + 0.9056 90.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9340 93.40%
P-glycoprotein inhibitior - 0.9845 98.45%
P-glycoprotein substrate - 0.9402 94.02%
CYP3A4 substrate - 0.6990 69.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7129 71.29%
CYP3A4 inhibition - 0.9323 93.23%
CYP2C9 inhibition - 0.9235 92.35%
CYP2C19 inhibition - 0.9102 91.02%
CYP2D6 inhibition - 0.9204 92.04%
CYP1A2 inhibition + 0.6969 69.69%
CYP2C8 inhibition - 0.9849 98.49%
CYP inhibitory promiscuity - 0.8007 80.07%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.7062 70.62%
Eye corrosion + 0.6960 69.60%
Eye irritation + 0.8428 84.28%
Skin irritation + 0.7227 72.27%
Skin corrosion - 0.8791 87.91%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5719 57.19%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6213 62.13%
skin sensitisation + 0.9511 95.11%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.9816 98.16%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.5912 59.12%
Acute Oral Toxicity (c) III 0.7903 79.03%
Estrogen receptor binding - 0.9120 91.20%
Androgen receptor binding - 0.9212 92.12%
Thyroid receptor binding - 0.8515 85.15%
Glucocorticoid receptor binding - 0.8559 85.59%
Aromatase binding - 0.9161 91.61%
PPAR gamma - 0.9032 90.32%
Honey bee toxicity - 0.9609 96.09%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.7327 73.27%

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 92.61% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.21% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.06% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 85.04% 93.31%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 83.48% 97.34%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.31% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.85% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 80.30% 83.82%

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.
Gossypium hirsutum

Cross-Links

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PubChem 57006309
LOTUS LTS0106436
wikiData Q105138684