7-Octen-4-OL

Details

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Internal ID 7777512c-47ac-4f45-9e81-e26ec2e58853
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name oct-7-en-4-ol
SMILES (Canonical) CCCC(CCC=C)O
SMILES (Isomeric) CCCC(CCC=C)O
InChI InChI=1S/C8H16O/c1-3-5-7-8(9)6-4-2/h3,8-9H,1,4-7H2,2H3
InChI Key MJWKMORBWQZWOT-UHFFFAOYSA-N
Popularity 15 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 2.30
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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oct-7-en-4-ol
53907-72-5
SCHEMBL2474318
DTXSID40968695
MJWKMORBWQZWOT-UHFFFAOYSA-N
AKOS011019332
AS-56355
D93149

2D Structure

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2D Structure of 7-Octen-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 + 0.9925 99.25%
Caco-2 + 0.8448 84.48%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Plasma membrane 0.3965 39.65%
OATP2B1 inhibitior - 0.8396 83.96%
OATP1B1 inhibitior + 0.9307 93.07%
OATP1B3 inhibitior + 0.8888 88.88%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9315 93.15%
P-glycoprotein inhibitior - 0.9877 98.77%
P-glycoprotein substrate - 0.9431 94.31%
CYP3A4 substrate - 0.7062 70.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6917 69.17%
CYP3A4 inhibition - 0.9441 94.41%
CYP2C9 inhibition - 0.9089 90.89%
CYP2C19 inhibition - 0.9021 90.21%
CYP2D6 inhibition - 0.9435 94.35%
CYP1A2 inhibition + 0.6195 61.95%
CYP2C8 inhibition - 0.9848 98.48%
CYP inhibitory promiscuity - 0.8382 83.82%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.6634 66.34%
Eye corrosion + 0.7544 75.44%
Eye irritation + 0.9640 96.40%
Skin irritation + 0.7091 70.91%
Skin corrosion - 0.9213 92.13%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5478 54.78%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.9257 92.57%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9246 92.46%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5506 55.06%
Acute Oral Toxicity (c) III 0.4405 44.05%
Estrogen receptor binding - 0.9134 91.34%
Androgen receptor binding - 0.9356 93.56%
Thyroid receptor binding - 0.8803 88.03%
Glucocorticoid receptor binding - 0.7610 76.10%
Aromatase binding - 0.8553 85.53%
PPAR gamma - 0.9244 92.44%
Honey bee toxicity - 0.8891 88.91%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.8453 84.53%

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 91.35% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.09% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.36% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.85% 97.25%
CHEMBL2885 P07451 Carbonic anhydrase III 81.50% 87.45%

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.
Bupleurum chinense
Conocephalum conicum
Cucurbita maxima
Saposhnikovia divaricata

Cross-Links

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PubChem 40923
NPASS NPC112196
LOTUS LTS0079500
wikiData Q82951566