(Z)-4-Octen-1-ol

Details

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Internal ID cbc4ab78-8c51-4e2e-a8a6-2b03aa8052b5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (Z)-oct-4-en-1-ol
SMILES (Canonical) CCCC=CCCCO
SMILES (Isomeric) CCC/C=C\CCCO
InChI InChI=1S/C8H16O/c1-2-3-4-5-6-7-8-9/h4-5,9H,2-3,6-8H2,1H3/b5-4-
InChI Key OZQBPZSICOOLGU-PLNGDYQASA-N
Popularity 3 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) 2.12
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CIS-4-OCTENOL
cis-4-Octenol [FHFI]
4-Octen-1-ol, (Z)-
FEMA No. 4354
4-Octen-1-ol, (4Z)-
2XT1281K6U
54393-36-1
4-OCTEN-1-OL, CIS-
RefChem:526067
UNII-2XT1281K6U
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (Z)-4-Octen-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 + 0.9941 99.41%
Caco-2 + 0.9707 97.07%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.4345 43.45%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.8238 82.38%
OATP1B3 inhibitior + 0.9094 90.94%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8917 89.17%
P-glycoprotein inhibitior - 0.9803 98.03%
P-glycoprotein substrate - 0.9481 94.81%
CYP3A4 substrate - 0.7101 71.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9195 91.95%
CYP2C9 inhibition - 0.9024 90.24%
CYP2C19 inhibition - 0.9205 92.05%
CYP2D6 inhibition - 0.9344 93.44%
CYP1A2 inhibition - 0.5452 54.52%
CYP2C8 inhibition - 0.9560 95.60%
CYP inhibitory promiscuity - 0.8604 86.04%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6631 66.31%
Eye corrosion + 0.8175 81.75%
Eye irritation + 0.9912 99.12%
Skin irritation + 0.7076 70.76%
Skin corrosion - 0.9821 98.21%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5947 59.47%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6107 61.07%
skin sensitisation + 0.7991 79.91%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5085 50.85%
Acute Oral Toxicity (c) III 0.7701 77.01%
Estrogen receptor binding - 0.9595 95.95%
Androgen receptor binding - 0.8973 89.73%
Thyroid receptor binding - 0.8053 80.53%
Glucocorticoid receptor binding - 0.8388 83.88%
Aromatase binding - 0.9167 91.67%
PPAR gamma - 0.8292 82.92%
Honey bee toxicity - 0.9876 98.76%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8303 83.03%
Fish aquatic toxicity - 0.3839 38.39%

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 89.24% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 88.33% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.35% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.05% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.46% 96.95%
CHEMBL2581 P07339 Cathepsin D 81.75% 98.95%

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.
Acorus calamus var. angustatus

Cross-Links

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PubChem 5352836
NPASS NPC52195