trans-3-Hexen-1-ol

Details

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Internal ID 712657c5-d61a-4840-9110-c718b9deb9f7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (E)-hex-3-en-1-ol
SMILES (Canonical) CCC=CCCO
SMILES (Isomeric) CC/C=C/CCO
InChI InChI=1S/C6H12O/c1-2-3-4-5-6-7/h3-4,7H,2,5-6H2,1H3/b4-3+
InChI Key UFLHIIWVXFIJGU-ONEGZZNKSA-N
Popularity 476 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O
Molecular Weight 100.16 g/mol
Exact Mass 100.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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928-97-2
(E)-Hex-3-en-1-ol
trans-3-Hexenol
trans-Hex-3-en-1-ol
(3E)-hex-3-en-1-ol
544-12-7
3-Hexen-1-ol
(E)-3-Hexen-1-ol
3-Hexen-1-ol, (E)-
3-Hexen-1-ol, (3E)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of trans-3-Hexen-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 + 0.9925 99.25%
Caco-2 + 0.9220 92.20%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5616 56.16%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8587 85.87%
OATP1B3 inhibitior + 0.9201 92.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9106 91.06%
P-glycoprotein inhibitior - 0.9830 98.30%
P-glycoprotein substrate - 0.9748 97.48%
CYP3A4 substrate - 0.7596 75.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9347 93.47%
CYP2C9 inhibition - 0.9230 92.30%
CYP2C19 inhibition - 0.9376 93.76%
CYP2D6 inhibition - 0.9509 95.09%
CYP1A2 inhibition - 0.6532 65.32%
CYP2C8 inhibition - 0.9850 98.50%
CYP inhibitory promiscuity - 0.8282 82.82%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6885 68.85%
Eye corrosion + 0.9058 90.58%
Eye irritation + 0.9817 98.17%
Skin irritation + 0.7930 79.30%
Skin corrosion - 0.9828 98.28%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6785 67.85%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6120 61.20%
skin sensitisation + 0.8353 83.53%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.5712 57.12%
Acute Oral Toxicity (c) III 0.8693 86.93%
Estrogen receptor binding - 0.9534 95.34%
Androgen receptor binding - 0.9383 93.83%
Thyroid receptor binding - 0.9051 90.51%
Glucocorticoid receptor binding - 0.8765 87.65%
Aromatase binding - 0.9206 92.06%
PPAR gamma - 0.8605 86.05%
Honey bee toxicity - 0.9775 97.75%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.6435 64.35%

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 84.28% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.94% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 83.54% 87.45%

Cross-Links

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PubChem 5284503
NPASS NPC63121
LOTUS LTS0001059
wikiData Q27259468