Hex-4-en-1-ol

Details

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Internal ID 9f055912-b11b-4f3c-9b25-9080fbc100f0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name hex-4-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H12O/c1-2-3-4-5-6-7/h2-3,7H,4-6H2,1H3
InChI Key VTIODUHBZHNXFP-UHFFFAOYSA-N
Popularity 8 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 1.20
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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4-Hexen-1-ol, (4Z)-
cis-1-Hydroxy-4-hexene
(E)-4-Hexenol
MFCD00009713
4-hexen-l-ol
hydroxypropyl propylene
DTXSID30862476
VTIODUHBZHNXFP-UHFFFAOYSA-N
AKOS028109167
SY066633
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Hex-4-en-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 + 0.9916 99.16%
Caco-2 + 0.8904 89.04%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.6810 68.10%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8051 80.51%
OATP1B3 inhibitior + 0.9262 92.62%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9190 91.90%
P-glycoprotein inhibitior - 0.9860 98.60%
P-glycoprotein substrate - 0.9649 96.49%
CYP3A4 substrate - 0.7111 71.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9418 94.18%
CYP2C9 inhibition - 0.9454 94.54%
CYP2C19 inhibition - 0.9367 93.67%
CYP2D6 inhibition - 0.9521 95.21%
CYP1A2 inhibition - 0.6626 66.26%
CYP2C8 inhibition - 0.9767 97.67%
CYP inhibitory promiscuity - 0.9215 92.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.7139 71.39%
Eye corrosion + 0.9210 92.10%
Eye irritation + 0.9547 95.47%
Skin irritation + 0.9106 91.06%
Skin corrosion - 0.5654 56.54%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6169 61.69%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5557 55.57%
skin sensitisation + 0.7219 72.19%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.9034 90.34%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.4773 47.73%
Acute Oral Toxicity (c) III 0.6362 63.62%
Estrogen receptor binding - 0.9225 92.25%
Androgen receptor binding - 0.8713 87.13%
Thyroid receptor binding - 0.8612 86.12%
Glucocorticoid receptor binding - 0.7522 75.22%
Aromatase binding - 0.9007 90.07%
PPAR gamma - 0.8441 84.41%
Honey bee toxicity - 0.9775 97.75%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.8514 85.14%

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 89.31% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.77% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 84.13% 87.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.45% 91.11%

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 61370
LOTUS LTS0121180
wikiData Q81986266