cis-2-Hexen-1-ol

Details

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Internal ID 0bbc67be-a8b4-4095-968e-e770543e55a6
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (Z)-hex-2-en-1-ol
SMILES (Canonical) CCCC=CCO
SMILES (Isomeric) CCC/C=C\CO
InChI InChI=1S/C6H12O/c1-2-3-4-5-6-7/h4-5,7H,2-3,6H2,1H3/b5-4-
InChI Key ZCHHRLHTBGRGOT-PLNGDYQASA-N
Popularity 116 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 1.40
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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928-94-9
cis-Hex-2-en-1-ol
(Z)-hex-2-en-1-ol
2-Hexen-1-ol, (Z)-
2-Hexen-1-ol, (2Z)-
(Z)-2-Hexen-1-ol
2Z-Hexen-1-ol
(2Z)-2-Hexen-1-ol
UNII-871TEL510E
871TEL510E
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-2-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 + 0.9849 98.49%
Caco-2 + 0.9343 93.43%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.3974 39.74%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8963 89.63%
OATP1B3 inhibitior + 0.9317 93.17%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9278 92.78%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.9790 97.90%
CYP3A4 substrate - 0.7527 75.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9433 94.33%
CYP2C9 inhibition - 0.8892 88.92%
CYP2C19 inhibition - 0.9052 90.52%
CYP2D6 inhibition - 0.9310 93.10%
CYP1A2 inhibition - 0.6620 66.20%
CYP2C8 inhibition - 0.9815 98.15%
CYP inhibitory promiscuity - 0.7264 72.64%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.6026 60.26%
Eye corrosion + 0.9428 94.28%
Eye irritation + 0.9916 99.16%
Skin irritation + 0.6512 65.12%
Skin corrosion - 0.9868 98.68%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6446 64.46%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.8830 88.30%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5122 51.22%
Acute Oral Toxicity (c) III 0.8182 81.82%
Estrogen receptor binding - 0.9641 96.41%
Androgen receptor binding - 0.9236 92.36%
Thyroid receptor binding - 0.9023 90.23%
Glucocorticoid receptor binding - 0.8872 88.72%
Aromatase binding - 0.9220 92.20%
PPAR gamma - 0.9061 90.61%
Honey bee toxicity - 0.9826 98.26%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.8148 81.48%
Fish aquatic toxicity + 0.8316 83.16%

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 83.27% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.18% 99.17%

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.
Artemisia argyi
Artemisia montana
Artemisia princeps
Clinopodium nepeta subsp. spruneri
Olea europaea
Perilla frutescens

Cross-Links

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PubChem 5324489
NPASS NPC277604
LOTUS LTS0162420
wikiData Q1093153