cis-3-Hexen-1-ol

Details

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Internal ID 54eda70a-2fd4-4a1c-8860-719e33ce80a4
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (Z)-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-ARJAWSKDSA-N
Popularity 1,292 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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928-96-1
(Z)-Hex-3-en-1-ol
cis-3-Hexenol
Leaf alcohol
Blatteralkohol
(Z)-3-Hexen-1-ol
3-Hexenol
Z-3-Hexenol
3-Hexen-1-ol, (Z)-
(3Z)-hex-3-en-1-ol
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-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%

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.
Acacia paradoxa
Adonis sutchuenensis
Agastache rugosa
Ageratum conyzoides
Aizoon africanum
Alangium premnifolium
Aloe arborescens subsp. arborescens
Amaranthus retroflexus
Angelica tarokoensis
Anthriscus sylvestris
Artemisia annua
Artemisia argyi
Artemisia capillaris
Artemisia montana
Artemisia princeps
Artemisia scoparia
Astragalus ernestii
Berneuxia thibetica
Bombax ceiba
Bongardia chrysogonum
Brassica napus
Camellia saluenensis
Capsicum annuum
Crataegus pinnatifida
Diospyros ferrea
Epimedium davidii
Eragrostis curvula
Eriobotrya japonica
Erysimum odoratum
Fritillaria meleagris
Frullania tamarisci
Garcinia mangostana
Globba variabilis
Gossypium herbaceum
Heterotheca inuloides
Houttuynia cordata
Ilex amara
Isodon japonicus
Isophysis tasmanica
Knightia excelsa
Lasiosiphon lampranthus
Leonurus glaucescens
Lepidium draba
Lonicera japonica
Matricaria discoidea
Medicago sativa
Mentha arvensis
Mentha canadensis
Metasequoia glyptostroboides
Micromeria pineolens
Nepeta racemosa
Olea europaea
Perilla frutescens
Perilla frutescens var. crispa
Persicaria bistorta
Petasites japonicus
Philenoptera laxiflora
Phyllanthus emblica
Plantago lundborgii
Prunus armeniaca
Prunus persica
Pterocarpus indicus
Pueraria montana var. lobata
Punica granatum
Quercus agrifolia
Quercus petraea subsp. petraea
Robinia pseudoacacia
Salacia madagascariensis
Saussurea lyrata
Sideritis arborescens
Solanum acaule
Solanum pseudoquina
Swertia delavayi
Tanacetum parthenium
Thymus longicaulis
Triadica sebifera
Vaccinium vitis-idaea
Vepris hiernii
Viburnum dilatatum
Vismia jefensis
Zingiber officinale

Cross-Links

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PubChem 5281167
NPASS NPC197356
LOTUS LTS0132156
wikiData Q300850