1-Hexen-3-OL

Details

Top
Internal ID 0671fe95-de72-45b1-a2e0-cb0034664157
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name hex-1-en-3-ol
SMILES (Canonical) CCCC(C=C)O
SMILES (Isomeric) CCCC(C=C)O
InChI InChI=1S/C6H12O/c1-3-5-6(7)4-2/h4,6-7H,2-3,5H2,1H3
InChI Key BVOSSZSHBZQJOI-UHFFFAOYSA-N
Popularity 53 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H12O
Molecular Weight 100.16 g/mol
Exact Mass 100.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
Hex-1-en-3-ol
4798-44-1
Propylvinylcarbinol
3-Hydroxy-1-hexene
1-Vinylbutanol
Propyl vinyl carbinol
Vinyl propyl carbinol
1-Vinylbutan-1-ol
FEMA No. 3608
EINECS 225-355-0
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 1-Hexen-3-OL

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.7588 75.88%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Plasma membrane 0.3641 36.41%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9327 93.27%
OATP1B3 inhibitior + 0.9270 92.70%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9525 95.25%
P-glycoprotein inhibitior - 0.9843 98.43%
P-glycoprotein substrate - 0.9661 96.61%
CYP3A4 substrate - 0.7473 74.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6917 69.17%
CYP3A4 inhibition - 0.9347 93.47%
CYP2C9 inhibition - 0.9119 91.19%
CYP2C19 inhibition - 0.8248 82.48%
CYP2D6 inhibition - 0.9319 93.19%
CYP1A2 inhibition + 0.5290 52.90%
CYP2C8 inhibition - 0.9878 98.78%
CYP inhibitory promiscuity - 0.8499 84.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6377 63.77%
Eye corrosion + 0.8089 80.89%
Eye irritation + 0.9762 97.62%
Skin irritation + 0.7681 76.81%
Skin corrosion - 0.7061 70.61%
Ames mutagenesis - 0.8337 83.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6785 67.85%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6338 63.38%
skin sensitisation + 0.8565 85.65%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.5956 59.56%
Acute Oral Toxicity (c) II 0.6726 67.26%
Estrogen receptor binding - 0.8874 88.74%
Androgen receptor binding - 0.9718 97.18%
Thyroid receptor binding - 0.8618 86.18%
Glucocorticoid receptor binding - 0.7965 79.65%
Aromatase binding - 0.9188 91.88%
PPAR gamma - 0.9131 91.31%
Honey bee toxicity - 0.9340 93.40%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.5801 58.01%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 91.92% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.76% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.89% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 84.73% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.01% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.91% 97.25%

Plants that contains it

Top
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.
Angelica acutiloba
Angelica gigas
Angelica sinensis
Camellia sinensis
Clinopodium suaveolens
Salvia sclarea
Zea mays

Cross-Links

Top
PubChem 20928
NPASS NPC79544
LOTUS LTS0074606
wikiData Q27287030