Oct-2-en-2-ol

Details

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Internal ID 07b1446f-ae8d-4b37-bb41-ceae733f7fa6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Enols
IUPAC Name oct-2-en-2-ol
SMILES (Canonical) CCCCCC=C(C)O
SMILES (Isomeric) CCCCCC=C(C)O
InChI InChI=1S/C8H16O/c1-3-4-5-6-7-8(2)9/h7,9H,3-6H2,1-2H3
InChI Key DKPIPSAKYWRSNN-UHFFFAOYSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O
Molecular Weight 128.21 g/mol
Exact Mass 128.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Oct-2-en-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.9509 95.09%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.3514 35.14%
OATP2B1 inhibitior - 0.8450 84.50%
OATP1B1 inhibitior + 0.8595 85.95%
OATP1B3 inhibitior + 0.9248 92.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9398 93.98%
P-glycoprotein inhibitior - 0.9890 98.90%
P-glycoprotein substrate - 0.9490 94.90%
CYP3A4 substrate - 0.7444 74.44%
CYP2C9 substrate - 0.7957 79.57%
CYP2D6 substrate - 0.7785 77.85%
CYP3A4 inhibition - 0.9228 92.28%
CYP2C9 inhibition - 0.8783 87.83%
CYP2C19 inhibition - 0.8820 88.20%
CYP2D6 inhibition - 0.8921 89.21%
CYP1A2 inhibition + 0.5881 58.81%
CYP2C8 inhibition - 0.9294 92.94%
CYP inhibitory promiscuity - 0.5111 51.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5731 57.31%
Eye corrosion + 0.7190 71.90%
Eye irritation + 0.9430 94.30%
Skin irritation + 0.5577 55.77%
Skin corrosion - 0.8392 83.92%
Ames mutagenesis - 0.8877 88.77%
Human Ether-a-go-go-Related Gene inhibition - 0.6507 65.07%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5401 54.01%
skin sensitisation + 0.9615 96.15%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.8412 84.12%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4504 45.04%
Acute Oral Toxicity (c) III 0.7127 71.27%
Estrogen receptor binding - 0.9567 95.67%
Androgen receptor binding - 0.8671 86.71%
Thyroid receptor binding - 0.8107 81.07%
Glucocorticoid receptor binding - 0.8687 86.87%
Aromatase binding - 0.9011 90.11%
PPAR gamma - 0.7838 78.38%
Honey bee toxicity - 0.9884 98.84%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.5755 57.55%
Fish aquatic toxicity + 0.9374 93.74%

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
CHEMBL2581 P07339 Cathepsin D 93.25% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.92% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.77% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.47% 97.29%
CHEMBL221 P23219 Cyclooxygenase-1 85.00% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.03% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.86% 93.56%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.67% 92.86%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.66% 96.95%

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.
Cymbopogon citratus

Cross-Links

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PubChem 53445325
LOTUS LTS0185465
wikiData Q104983570