Oct-1-EN-2-OL

Details

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Internal ID e284e702-0f21-4317-ad09-74b6d9fc2ed5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Enols
IUPAC Name oct-1-en-2-ol
SMILES (Canonical) CCCCCCC(=C)O
SMILES (Isomeric) CCCCCCC(=C)O
InChI InChI=1S/C8H16O/c1-3-4-5-6-7-8(2)9/h9H,2-7H2,1H3
InChI Key LNGYMCOWZUPVOA-UHFFFAOYSA-N
Popularity 7 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 3.30
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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142382-43-2
1-Octen-2-ol (9CI)
1-OCTEN-2-OL
SCHEMBL49642
DTXSID90572105

2D Structure

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2D Structure of Oct-1-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 + 0.9915 99.15%
Caco-2 + 0.8746 87.46%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Lysosomes 0.4141 41.41%
OATP2B1 inhibitior - 0.8454 84.54%
OATP1B1 inhibitior + 0.9158 91.58%
OATP1B3 inhibitior + 0.8849 88.49%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9515 95.15%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9311 93.11%
CYP3A4 substrate - 0.7308 73.08%
CYP2C9 substrate - 0.7957 79.57%
CYP2D6 substrate - 0.7785 77.85%
CYP3A4 inhibition - 0.9242 92.42%
CYP2C9 inhibition - 0.8976 89.76%
CYP2C19 inhibition - 0.8876 88.76%
CYP2D6 inhibition - 0.9295 92.95%
CYP1A2 inhibition + 0.6585 65.85%
CYP2C8 inhibition - 0.9196 91.96%
CYP inhibitory promiscuity - 0.7268 72.68%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6804 68.04%
Eye corrosion + 0.6085 60.85%
Eye irritation + 0.9779 97.79%
Skin irritation + 0.7371 73.71%
Skin corrosion - 0.8672 86.72%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7455 74.55%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7102 71.02%
skin sensitisation + 0.9238 92.38%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9362 93.62%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5157 51.57%
Acute Oral Toxicity (c) II 0.4868 48.68%
Estrogen receptor binding - 0.9502 95.02%
Androgen receptor binding - 0.8467 84.67%
Thyroid receptor binding - 0.7856 78.56%
Glucocorticoid receptor binding - 0.7745 77.45%
Aromatase binding - 0.8523 85.23%
PPAR gamma - 0.8121 81.21%
Honey bee toxicity - 0.9925 99.25%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity + 0.7441 74.41%
Fish aquatic toxicity + 0.9561 95.61%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.67% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 93.59% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.15% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.69% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.26% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.02% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.60% 97.29%
CHEMBL4040 P28482 MAP kinase ERK2 87.92% 83.82%
CHEMBL299 P17252 Protein kinase C alpha 85.01% 98.03%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.50% 92.86%
CHEMBL221 P23219 Cyclooxygenase-1 81.90% 90.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.44% 91.81%
CHEMBL2996 Q05655 Protein kinase C delta 80.74% 97.79%

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.
Trigonella foenum-graecum

Cross-Links

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PubChem 15372159
LOTUS LTS0100302
wikiData Q82460368