1-Hydroxy-3-octanone

Details

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Internal ID c92515a0-f38d-44c5-a7ec-922bb18bdb80
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 1-hydroxyoctan-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H16O2/c1-2-3-4-5-8(10)6-7-9/h9H,2-7H2,1H3
InChI Key VGFJNJIGFHOBEJ-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O2
Molecular Weight 144.21 g/mol
Exact Mass 144.115029749 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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1-HYDROXYOCTAN-3-ONE
(2s)-hydroxy-3-octanone
SCHEMBL1022555
FEMA 2804
CHEBI:179949
DTXSID801315080
LMFA05000602
7786-52-9

2D Structure

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2D Structure of 1-Hydroxy-3-octanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9573 95.73%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5658 56.58%
OATP2B1 inhibitior - 0.8417 84.17%
OATP1B1 inhibitior + 0.9003 90.03%
OATP1B3 inhibitior + 0.8983 89.83%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.8973 89.73%
P-glycoprotein inhibitior - 0.9803 98.03%
P-glycoprotein substrate - 0.9322 93.22%
CYP3A4 substrate - 0.7163 71.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7863 78.63%
CYP3A4 inhibition - 0.9252 92.52%
CYP2C9 inhibition - 0.8876 88.76%
CYP2C19 inhibition - 0.8833 88.33%
CYP2D6 inhibition - 0.8771 87.71%
CYP1A2 inhibition + 0.5606 56.06%
CYP2C8 inhibition - 0.9630 96.30%
CYP inhibitory promiscuity - 0.8968 89.68%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.7390 73.90%
Eye corrosion + 0.7361 73.61%
Eye irritation + 0.9952 99.52%
Skin irritation + 0.6522 65.22%
Skin corrosion - 0.9233 92.33%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6914 69.14%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5619 56.19%
skin sensitisation + 0.4735 47.35%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.8887 88.87%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5878 58.78%
Acute Oral Toxicity (c) III 0.5593 55.93%
Estrogen receptor binding - 0.9729 97.29%
Androgen receptor binding - 0.9131 91.31%
Thyroid receptor binding - 0.8720 87.20%
Glucocorticoid receptor binding - 0.9192 91.92%
Aromatase binding - 0.9284 92.84%
PPAR gamma - 0.8538 85.38%
Honey bee toxicity - 0.9938 99.38%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.5360 53.60%
Fish aquatic toxicity - 0.5248 52.48%

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 93.55% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.38% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 92.84% 89.63%
CHEMBL2581 P07339 Cathepsin D 91.96% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.56% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.86% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.30% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.21% 85.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.03% 96.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.67% 91.81%
CHEMBL299 P17252 Protein kinase C alpha 80.92% 98.03%
CHEMBL2885 P07451 Carbonic anhydrase III 80.42% 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.
Vasconcellea pubescens

Cross-Links

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PubChem 13864714
LOTUS LTS0086814
wikiData Q105285770