5-Hydroxy-4-octanone

Details

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Internal ID 8387171d-32e3-4cf2-8568-ad6570fc9c9f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides
IUPAC Name 5-hydroxyoctan-4-one
SMILES (Canonical) CCCC(C(=O)CCC)O
SMILES (Isomeric) CCCC(C(=O)CCC)O
InChI InChI=1S/C8H16O2/c1-3-5-7(9)8(10)6-4-2/h7,9H,3-6H2,1-2H3
InChI Key BVEYJWQCMOVMAR-UHFFFAOYSA-N
Popularity 15 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 1.40
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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5-Hydroxy-4-octanone
Butyroin
496-77-5
4-Octanone, 5-hydroxy-
5-Octanol-4-one
Octan-4-ol-5-one
FEMA No. 2587
WG070EDJ4X
NSC-1479
5-hydroxy-octan-4-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Hydroxy-4-octanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.8575 85.75%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6973 69.73%
OATP2B1 inhibitior - 0.8038 80.38%
OATP1B1 inhibitior + 0.9407 94.07%
OATP1B3 inhibitior + 0.9044 90.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9201 92.01%
P-glycoprotein inhibitior - 0.9742 97.42%
P-glycoprotein substrate - 0.9012 90.12%
CYP3A4 substrate - 0.7034 70.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7417 74.17%
CYP3A4 inhibition - 0.9464 94.64%
CYP2C9 inhibition - 0.8571 85.71%
CYP2C19 inhibition - 0.9032 90.32%
CYP2D6 inhibition - 0.9277 92.77%
CYP1A2 inhibition + 0.5422 54.22%
CYP2C8 inhibition - 0.9909 99.09%
CYP inhibitory promiscuity - 0.9246 92.46%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6743 67.43%
Eye corrosion + 0.8591 85.91%
Eye irritation + 0.9721 97.21%
Skin irritation + 0.5183 51.83%
Skin corrosion - 0.8701 87.01%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5649 56.49%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.8562 85.62%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7380 73.80%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5846 58.46%
Acute Oral Toxicity (c) III 0.7033 70.33%
Estrogen receptor binding - 0.9266 92.66%
Androgen receptor binding - 0.9236 92.36%
Thyroid receptor binding - 0.8828 88.28%
Glucocorticoid receptor binding - 0.9337 93.37%
Aromatase binding - 0.8987 89.87%
PPAR gamma - 0.9130 91.30%
Honey bee toxicity - 0.9782 97.82%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.5371 53.71%

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 94.01% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.12% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.80% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.62% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 83.96% 83.82%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.26% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 81.87% 93.31%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.61% 96.61%

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.
Camellia sinensis

Cross-Links

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PubChem 219794
LOTUS LTS0273851
wikiData Q27292617