(4S,6S)-4-hydroxy-2,6-dimethyloct-7-en-3-one

Details

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Internal ID a4e22f55-c7c4-4fbf-a970-2325d9b68ea0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Acyloins
IUPAC Name (4S,6S)-4-hydroxy-2,6-dimethyloct-7-en-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O2/c1-5-8(4)6-9(11)10(12)7(2)3/h5,7-9,11H,1,6H2,2-4H3/t8-,9+/m1/s1
InChI Key HMGXDXWZMSVPMW-BDAKNGLRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.78
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S,6S)-4-hydroxy-2,6-dimethyloct-7-en-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9896 98.96%
Caco-2 + 0.5249 52.49%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5299 52.99%
OATP2B1 inhibitior - 0.8510 85.10%
OATP1B1 inhibitior + 0.9193 91.93%
OATP1B3 inhibitior + 0.9395 93.95%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7414 74.14%
P-glycoprotein inhibitior - 0.9769 97.69%
P-glycoprotein substrate - 0.9529 95.29%
CYP3A4 substrate - 0.6844 68.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7752 77.52%
CYP3A4 inhibition - 0.8445 84.45%
CYP2C9 inhibition - 0.9240 92.40%
CYP2C19 inhibition - 0.8411 84.11%
CYP2D6 inhibition - 0.9380 93.80%
CYP1A2 inhibition - 0.8292 82.92%
CYP2C8 inhibition - 0.9775 97.75%
CYP inhibitory promiscuity - 0.9396 93.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.5383 53.83%
Carcinogenicity (trinary) Non-required 0.7299 72.99%
Eye corrosion + 0.8548 85.48%
Eye irritation + 0.8241 82.41%
Skin irritation + 0.6581 65.81%
Skin corrosion - 0.7837 78.37%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6305 63.05%
Micronuclear - 0.8968 89.68%
Hepatotoxicity + 0.6409 64.09%
skin sensitisation + 0.9335 93.35%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.9473 94.73%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5393 53.93%
Acute Oral Toxicity (c) III 0.8325 83.25%
Estrogen receptor binding - 0.8827 88.27%
Androgen receptor binding - 0.6096 60.96%
Thyroid receptor binding - 0.8506 85.06%
Glucocorticoid receptor binding - 0.8187 81.87%
Aromatase binding - 0.8686 86.86%
PPAR gamma - 0.8996 89.96%
Honey bee toxicity - 0.9088 90.88%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.5068 50.68%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.02% 97.25%
CHEMBL2581 P07339 Cathepsin D 92.41% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 91.41% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.07% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.88% 96.47%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.85% 91.11%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.19% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.03% 89.34%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.14% 82.05%

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.
Tagetes minuta

Cross-Links

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PubChem 163000989
LOTUS LTS0226747
wikiData Q105030506