3-(2-Hydroxypropan-2-yl)-6-methyl-6-(4-oxopentyl)cyclohex-2-en-1-one

Details

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Internal ID e9b1db3d-47eb-4d45-87cf-6c7a7c85c2c8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 3-(2-hydroxypropan-2-yl)-6-methyl-6-(4-oxopentyl)cyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O3/c1-11(16)6-5-8-15(4)9-7-12(10-13(15)17)14(2,3)18/h10,18H,5-9H2,1-4H3
InChI Key ZXXPRNDMFKXPMU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 0.90
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 3
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 3-(2-Hydroxypropan-2-yl)-6-methyl-6-(4-oxopentyl)cyclohex-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.8949 89.49%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.9078 90.78%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.8912 89.12%
OATP1B3 inhibitior + 0.9283 92.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.6064 60.64%
P-glycoprotein inhibitior - 0.9232 92.32%
P-glycoprotein substrate - 0.7164 71.64%
CYP3A4 substrate + 0.5566 55.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8843 88.43%
CYP3A4 inhibition - 0.6270 62.70%
CYP2C9 inhibition - 0.8021 80.21%
CYP2C19 inhibition - 0.8599 85.99%
CYP2D6 inhibition - 0.8945 89.45%
CYP1A2 inhibition - 0.9071 90.71%
CYP2C8 inhibition - 0.9142 91.42%
CYP inhibitory promiscuity - 0.8820 88.20%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8950 89.50%
Carcinogenicity (trinary) Non-required 0.6108 61.08%
Eye corrosion - 0.9821 98.21%
Eye irritation - 0.5277 52.77%
Skin irritation + 0.5439 54.39%
Skin corrosion - 0.9761 97.61%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8497 84.97%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6754 67.54%
skin sensitisation + 0.7161 71.61%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6496 64.96%
Acute Oral Toxicity (c) III 0.5499 54.99%
Estrogen receptor binding - 0.8121 81.21%
Androgen receptor binding + 0.5494 54.94%
Thyroid receptor binding - 0.6726 67.26%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.7838 78.38%
PPAR gamma - 0.6271 62.71%
Honey bee toxicity - 0.9178 91.78%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9915 99.15%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.53% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.81% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.58% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.73% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.53% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.97% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.35% 86.33%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.95% 82.69%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 16655282
LOTUS LTS0100766
wikiData Q105385893