1-Acetoxy-p-menthane-3-one

Details

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Internal ID 4fb63c9e-7bf0-4541-b853-cf92a66b31ac
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (1-methyl-3-oxo-4-propan-2-ylcyclohexyl) acetate
SMILES (Canonical) CC(C)C1CCC(CC1=O)(C)OC(=O)C
SMILES (Isomeric) CC(C)C1CCC(CC1=O)(C)OC(=O)C
InChI InChI=1S/C12H20O3/c1-8(2)10-5-6-12(4,7-11(10)14)15-9(3)13/h8,10H,5-7H2,1-4H3
InChI Key HSDAHIORJOTSNZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O3
Molecular Weight 212.28 g/mol
Exact Mass 212.14124450 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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1-Acetoxy-p-menthane-3-one
HSDAHIORJOTSNZ-UHFFFAOYSA-N
4-Isopropyl-1-methyl-3-oxocyclohexyl acetate #

2D Structure

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2D Structure of 1-Acetoxy-p-menthane-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 + 0.9914 99.14%
Caco-2 + 0.5302 53.02%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.9046 90.46%
OATP2B1 inhibitior - 0.8499 84.99%
OATP1B1 inhibitior + 0.9525 95.25%
OATP1B3 inhibitior + 0.9752 97.52%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8975 89.75%
P-glycoprotein inhibitior - 0.9396 93.96%
P-glycoprotein substrate - 0.8227 82.27%
CYP3A4 substrate + 0.5422 54.22%
CYP2C9 substrate - 0.5955 59.55%
CYP2D6 substrate - 0.8655 86.55%
CYP3A4 inhibition - 0.9046 90.46%
CYP2C9 inhibition - 0.7207 72.07%
CYP2C19 inhibition - 0.7835 78.35%
CYP2D6 inhibition - 0.9564 95.64%
CYP1A2 inhibition - 0.8875 88.75%
CYP2C8 inhibition - 0.9793 97.93%
CYP inhibitory promiscuity - 0.9840 98.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8023 80.23%
Carcinogenicity (trinary) Non-required 0.5483 54.83%
Eye corrosion - 0.8465 84.65%
Eye irritation + 0.8110 81.10%
Skin irritation - 0.5176 51.76%
Skin corrosion - 0.9538 95.38%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6364 63.64%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.5477 54.77%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.8386 83.86%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6411 64.11%
Acute Oral Toxicity (c) III 0.7049 70.49%
Estrogen receptor binding - 0.9333 93.33%
Androgen receptor binding - 0.7353 73.53%
Thyroid receptor binding - 0.7996 79.96%
Glucocorticoid receptor binding - 0.7920 79.20%
Aromatase binding - 0.8350 83.50%
PPAR gamma - 0.9029 90.29%
Honey bee toxicity - 0.8814 88.14%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6950 69.50%
Fish aquatic toxicity + 0.9849 98.49%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.78% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.00% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 90.64% 93.04%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.99% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 86.00% 94.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.62% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 84.30% 91.19%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.51% 93.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.97% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.66% 85.14%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 557663
NPASS NPC258661
LOTUS LTS0005384
wikiData Q105110261