3-Cyclohexen-1-one, 2-isopropyl-5-methyl-

Details

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Internal ID b0d02b50-a43a-4553-bbf1-3c7c596c9527
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 5-methyl-2-propan-2-ylcyclohex-3-en-1-one
SMILES (Canonical) CC1CC(=O)C(C=C1)C(C)C
SMILES (Isomeric) CC1CC(=O)C(C=C1)C(C)C
InChI InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)6-10(9)11/h4-5,7-9H,6H2,1-3H3
InChI Key GPUOMCZFJZZLJT-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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GPUOMCZFJZZLJT-UHFFFAOYSA-N
2-Isopropyl-5-methyl-3-cyclohexen-1-one
2-Isopropyl-5-methyl-3-cyclohexene-1-one
2-Isopropyl-5-methyl-3-cyclohexen-1-one #

2D Structure

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2D Structure of 3-Cyclohexen-1-one, 2-isopropyl-5-methyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.6063 60.63%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6374 63.74%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9586 95.86%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9321 93.21%
P-glycoprotein inhibitior - 0.9814 98.14%
P-glycoprotein substrate - 0.9082 90.82%
CYP3A4 substrate - 0.6966 69.66%
CYP2C9 substrate - 0.8176 81.76%
CYP2D6 substrate - 0.8065 80.65%
CYP3A4 inhibition - 0.9352 93.52%
CYP2C9 inhibition - 0.9158 91.58%
CYP2C19 inhibition - 0.8914 89.14%
CYP2D6 inhibition - 0.9338 93.38%
CYP1A2 inhibition - 0.6696 66.96%
CYP2C8 inhibition - 0.9949 99.49%
CYP inhibitory promiscuity - 0.8799 87.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6427 64.27%
Carcinogenicity (trinary) Non-required 0.5577 55.77%
Eye corrosion + 0.7234 72.34%
Eye irritation + 0.9268 92.68%
Skin irritation + 0.7217 72.17%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7149 71.49%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.9650 96.50%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.5936 59.36%
Acute Oral Toxicity (c) III 0.5780 57.80%
Estrogen receptor binding - 0.9786 97.86%
Androgen receptor binding - 0.8260 82.60%
Thyroid receptor binding - 0.8955 89.55%
Glucocorticoid receptor binding - 0.8510 85.10%
Aromatase binding - 0.8911 89.11%
PPAR gamma - 0.9562 95.62%
Honey bee toxicity - 0.8350 83.50%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.8343 83.43%

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
CHEMBL2581 P07339 Cathepsin D 94.40% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.06% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.83% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.24% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.63% 97.25%

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
Xylopia aromatica
Zanthoxylum schinifolium

Cross-Links

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PubChem 573534
NPASS NPC288726
LOTUS LTS0050514
wikiData Q105015197