p-MENTH-8-EN-3-ONE, trans-

Details

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Internal ID efeab7ff-1b9b-4f06-8be9-5c4418a11ec9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (2R,5S)-5-methyl-2-prop-1-en-2-ylcyclohexan-1-one
SMILES (Canonical) CC1CCC(C(=O)C1)C(=C)C
SMILES (Isomeric) C[C@H]1CC[C@@H](C(=O)C1)C(=C)C
InChI InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)6-10(9)11/h8-9H,1,4-6H2,2-3H3/t8-,9+/m0/s1
InChI Key RMIANEGNSBUGDJ-DTWKUNHWSA-N
Popularity 179 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 2.80
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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D-Isopulegone
Isopulegone
(+)-Isopulegone
Isopulegone [FHFI]
p-MENTH-8-EN-3-ONE, trans-
Isopulegon
FEMA No. 2964
UNII-ERN62726IX
ERN62726IX
EINECS 249-725-6
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of p-MENTH-8-EN-3-ONE, trans-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.7756 77.56%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5743 57.43%
OATP2B1 inhibitior - 0.8398 83.98%
OATP1B1 inhibitior + 0.9437 94.37%
OATP1B3 inhibitior + 0.8863 88.63%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9420 94.20%
P-glycoprotein inhibitior - 0.9822 98.22%
P-glycoprotein substrate - 0.9141 91.41%
CYP3A4 substrate - 0.5851 58.51%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.7855 78.55%
CYP3A4 inhibition - 0.9166 91.66%
CYP2C9 inhibition - 0.9518 95.18%
CYP2C19 inhibition - 0.8753 87.53%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.7044 70.44%
CYP2C8 inhibition - 0.9808 98.08%
CYP inhibitory promiscuity - 0.8829 88.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5661 56.61%
Eye corrosion - 0.7064 70.64%
Eye irritation + 0.9727 97.27%
Skin irritation + 0.7146 71.46%
Skin corrosion - 0.9744 97.44%
Ames mutagenesis - 0.8728 87.28%
Human Ether-a-go-go-Related Gene inhibition - 0.7920 79.20%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.9125 91.25%
skin sensitisation + 0.9179 91.79%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.6145 61.45%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.8315 83.15%
Acute Oral Toxicity (c) III 0.8245 82.45%
Estrogen receptor binding - 0.9486 94.86%
Androgen receptor binding - 0.7163 71.63%
Thyroid receptor binding - 0.8483 84.83%
Glucocorticoid receptor binding - 0.7624 76.24%
Aromatase binding - 0.8305 83.05%
PPAR gamma - 0.8291 82.91%
Honey bee toxicity - 0.9177 91.77%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9882 98.82%

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 91.42% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.08% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.47% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.11% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 89.76% 91.49%
CHEMBL1902 P62942 FK506-binding protein 1A 87.82% 97.05%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.20% 95.56%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis
Cannabis sativa
Elettaria cardamomum
Litsea cubeba
Piper cubeba

Cross-Links

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PubChem 6432305
NPASS NPC11489
LOTUS LTS0241264
wikiData Q67880130