Piperitenone

Details

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Internal ID 88e69343-6da3-4fdb-8643-a8f9f7ecbff1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 3-methyl-6-propan-2-ylidenecyclohex-2-en-1-one
SMILES (Canonical) CC1=CC(=O)C(=C(C)C)CC1
SMILES (Isomeric) CC1=CC(=O)C(=C(C)C)CC1
InChI InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)6-10(9)11/h6H,4-5H2,1-3H3
InChI Key HKZQJZIFODOLFR-UHFFFAOYSA-N
Popularity 277 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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491-09-8
3-Terpinolenone
Pulespenone
p-Mentha-1,4(8)-dien-3-one
2-CYCLOHEXEN-1-ONE, 3-METHYL-6-(1-METHYLETHYLIDENE)-
3-Methyl-6-(1-methylethylidene)-2-cyclohexen-1-one
3-methyl-6-propan-2-ylidenecyclohex-2-en-1-one
FEMA No. 3560
3-methyl-6-(propan-2-ylidene)cyclohex-2-en-1-one
3-Methyl-6-(1-methylethylidene)cyclohex-2-en-1-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Piperitenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.9556 95.56%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.4203 42.03%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9674 96.74%
OATP1B3 inhibitior + 0.9100 91.00%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8692 86.92%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9732 97.32%
CYP3A4 substrate - 0.6421 64.21%
CYP2C9 substrate - 0.6006 60.06%
CYP2D6 substrate - 0.8658 86.58%
CYP3A4 inhibition - 0.9664 96.64%
CYP2C9 inhibition - 0.8833 88.33%
CYP2C19 inhibition - 0.8188 81.88%
CYP2D6 inhibition - 0.9119 91.19%
CYP1A2 inhibition - 0.5562 55.62%
CYP2C8 inhibition - 0.9920 99.20%
CYP inhibitory promiscuity - 0.7458 74.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7710 77.10%
Carcinogenicity (trinary) Non-required 0.5395 53.95%
Eye corrosion - 0.7899 78.99%
Eye irritation + 0.9499 94.99%
Skin irritation + 0.8604 86.04%
Skin corrosion - 0.9014 90.14%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6695 66.95%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.8533 85.33%
skin sensitisation + 0.9395 93.95%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5899 58.99%
Acute Oral Toxicity (c) III 0.8168 81.68%
Estrogen receptor binding - 0.9801 98.01%
Androgen receptor binding - 0.6928 69.28%
Thyroid receptor binding - 0.8824 88.24%
Glucocorticoid receptor binding - 0.8243 82.43%
Aromatase binding - 0.9091 90.91%
PPAR gamma - 0.8572 85.72%
Honey bee toxicity - 0.9686 96.86%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9528 95.28%

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 93.78% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.22% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.68% 91.11%
CHEMBL4208 P20618 Proteasome component C5 83.81% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.72% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.14% 99.23%

Cross-Links

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PubChem 381152
NPASS NPC25771
LOTUS LTS0074451
wikiData Q27102310