1-(2,2,3-Trimethyl-6-methylidenecyclohexyl)pent-1-en-3-one

Details

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Internal ID fad3250c-1c0c-4bd2-955e-229cd951109f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-(2,2,3-trimethyl-6-methylidenecyclohexyl)pent-1-en-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-6-13(16)9-10-14-11(2)7-8-12(3)15(14,4)5/h9-10,12,14H,2,6-8H2,1,3-5H3
InChI Key MIRFZFVOZQLFTF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2,2,3-Trimethyl-6-methylidenecyclohexyl)pent-1-en-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 + 0.9955 99.55%
Caco-2 + 0.9072 90.72%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.3858 38.58%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9166 91.66%
OATP1B3 inhibitior + 0.8378 83.78%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9028 90.28%
P-glycoprotein inhibitior - 0.9241 92.41%
P-glycoprotein substrate - 0.8518 85.18%
CYP3A4 substrate + 0.5160 51.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8845 88.45%
CYP3A4 inhibition - 0.7911 79.11%
CYP2C9 inhibition - 0.8505 85.05%
CYP2C19 inhibition - 0.7974 79.74%
CYP2D6 inhibition - 0.9210 92.10%
CYP1A2 inhibition - 0.5711 57.11%
CYP2C8 inhibition - 0.7748 77.48%
CYP inhibitory promiscuity + 0.5089 50.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.5306 53.06%
Eye corrosion - 0.8689 86.89%
Eye irritation - 0.9114 91.14%
Skin irritation + 0.8358 83.58%
Skin corrosion - 0.9737 97.37%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5120 51.20%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5858 58.58%
skin sensitisation + 0.9437 94.37%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.8377 83.77%
Acute Oral Toxicity (c) III 0.7829 78.29%
Estrogen receptor binding - 0.7617 76.17%
Androgen receptor binding - 0.7053 70.53%
Thyroid receptor binding - 0.5300 53.00%
Glucocorticoid receptor binding - 0.6218 62.18%
Aromatase binding - 0.8223 82.23%
PPAR gamma - 0.7063 70.63%
Honey bee toxicity - 0.9095 90.95%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9689 96.89%

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 94.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.10% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.64% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 86.80% 90.17%
CHEMBL325 Q13547 Histone deacetylase 1 84.33% 95.92%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.90% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.76% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 81.89% 91.19%
CHEMBL2581 P07339 Cathepsin D 81.73% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.88% 99.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.75% 92.94%

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.
There are no matching plants.

Cross-Links

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PubChem 162967871
LOTUS LTS0203236
wikiData Q105165186