4-Ethylidene-3,5,5-trimethylcyclohex-2-en-1-one

Details

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Internal ID 3e00c69f-2c3b-485e-8944-ff48178944f3
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 4-ethylidene-3,5,5-trimethylcyclohex-2-en-1-one
SMILES (Canonical) CC=C1C(=CC(=O)CC1(C)C)C
SMILES (Isomeric) CC=C1C(=CC(=O)CC1(C)C)C
InChI InChI=1S/C11H16O/c1-5-10-8(2)6-9(12)7-11(10,3)4/h5-6H,7H2,1-4H3
InChI Key XFTQAVYYHITIQO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H16O
Molecular Weight 164.24 g/mol
Exact Mass 164.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Ethylidene-3,5,5-trimethylcyclohex-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.9550 95.50%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.5979 59.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8848 88.48%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7780 77.80%
P-glycoprotein inhibitior - 0.9828 98.28%
P-glycoprotein substrate - 0.9479 94.79%
CYP3A4 substrate - 0.5654 56.54%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8705 87.05%
CYP3A4 inhibition - 0.8417 84.17%
CYP2C9 inhibition - 0.8702 87.02%
CYP2C19 inhibition - 0.7170 71.70%
CYP2D6 inhibition - 0.9364 93.64%
CYP1A2 inhibition - 0.7784 77.84%
CYP2C8 inhibition - 0.9777 97.77%
CYP inhibitory promiscuity - 0.7712 77.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6617 66.17%
Carcinogenicity (trinary) Warning 0.4996 49.96%
Eye corrosion - 0.7208 72.08%
Eye irritation + 0.9382 93.82%
Skin irritation + 0.6829 68.29%
Skin corrosion - 0.9529 95.29%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6366 63.66%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6302 63.02%
skin sensitisation + 0.9648 96.48%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6520 65.20%
Acute Oral Toxicity (c) III 0.7239 72.39%
Estrogen receptor binding - 0.9784 97.84%
Androgen receptor binding - 0.7389 73.89%
Thyroid receptor binding - 0.8545 85.45%
Glucocorticoid receptor binding - 0.9053 90.53%
Aromatase binding - 0.8717 87.17%
PPAR gamma - 0.9263 92.63%
Honey bee toxicity - 0.9103 91.03%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8788 87.88%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.91% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.16% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 88.68% 94.75%
CHEMBL2581 P07339 Cathepsin D 85.11% 98.95%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.68% 85.30%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.87% 93.40%

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.
Castanopsis fissa

Cross-Links

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PubChem 72739000
LOTUS LTS0236923
wikiData Q105327287