(5E)-5-ethylidene-3,6,6-trimethylpyran-2-one

Details

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Internal ID 4a602f7d-38da-419f-9707-1914e5491815
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name (5E)-5-ethylidene-3,6,6-trimethylpyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O2/c1-5-8-6-7(2)9(11)12-10(8,3)4/h5-6H,1-4H3/b8-5+
InChI Key OFOTZVNSRRCRCX-VMPITWQZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 2
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 (5E)-5-ethylidene-3,6,6-trimethylpyran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.8007 80.07%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7602 76.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8337 83.37%
OATP1B3 inhibitior + 0.9707 97.07%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8675 86.75%
P-glycoprotein inhibitior - 0.9637 96.37%
P-glycoprotein substrate - 0.9692 96.92%
CYP3A4 substrate - 0.5545 55.45%
CYP2C9 substrate - 0.7872 78.72%
CYP2D6 substrate - 0.8828 88.28%
CYP3A4 inhibition - 0.9069 90.69%
CYP2C9 inhibition - 0.9090 90.90%
CYP2C19 inhibition - 0.6875 68.75%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition - 0.7780 77.80%
CYP2C8 inhibition - 0.9285 92.85%
CYP inhibitory promiscuity - 0.7206 72.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7757 77.57%
Carcinogenicity (trinary) Non-required 0.5425 54.25%
Eye corrosion - 0.7547 75.47%
Eye irritation + 0.9651 96.51%
Skin irritation + 0.6927 69.27%
Skin corrosion - 0.9231 92.31%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5123 51.23%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.8052 80.52%
skin sensitisation + 0.7767 77.67%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.7900 79.00%
Acute Oral Toxicity (c) III 0.7211 72.11%
Estrogen receptor binding - 0.9209 92.09%
Androgen receptor binding - 0.8411 84.11%
Thyroid receptor binding - 0.8509 85.09%
Glucocorticoid receptor binding - 0.9098 90.98%
Aromatase binding - 0.7419 74.19%
PPAR gamma - 0.9447 94.47%
Honey bee toxicity - 0.8739 87.39%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7801 78.01%

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 95.24% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.30% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.17% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 87.87% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 87.59% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.20% 86.33%

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.
Plagius flosculosus

Cross-Links

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PubChem 14606175
LOTUS LTS0149451
wikiData Q105191327