2,9-Epoxydeliquinone

Details

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Internal ID 57a03a9e-91ed-4753-b4cd-d624cc220b1d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 3-(2-hydroxyethyl)-8-(hydroxymethyl)-4,8-dimethyl-10-oxatricyclo[4.3.1.01,6]dec-3-ene-2,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O5/c1-8-9(3-4-15)11(18)14-6-12(2,7-16)5-13(14,19-14)10(8)17/h15-16H,3-7H2,1-2H3
InChI Key DWSLSSYSNMZWGO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O5
Molecular Weight 266.29 g/mol
Exact Mass 266.11542367 g/mol
Topological Polar Surface Area (TPSA) 87.10 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.14
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,9-Epoxydeliquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9689 96.89%
Caco-2 + 0.7692 76.92%
Blood Brain Barrier + 0.7054 70.54%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7286 72.86%
OATP2B1 inhibitior - 0.8488 84.88%
OATP1B1 inhibitior + 0.8701 87.01%
OATP1B3 inhibitior + 0.9728 97.28%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5276 52.76%
BSEP inhibitior - 0.8381 83.81%
P-glycoprotein inhibitior - 0.9206 92.06%
P-glycoprotein substrate - 0.9335 93.35%
CYP3A4 substrate + 0.5295 52.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8483 84.83%
CYP3A4 inhibition - 0.7755 77.55%
CYP2C9 inhibition - 0.8450 84.50%
CYP2C19 inhibition - 0.9006 90.06%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition - 0.8513 85.13%
CYP2C8 inhibition - 0.8865 88.65%
CYP inhibitory promiscuity - 0.9529 95.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6676 66.76%
Eye corrosion - 0.9890 98.90%
Eye irritation + 0.5497 54.97%
Skin irritation - 0.6078 60.78%
Skin corrosion - 0.9354 93.54%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7412 74.12%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5323 53.23%
skin sensitisation - 0.8659 86.59%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.8391 83.91%
Acute Oral Toxicity (c) I 0.3879 38.79%
Estrogen receptor binding - 0.6438 64.38%
Androgen receptor binding + 0.7558 75.58%
Thyroid receptor binding + 0.5196 51.96%
Glucocorticoid receptor binding - 0.6063 60.63%
Aromatase binding - 0.5992 59.92%
PPAR gamma - 0.6356 63.56%
Honey bee toxicity - 0.9535 95.35%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9195 91.95%

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 92.01% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.38% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.10% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.63% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.48% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.23% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 15834664
LOTUS LTS0091657
wikiData Q77572543