Ethyl 5,6-dihydroxy-6-methyl-4-oxooxane-2-carboxylate

Details

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Internal ID ee87c77a-e202-4b34-b513-40afe0e3b8ba
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name ethyl 5,6-dihydroxy-6-methyl-4-oxooxane-2-carboxylate
SMILES (Canonical) CCOC(=O)C1CC(=O)C(C(O1)(C)O)O
SMILES (Isomeric) CCOC(=O)C1CC(=O)C(C(O1)(C)O)O
InChI InChI=1S/C9H14O6/c1-3-14-8(12)6-4-5(10)7(11)9(2,13)15-6/h6-7,11,13H,3-4H2,1-2H3
InChI Key RDJFMOKLERHSRJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O6
Molecular Weight 218.20 g/mol
Exact Mass 218.07903816 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP -1.00
Atomic LogP (AlogP) -1.02
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ethyl 5,6-dihydroxy-6-methyl-4-oxooxane-2-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7251 72.51%
Caco-2 - 0.7862 78.62%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8989 89.89%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9279 92.79%
OATP1B3 inhibitior + 0.9324 93.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9635 96.35%
P-glycoprotein inhibitior - 0.9493 94.93%
P-glycoprotein substrate - 0.9396 93.96%
CYP3A4 substrate + 0.5875 58.75%
CYP2C9 substrate - 0.8041 80.41%
CYP2D6 substrate - 0.8637 86.37%
CYP3A4 inhibition - 0.9401 94.01%
CYP2C9 inhibition - 0.8900 89.00%
CYP2C19 inhibition - 0.8628 86.28%
CYP2D6 inhibition - 0.9522 95.22%
CYP1A2 inhibition - 0.9190 91.90%
CYP2C8 inhibition - 0.9144 91.44%
CYP inhibitory promiscuity - 0.9737 97.37%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7272 72.72%
Eye corrosion - 0.9809 98.09%
Eye irritation - 0.8700 87.00%
Skin irritation - 0.8535 85.35%
Skin corrosion - 0.9449 94.49%
Ames mutagenesis - 0.7478 74.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7771 77.71%
Micronuclear - 0.6326 63.26%
Hepatotoxicity - 0.5433 54.33%
skin sensitisation - 0.9097 90.97%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5513 55.13%
Acute Oral Toxicity (c) III 0.6300 63.00%
Estrogen receptor binding + 0.6169 61.69%
Androgen receptor binding - 0.5535 55.35%
Thyroid receptor binding - 0.6537 65.37%
Glucocorticoid receptor binding + 0.5413 54.13%
Aromatase binding - 0.8336 83.36%
PPAR gamma - 0.6605 66.05%
Honey bee toxicity - 0.7948 79.48%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5350 53.50%
Fish aquatic toxicity + 0.6816 68.16%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.74% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.48% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.38% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.43% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.27% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.10% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.07% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.82% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.28% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.67% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.15% 90.17%

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 163060217
LOTUS LTS0264693
wikiData Q105234253