Methyl 3-acetyloxy-5-oxooxolane-2-carboxylate

Details

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Internal ID 10417be0-9ffd-4d9d-9e23-bb7a0627afcd
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name methyl 3-acetyloxy-5-oxooxolane-2-carboxylate
SMILES (Canonical) CC(=O)OC1CC(=O)OC1C(=O)OC
SMILES (Isomeric) CC(=O)OC1CC(=O)OC1C(=O)OC
InChI InChI=1S/C8H10O6/c1-4(9)13-5-3-6(10)14-7(5)8(11)12-2/h5,7H,3H2,1-2H3
InChI Key IANRRJBWWYZTPP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O6
Molecular Weight 202.16 g/mol
Exact Mass 202.04773803 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.59
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3-acetyloxy-5-oxooxolane-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 + 0.9267 92.67%
Caco-2 - 0.6625 66.25%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6981 69.81%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9314 93.14%
OATP1B3 inhibitior + 0.9469 94.69%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9687 96.87%
P-glycoprotein inhibitior - 0.9317 93.17%
P-glycoprotein substrate - 0.8962 89.62%
CYP3A4 substrate - 0.5055 50.55%
CYP2C9 substrate - 0.7939 79.39%
CYP2D6 substrate - 0.8786 87.86%
CYP3A4 inhibition - 0.9514 95.14%
CYP2C9 inhibition - 0.9460 94.60%
CYP2C19 inhibition - 0.7824 78.24%
CYP2D6 inhibition - 0.9520 95.20%
CYP1A2 inhibition - 0.7261 72.61%
CYP2C8 inhibition - 0.9495 94.95%
CYP inhibitory promiscuity - 0.8945 89.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9043 90.43%
Carcinogenicity (trinary) Non-required 0.6317 63.17%
Eye corrosion - 0.6929 69.29%
Eye irritation + 0.6651 66.51%
Skin irritation - 0.8425 84.25%
Skin corrosion - 0.9268 92.68%
Ames mutagenesis + 0.5553 55.53%
Human Ether-a-go-go-Related Gene inhibition - 0.7524 75.24%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5583 55.83%
skin sensitisation - 0.8828 88.28%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.8626 86.26%
Acute Oral Toxicity (c) III 0.4702 47.02%
Estrogen receptor binding - 0.7407 74.07%
Androgen receptor binding - 0.6783 67.83%
Thyroid receptor binding - 0.8203 82.03%
Glucocorticoid receptor binding - 0.8399 83.99%
Aromatase binding - 0.8340 83.40%
PPAR gamma - 0.8505 85.05%
Honey bee toxicity - 0.7839 78.39%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.6614 66.14%

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 95.30% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 87.74% 91.19%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.81% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.35% 85.14%
CHEMBL2581 P07339 Cathepsin D 85.69% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.35% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.24% 96.09%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 83.29% 83.10%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.88% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.52% 94.33%

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 162937380
LOTUS LTS0128363
wikiData Q105036198