2-(3,5-Dioxo-4-phenyloxolan-2-ylidene)-2-phenylacetic acid

Details

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Internal ID 71a83887-e281-4d60-bdc0-030ba494e3f3
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones
IUPAC Name 2-(3,5-dioxo-4-phenyloxolan-2-ylidene)-2-phenylacetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H12O5/c19-15-13(11-7-3-1-4-8-11)18(22)23-16(15)14(17(20)21)12-9-5-2-6-10-12/h1-10,13H,(H,20,21)
InChI Key HUIYQDPOQUVMPX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H12O5
Molecular Weight 308.30 g/mol
Exact Mass 308.06847348 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3,5-Dioxo-4-phenyloxolan-2-ylidene)-2-phenylacetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9842 98.42%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7611 76.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9220 92.20%
OATP1B3 inhibitior + 0.9173 91.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6670 66.70%
P-glycoprotein inhibitior - 0.7888 78.88%
P-glycoprotein substrate - 0.9581 95.81%
CYP3A4 substrate - 0.6676 66.76%
CYP2C9 substrate + 0.6023 60.23%
CYP2D6 substrate - 0.8793 87.93%
CYP3A4 inhibition - 0.9418 94.18%
CYP2C9 inhibition - 0.6785 67.85%
CYP2C19 inhibition - 0.7106 71.06%
CYP2D6 inhibition - 0.9565 95.65%
CYP1A2 inhibition - 0.5932 59.32%
CYP2C8 inhibition - 0.6486 64.86%
CYP inhibitory promiscuity + 0.5343 53.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8671 86.71%
Carcinogenicity (trinary) Danger 0.4950 49.50%
Eye corrosion - 0.9797 97.97%
Eye irritation + 0.9056 90.56%
Skin irritation - 0.6025 60.25%
Skin corrosion - 0.9555 95.55%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7994 79.94%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.7465 74.65%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5214 52.14%
Acute Oral Toxicity (c) III 0.4799 47.99%
Estrogen receptor binding + 0.5384 53.84%
Androgen receptor binding + 0.7559 75.59%
Thyroid receptor binding - 0.6980 69.80%
Glucocorticoid receptor binding - 0.6450 64.50%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.5769 57.69%
Honey bee toxicity - 0.9615 96.15%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9921 99.21%

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 93.86% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.76% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.54% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 86.21% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.89% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 85.46% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.28% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.26% 97.09%

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 162859323
LOTUS LTS0114814
wikiData Q105033805