4-Hydroxy-3-methyl-5-(2-oxopropylidene)furan-2-one

Details

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Internal ID c69b95e8-2950-429e-a06e-115acf14fb0c
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 4-hydroxy-3-methyl-5-(2-oxopropylidene)furan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H8O4/c1-4(9)3-6-7(10)5(2)8(11)12-6/h3,10H,1-2H3
InChI Key UHBRGPQMMUQLOR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O4
Molecular Weight 168.15 g/mol
Exact Mass 168.04225873 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.85
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-3-methyl-5-(2-oxopropylidene)furan-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 + 0.9598 95.98%
Caco-2 + 0.6518 65.18%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7616 76.16%
OATP2B1 inhibitior - 0.8648 86.48%
OATP1B1 inhibitior + 0.9121 91.21%
OATP1B3 inhibitior + 0.9537 95.37%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9633 96.33%
P-glycoprotein inhibitior - 0.9714 97.14%
P-glycoprotein substrate - 0.9791 97.91%
CYP3A4 substrate - 0.5944 59.44%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8938 89.38%
CYP3A4 inhibition - 0.9657 96.57%
CYP2C9 inhibition - 0.9309 93.09%
CYP2C19 inhibition - 0.8387 83.87%
CYP2D6 inhibition - 0.9498 94.98%
CYP1A2 inhibition - 0.7927 79.27%
CYP2C8 inhibition - 0.9518 95.18%
CYP inhibitory promiscuity - 0.8881 88.81%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.8871 88.71%
Carcinogenicity (trinary) Danger 0.4238 42.38%
Eye corrosion - 0.7642 76.42%
Eye irritation + 0.9812 98.12%
Skin irritation + 0.5150 51.50%
Skin corrosion - 0.8070 80.70%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8598 85.98%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6908 69.08%
skin sensitisation - 0.7571 75.71%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6967 69.67%
Acute Oral Toxicity (c) III 0.3907 39.07%
Estrogen receptor binding - 0.7854 78.54%
Androgen receptor binding - 0.6121 61.21%
Thyroid receptor binding - 0.8714 87.14%
Glucocorticoid receptor binding - 0.7205 72.05%
Aromatase binding - 0.8158 81.58%
PPAR gamma - 0.8425 84.25%
Honey bee toxicity - 0.9208 92.08%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8315 83.15%

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 92.29% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.62% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.88% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.30% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.70% 89.00%
CHEMBL2581 P07339 Cathepsin D 84.68% 98.95%

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 76173461
LOTUS LTS0273016
wikiData Q104198209