Phomobutenolide

Details

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Internal ID 7ea3901a-01ad-4c30-b5cd-2cc2b7057c0a
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 3-(3,4,5-trimethoxyphenyl)-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O5/c1-15-10-4-8(9-6-12(14)18-7-9)5-11(16-2)13(10)17-3/h4-6H,7H2,1-3H3
InChI Key NFMQBRBFFQGERC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O5
Molecular Weight 250.25 g/mol
Exact Mass 250.08412354 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.65
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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4-(3,4,5-trimethoxyphenyl)furan-2(5h)-one

2D Structure

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2D Structure of Phomobutenolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.8783 87.83%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.8100 81.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9729 97.29%
OATP1B3 inhibitior + 0.9607 96.07%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9381 93.81%
P-glycoprotein substrate - 0.9110 91.10%
CYP3A4 substrate - 0.5605 56.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8737 87.37%
CYP3A4 inhibition - 0.6590 65.90%
CYP2C9 inhibition - 0.5630 56.30%
CYP2C19 inhibition + 0.8358 83.58%
CYP2D6 inhibition - 0.9553 95.53%
CYP1A2 inhibition + 0.8207 82.07%
CYP2C8 inhibition - 0.8289 82.89%
CYP inhibitory promiscuity + 0.9324 93.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8928 89.28%
Carcinogenicity (trinary) Non-required 0.5602 56.02%
Eye corrosion - 0.9561 95.61%
Eye irritation + 0.7082 70.82%
Skin irritation - 0.7988 79.88%
Skin corrosion - 0.9819 98.19%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5351 53.51%
Micronuclear + 0.6214 62.14%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.7715 77.15%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4999 49.99%
Estrogen receptor binding + 0.6814 68.14%
Androgen receptor binding - 0.5852 58.52%
Thyroid receptor binding - 0.5196 51.96%
Glucocorticoid receptor binding - 0.5964 59.64%
Aromatase binding + 0.5934 59.34%
PPAR gamma - 0.7846 78.46%
Honey bee toxicity - 0.7603 76.03%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9738 97.38%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.68% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.78% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.11% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.26% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.10% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.83% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.88% 94.45%
CHEMBL2581 P07339 Cathepsin D 83.54% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.33% 96.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.68% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.06% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.39% 96.77%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 129882544
LOTUS LTS0149444
wikiData Q77373816