Phomapyrone E

Details

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Internal ID e0d837b3-21db-45ae-b3ab-8aba8741fdeb
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 4-methoxy-3-methyl-6-[(E)-4-methyl-5-oxohex-2-en-2-yl]pyran-2-one
SMILES (Canonical) CC1=C(C=C(OC1=O)C(=CC(C)C(=O)C)C)OC
SMILES (Isomeric) CC1=C(C=C(OC1=O)/C(=C/C(C)C(=O)C)/C)OC
InChI InChI=1S/C14H18O4/c1-8(11(4)15)6-9(2)12-7-13(17-5)10(3)14(16)18-12/h6-8H,1-5H3/b9-6+
InChI Key MOPXMSJFYITBHO-RMKNXTFCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H18O4
Molecular Weight 250.29 g/mol
Exact Mass 250.12050905 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phomapyrone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9808 98.08%
Caco-2 + 0.6434 64.34%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7680 76.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8891 88.91%
OATP1B3 inhibitior + 0.9778 97.78%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7116 71.16%
P-glycoprotein inhibitior - 0.7050 70.50%
P-glycoprotein substrate - 0.8728 87.28%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5899 58.99%
CYP2D6 substrate - 0.8642 86.42%
CYP3A4 inhibition - 0.8279 82.79%
CYP2C9 inhibition - 0.9168 91.68%
CYP2C19 inhibition + 0.6843 68.43%
CYP2D6 inhibition - 0.9505 95.05%
CYP1A2 inhibition + 0.6384 63.84%
CYP2C8 inhibition - 0.7558 75.58%
CYP inhibitory promiscuity + 0.6175 61.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8284 82.84%
Carcinogenicity (trinary) Non-required 0.5950 59.50%
Eye corrosion - 0.9133 91.33%
Eye irritation - 0.8421 84.21%
Skin irritation - 0.6908 69.08%
Skin corrosion - 0.9775 97.75%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4052 40.52%
Micronuclear + 0.6859 68.59%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8515 85.15%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.8351 83.51%
Acute Oral Toxicity (c) II 0.5701 57.01%
Estrogen receptor binding - 0.5411 54.11%
Androgen receptor binding + 0.5195 51.95%
Thyroid receptor binding - 0.7464 74.64%
Glucocorticoid receptor binding - 0.6315 63.15%
Aromatase binding + 0.6780 67.80%
PPAR gamma + 0.6438 64.38%
Honey bee toxicity - 0.7893 78.93%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9614 96.14%

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
CHEMBL2581 P07339 Cathepsin D 94.13% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.51% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.62% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.34% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.87% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.92% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.64% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.56% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.32% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.18% 86.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.45% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.75% 91.07%
CHEMBL1255126 O15151 Protein Mdm4 82.52% 90.20%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.46% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.63% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 81.29% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.26% 97.21%

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 21580460
LOTUS LTS0084316
wikiData Q77494281