Delitpyrone E

Details

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Internal ID 9382bc4f-d68c-4587-b27a-6ed62dec4bb2
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 5-[(2S)-2-hydroxybutyl]-4-methoxy-6-methylpyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H16O4/c1-4-8(12)5-9-7(2)15-11(13)6-10(9)14-3/h6,8,12H,4-5H2,1-3H3/t8-/m0/s1
InChI Key GREACTBPWIMMPJ-QMMMGPOBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O4
Molecular Weight 212.24 g/mol
Exact Mass 212.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.27
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Delitpyrone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 + 0.8905 89.05%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7425 74.25%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.8816 88.16%
OATP1B3 inhibitior + 0.9363 93.63%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8414 84.14%
P-glycoprotein inhibitior - 0.9368 93.68%
P-glycoprotein substrate - 0.9003 90.03%
CYP3A4 substrate - 0.6120 61.20%
CYP2C9 substrate - 0.5903 59.03%
CYP2D6 substrate - 0.8349 83.49%
CYP3A4 inhibition - 0.9628 96.28%
CYP2C9 inhibition - 0.9380 93.80%
CYP2C19 inhibition - 0.7983 79.83%
CYP2D6 inhibition - 0.9360 93.60%
CYP1A2 inhibition - 0.8679 86.79%
CYP2C8 inhibition - 0.7883 78.83%
CYP inhibitory promiscuity - 0.8857 88.57%
UGT catelyzed + 0.7362 73.62%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.7369 73.69%
Eye corrosion - 0.9631 96.31%
Eye irritation + 0.5532 55.32%
Skin irritation - 0.6948 69.48%
Skin corrosion - 0.9694 96.94%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4528 45.28%
Micronuclear - 0.6582 65.82%
Hepatotoxicity + 0.5556 55.56%
skin sensitisation - 0.8287 82.87%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.7903 79.03%
Acute Oral Toxicity (c) III 0.6235 62.35%
Estrogen receptor binding - 0.8231 82.31%
Androgen receptor binding - 0.5397 53.97%
Thyroid receptor binding - 0.6656 66.56%
Glucocorticoid receptor binding - 0.7175 71.75%
Aromatase binding - 0.8742 87.42%
PPAR gamma + 0.5754 57.54%
Honey bee toxicity - 0.9126 91.26%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7393 73.93%

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 95.29% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 92.91% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.09% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.50% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.46% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.13% 94.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 90.51% 97.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.50% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.23% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.04% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.86% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 87.09% 94.73%
CHEMBL2535 P11166 Glucose transporter 84.05% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.84% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.96% 89.00%
CHEMBL4581 P52732 Kinesin-like protein 1 82.74% 93.18%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.12% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.63% 90.71%
CHEMBL4208 P20618 Proteasome component C5 80.84% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 80.45% 90.20%

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 139588658
LOTUS LTS0070962
wikiData Q105015798