3-Ethyl-2-methoxy-5-methyl-6-undecanoylpyran-4-one

Details

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Internal ID 744a1ff9-9ca4-45d1-bb17-1d5f4eee1f11
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones > Aryl alkyl ketones
IUPAC Name 3-ethyl-2-methoxy-5-methyl-6-undecanoylpyran-4-one
SMILES (Canonical) CCCCCCCCCCC(=O)C1=C(C(=O)C(=C(O1)OC)CC)C
SMILES (Isomeric) CCCCCCCCCCC(=O)C1=C(C(=O)C(=C(O1)OC)CC)C
InChI InChI=1S/C20H32O4/c1-5-7-8-9-10-11-12-13-14-17(21)19-15(3)18(22)16(6-2)20(23-4)24-19/h5-14H2,1-4H3
InChI Key OOMMYGUVENNSMC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O4
Molecular Weight 336.50 g/mol
Exact Mass 336.23005950 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.23
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Ethyl-2-methoxy-5-methyl-6-undecanoylpyran-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9667 96.67%
Caco-2 + 0.7658 76.58%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8049 80.49%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.8310 83.10%
OATP1B3 inhibitior + 0.9267 92.67%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6937 69.37%
P-glycoprotein inhibitior - 0.4850 48.50%
P-glycoprotein substrate - 0.7580 75.80%
CYP3A4 substrate + 0.5102 51.02%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.8079 80.79%
CYP3A4 inhibition - 0.8349 83.49%
CYP2C9 inhibition - 0.9339 93.39%
CYP2C19 inhibition + 0.7664 76.64%
CYP2D6 inhibition - 0.9346 93.46%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.7625 76.25%
CYP inhibitory promiscuity - 0.8535 85.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7149 71.49%
Eye corrosion - 0.9739 97.39%
Eye irritation + 0.6605 66.05%
Skin irritation - 0.8459 84.59%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6422 64.22%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5141 51.41%
skin sensitisation - 0.8849 88.49%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.5148 51.48%
Acute Oral Toxicity (c) III 0.6546 65.46%
Estrogen receptor binding + 0.5302 53.02%
Androgen receptor binding + 0.5709 57.09%
Thyroid receptor binding - 0.5514 55.14%
Glucocorticoid receptor binding - 0.5482 54.82%
Aromatase binding - 0.5608 56.08%
PPAR gamma + 0.5810 58.10%
Honey bee toxicity - 0.9616 96.16%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7873 78.73%
Fish aquatic toxicity + 0.9794 97.94%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 95.86% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.10% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.24% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.49% 96.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.24% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.61% 91.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.27% 95.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.15% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.55% 95.56%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.99% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.85% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.73% 91.81%

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.
Podolepis rugata

Cross-Links

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PubChem 14539937
LOTUS LTS0187397
wikiData Q105195475