3-Ethyl-2-methoxy-5-methyl-6-(10-oxoundecyl)pyran-4-one

Details

Top
Internal ID 0551a077-c2b2-4b6a-9625-97dfcfec62f3
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-ethyl-2-methoxy-5-methyl-6-(10-oxoundecyl)pyran-4-one
SMILES (Canonical) CCC1=C(OC(=C(C1=O)C)CCCCCCCCCC(=O)C)OC
SMILES (Isomeric) CCC1=C(OC(=C(C1=O)C)CCCCCCCCCC(=O)C)OC
InChI InChI=1S/C20H32O4/c1-5-17-19(22)16(3)18(24-20(17)23-4)14-12-10-8-6-7-9-11-13-15(2)21/h5-14H2,1-4H3
InChI Key FJEZQDOKVYOCMT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H32O4
Molecular Weight 336.50 g/mol
Exact Mass 336.23005950 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.77
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-Ethyl-2-methoxy-5-methyl-6-(10-oxoundecyl)pyran-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9782 97.82%
Caco-2 + 0.7556 75.56%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8187 81.87%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.8847 88.47%
OATP1B3 inhibitior + 0.9459 94.59%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7196 71.96%
P-glycoprotein inhibitior - 0.5182 51.82%
P-glycoprotein substrate - 0.7330 73.30%
CYP3A4 substrate + 0.5260 52.60%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.8079 80.79%
CYP3A4 inhibition - 0.7948 79.48%
CYP2C9 inhibition - 0.8952 89.52%
CYP2C19 inhibition + 0.6962 69.62%
CYP2D6 inhibition - 0.9219 92.19%
CYP1A2 inhibition - 0.5482 54.82%
CYP2C8 inhibition - 0.7570 75.70%
CYP inhibitory promiscuity - 0.8265 82.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.7452 74.52%
Eye corrosion - 0.9727 97.27%
Eye irritation - 0.5305 53.05%
Skin irritation - 0.8564 85.64%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8263 82.63%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5231 52.31%
skin sensitisation - 0.9024 90.24%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7210 72.10%
Acute Oral Toxicity (c) III 0.6237 62.37%
Estrogen receptor binding - 0.5154 51.54%
Androgen receptor binding + 0.5837 58.37%
Thyroid receptor binding - 0.4898 48.98%
Glucocorticoid receptor binding - 0.6191 61.91%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6275 62.75%
Honey bee toxicity - 0.9279 92.79%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5324 53.24%
Fish aquatic toxicity + 0.9854 98.54%

Targets

Top

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 94.58% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.36% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.23% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.01% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.53% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.87% 99.23%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.46% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.14% 86.33%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.83% 97.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.66% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.47% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 80.16% 94.73%

Plants that contains it

Top
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 hieracioides
Podolepis longipedata

Cross-Links

Top
PubChem 101704410
LOTUS LTS0175811
wikiData Q104996022