2-Methoxy-3,5-dimethyl-6-undecylpyran-4-one

Details

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Internal ID 84d69ddb-783f-4eeb-9478-6415d577afd3
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 2-methoxy-3,5-dimethyl-6-undecylpyran-4-one
SMILES (Canonical) CCCCCCCCCCCC1=C(C(=O)C(=C(O1)OC)C)C
SMILES (Isomeric) CCCCCCCCCCCC1=C(C(=O)C(=C(O1)OC)C)C
InChI InChI=1S/C19H32O3/c1-5-6-7-8-9-10-11-12-13-14-17-15(2)18(20)16(3)19(21-4)22-17/h5-14H2,1-4H3
InChI Key NEZWAIZTXITFQQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H32O3
Molecular Weight 308.50 g/mol
Exact Mass 308.23514488 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.34
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methoxy-3,5-dimethyl-6-undecylpyran-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 + 0.9920 99.20%
Caco-2 + 0.7506 75.06%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7189 71.89%
OATP2B1 inhibitior - 0.8497 84.97%
OATP1B1 inhibitior + 0.9123 91.23%
OATP1B3 inhibitior + 0.9580 95.80%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6251 62.51%
P-glycoprotein inhibitior - 0.6084 60.84%
P-glycoprotein substrate - 0.8115 81.15%
CYP3A4 substrate - 0.5140 51.40%
CYP2C9 substrate - 0.8101 81.01%
CYP2D6 substrate - 0.8043 80.43%
CYP3A4 inhibition - 0.9011 90.11%
CYP2C9 inhibition - 0.8564 85.64%
CYP2C19 inhibition + 0.6464 64.64%
CYP2D6 inhibition - 0.9099 90.99%
CYP1A2 inhibition - 0.5296 52.96%
CYP2C8 inhibition - 0.7436 74.36%
CYP inhibitory promiscuity - 0.7324 73.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.7106 71.06%
Eye corrosion - 0.9553 95.53%
Eye irritation + 0.6564 65.64%
Skin irritation - 0.8077 80.77%
Skin corrosion - 0.9610 96.10%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6894 68.94%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6143 61.43%
skin sensitisation - 0.7944 79.44%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6101 61.01%
Acute Oral Toxicity (c) III 0.6361 63.61%
Estrogen receptor binding + 0.5783 57.83%
Androgen receptor binding - 0.4931 49.31%
Thyroid receptor binding + 0.5211 52.11%
Glucocorticoid receptor binding - 0.5895 58.95%
Aromatase binding + 0.5179 51.79%
PPAR gamma + 0.6994 69.94%
Honey bee toxicity - 0.9574 95.74%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6920 69.20%
Fish aquatic toxicity + 0.9728 97.28%

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
CHEMBL230 P35354 Cyclooxygenase-2 96.32% 89.63%
CHEMBL2581 P07339 Cathepsin D 94.54% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.27% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.12% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.20% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.90% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 85.56% 93.31%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.89% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.17% 91.11%
CHEMBL240 Q12809 HERG 82.36% 89.76%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.96% 94.00%

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 hieracioides
Podolepis rugata

Cross-Links

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PubChem 14539930
LOTUS LTS0181051
wikiData Q104396208