Methyl 3,5-dimethoxy-2-(6-methyl-4-oxopyran-3-carbonyl)benzoate

Details

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Internal ID c3c3f66e-7f2b-45f8-b726-51e8cbadf208
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Aryl-phenylketones
IUPAC Name methyl 3,5-dimethoxy-2-(6-methyl-4-oxopyran-3-carbonyl)benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O7/c1-9-5-13(18)12(8-24-9)16(19)15-11(17(20)23-4)6-10(21-2)7-14(15)22-3/h5-8H,1-4H3
InChI Key RELOYPIIFRWGAT-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O7
Molecular Weight 332.30 g/mol
Exact Mass 332.08960285 g/mol
Topological Polar Surface Area (TPSA) 88.10 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3,5-dimethoxy-2-(6-methyl-4-oxopyran-3-carbonyl)benzoate

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 + 0.8598 85.98%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7939 79.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9113 91.13%
OATP1B3 inhibitior + 0.9743 97.43%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6796 67.96%
P-glycoprotein inhibitior + 0.6723 67.23%
P-glycoprotein substrate - 0.8587 85.87%
CYP3A4 substrate + 0.5139 51.39%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.8740 87.40%
CYP3A4 inhibition - 0.8522 85.22%
CYP2C9 inhibition - 0.9168 91.68%
CYP2C19 inhibition - 0.7994 79.94%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition + 0.8673 86.73%
CYP2C8 inhibition - 0.5588 55.88%
CYP inhibitory promiscuity + 0.5440 54.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8813 88.13%
Carcinogenicity (trinary) Non-required 0.6429 64.29%
Eye corrosion - 0.9521 95.21%
Eye irritation + 0.5705 57.05%
Skin irritation - 0.8495 84.95%
Skin corrosion - 0.9844 98.44%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6417 64.17%
Micronuclear + 0.6659 66.59%
Hepatotoxicity + 0.5992 59.92%
skin sensitisation - 0.9755 97.55%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5721 57.21%
Acute Oral Toxicity (c) II 0.4761 47.61%
Estrogen receptor binding + 0.7921 79.21%
Androgen receptor binding + 0.6982 69.82%
Thyroid receptor binding + 0.5734 57.34%
Glucocorticoid receptor binding + 0.8005 80.05%
Aromatase binding + 0.6456 64.56%
PPAR gamma + 0.6640 66.40%
Honey bee toxicity - 0.9122 91.22%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9658 96.58%

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
CHEMBL3401 O75469 Pregnane X receptor 92.23% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.03% 94.00%
CHEMBL4208 P20618 Proteasome component C5 91.19% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.48% 95.50%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.90% 94.42%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.39% 91.11%
CHEMBL2535 P11166 Glucose transporter 87.63% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.52% 91.07%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.09% 95.56%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.94% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 85.12% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.95% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.13% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.74% 93.65%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.39% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.67% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 80.27% 91.19%

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 56947944
LOTUS LTS0200702
wikiData Q105234946