3-(4-Methoxy-5-methyl-6-oxopyran-2-yl)-2-methylprop-2-enoic acid

Details

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Internal ID 26668ae7-3d98-4bde-a441-5bfe857db007
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-(4-methoxy-5-methyl-6-oxopyran-2-yl)-2-methylprop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O5/c1-6(10(12)13)4-8-5-9(15-3)7(2)11(14)16-8/h4-5H,1-3H3,(H,12,13)
InChI Key VDGBGPADDGBBMF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O5
Molecular Weight 224.21 g/mol
Exact Mass 224.06847348 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.44
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Methoxy-5-methyl-6-oxopyran-2-yl)-2-methylprop-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9651 96.51%
Caco-2 + 0.8838 88.38%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8072 80.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9221 92.21%
OATP1B3 inhibitior + 0.9618 96.18%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9076 90.76%
P-glycoprotein inhibitior - 0.9359 93.59%
P-glycoprotein substrate - 0.9387 93.87%
CYP3A4 substrate - 0.5833 58.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9076 90.76%
CYP3A4 inhibition - 0.8838 88.38%
CYP2C9 inhibition - 0.9235 92.35%
CYP2C19 inhibition + 0.5169 51.69%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition - 0.7590 75.90%
CYP2C8 inhibition - 0.8141 81.41%
CYP inhibitory promiscuity - 0.6687 66.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8110 81.10%
Carcinogenicity (trinary) Non-required 0.5310 53.10%
Eye corrosion - 0.9395 93.95%
Eye irritation + 0.9093 90.93%
Skin irritation - 0.5994 59.94%
Skin corrosion - 0.9751 97.51%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6384 63.84%
Micronuclear + 0.7359 73.59%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation - 0.8531 85.31%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7864 78.64%
Acute Oral Toxicity (c) II 0.6455 64.55%
Estrogen receptor binding + 0.7176 71.76%
Androgen receptor binding - 0.4908 49.08%
Thyroid receptor binding - 0.7771 77.71%
Glucocorticoid receptor binding - 0.6396 63.96%
Aromatase binding + 0.5536 55.36%
PPAR gamma + 0.5641 56.41%
Honey bee toxicity - 0.9291 92.91%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9454 94.54%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.26% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.23% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.93% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.27% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.48% 94.00%
CHEMBL2581 P07339 Cathepsin D 85.26% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.72% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.49% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 81.99% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.05% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.04% 99.23%

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 85144949
LOTUS LTS0098537
wikiData Q104199249