Methyl 3-(3-formyl-4-methoxy-5-methyl-6-oxopyran-2-yl)prop-2-enoate

Details

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Internal ID 5ec8aa25-cdec-43aa-92a6-eb8e820d5b50
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name methyl 3-(3-formyl-4-methoxy-5-methyl-6-oxopyran-2-yl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12O6/c1-7-11(17-3)8(6-13)9(18-12(7)15)4-5-10(14)16-2/h4-6H,1-3H3
InChI Key AOUIWFQBPLFLEE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O6
Molecular Weight 252.22 g/mol
Exact Mass 252.06338810 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.96
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3-(3-formyl-4-methoxy-5-methyl-6-oxopyran-2-yl)prop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9728 97.28%
Caco-2 + 0.6318 63.18%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7655 76.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9045 90.45%
OATP1B3 inhibitior + 0.9834 98.34%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8689 86.89%
P-glycoprotein inhibitior - 0.7787 77.87%
P-glycoprotein substrate - 0.8989 89.89%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8878 88.78%
CYP3A4 inhibition - 0.8158 81.58%
CYP2C9 inhibition - 0.9622 96.22%
CYP2C19 inhibition - 0.8033 80.33%
CYP2D6 inhibition - 0.9570 95.70%
CYP1A2 inhibition + 0.5263 52.63%
CYP2C8 inhibition - 0.7915 79.15%
CYP inhibitory promiscuity - 0.6153 61.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8441 84.41%
Carcinogenicity (trinary) Non-required 0.5873 58.73%
Eye corrosion - 0.8330 83.30%
Eye irritation - 0.5288 52.88%
Skin irritation - 0.7302 73.02%
Skin corrosion - 0.9673 96.73%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5739 57.39%
Micronuclear + 0.6459 64.59%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9186 91.86%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.4888 48.88%
Acute Oral Toxicity (c) II 0.6022 60.22%
Estrogen receptor binding + 0.7583 75.83%
Androgen receptor binding + 0.5756 57.56%
Thyroid receptor binding - 0.7548 75.48%
Glucocorticoid receptor binding - 0.6198 61.98%
Aromatase binding + 0.8224 82.24%
PPAR gamma - 0.6323 63.23%
Honey bee toxicity - 0.9329 93.29%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9417 94.17%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.58% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.82% 95.56%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 93.68% 98.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.90% 96.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.50% 94.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.01% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.54% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.29% 89.00%

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 162949311
LOTUS LTS0167708
wikiData Q104085543