methyl 3-hydroxy-5-(1-hydroxy-4-methoxy-4-oxobut-2-enylidene)-2H-pyran-4-carboxylate

Details

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Internal ID 2ef88ec1-9203-4a07-88b8-3134ed89245b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name methyl 3-hydroxy-5-(1-hydroxy-4-methoxy-4-oxobut-2-enylidene)-2H-pyran-4-carboxylate
SMILES (Canonical) COC(=O)C=CC(=C1COCC(=C1C(=O)OC)O)O
SMILES (Isomeric) COC(=O)C=CC(=C1COCC(=C1C(=O)OC)O)O
InChI InChI=1S/C12H14O7/c1-17-10(15)4-3-8(13)7-5-19-6-9(14)11(7)12(16)18-2/h3-4,13-14H,5-6H2,1-2H3
InChI Key ISDFYJLJSTWBAQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O7
Molecular Weight 270.23 g/mol
Exact Mass 270.07395278 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.54
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl 3-hydroxy-5-(1-hydroxy-4-methoxy-4-oxobut-2-enylidene)-2H-pyran-4-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7127 71.27%
Caco-2 + 0.5868 58.68%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8441 84.41%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9239 92.39%
OATP1B3 inhibitior + 0.9591 95.91%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8686 86.86%
P-glycoprotein inhibitior - 0.9410 94.10%
P-glycoprotein substrate - 0.8678 86.78%
CYP3A4 substrate + 0.5269 52.69%
CYP2C9 substrate - 0.8133 81.33%
CYP2D6 substrate - 0.8906 89.06%
CYP3A4 inhibition - 0.9859 98.59%
CYP2C9 inhibition - 0.9333 93.33%
CYP2C19 inhibition - 0.8402 84.02%
CYP2D6 inhibition - 0.9097 90.97%
CYP1A2 inhibition - 0.9066 90.66%
CYP2C8 inhibition - 0.7600 76.00%
CYP inhibitory promiscuity - 0.9842 98.42%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9028 90.28%
Carcinogenicity (trinary) Non-required 0.7350 73.50%
Eye corrosion - 0.9682 96.82%
Eye irritation + 0.7205 72.05%
Skin irritation - 0.7851 78.51%
Skin corrosion - 0.9455 94.55%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4893 48.93%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation - 0.8601 86.01%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5646 56.46%
Acute Oral Toxicity (c) III 0.5410 54.10%
Estrogen receptor binding + 0.8391 83.91%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5782 57.82%
Glucocorticoid receptor binding + 0.8044 80.44%
Aromatase binding + 0.5736 57.36%
PPAR gamma + 0.5519 55.19%
Honey bee toxicity - 0.9405 94.05%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.5683 56.83%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.54% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.65% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.76% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.28% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.84% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 82.68% 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 162816275
LOTUS LTS0055066
wikiData Q104169071