Methyl 2-hydroxy-2-methyl-4-(2-oxochromen-7-yl)oxybutanoate

Details

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Internal ID ba983b2a-c81a-4e96-a374-dabfcefccbe3
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name methyl 2-hydroxy-2-methyl-4-(2-oxochromen-7-yl)oxybutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O6/c1-15(18,14(17)19-2)7-8-20-11-5-3-10-4-6-13(16)21-12(10)9-11/h3-6,9,18H,7-8H2,1-2H3
InChI Key MHTLDLPKHVNQKS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O6
Molecular Weight 292.28 g/mol
Exact Mass 292.09468823 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.49
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 2-hydroxy-2-methyl-4-(2-oxochromen-7-yl)oxybutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9687 96.87%
Caco-2 + 0.5372 53.72%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7438 74.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8383 83.83%
OATP1B3 inhibitior + 0.8976 89.76%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6480 64.80%
P-glycoprotein inhibitior - 0.8273 82.73%
P-glycoprotein substrate - 0.8017 80.17%
CYP3A4 substrate + 0.5355 53.55%
CYP2C9 substrate - 0.6435 64.35%
CYP2D6 substrate - 0.8195 81.95%
CYP3A4 inhibition - 0.7304 73.04%
CYP2C9 inhibition - 0.8453 84.53%
CYP2C19 inhibition - 0.8492 84.92%
CYP2D6 inhibition - 0.9420 94.20%
CYP1A2 inhibition - 0.6544 65.44%
CYP2C8 inhibition + 0.4605 46.05%
CYP inhibitory promiscuity - 0.9463 94.63%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6478 64.78%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.9171 91.71%
Skin irritation - 0.7915 79.15%
Skin corrosion - 0.9413 94.13%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6785 67.85%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5708 57.08%
skin sensitisation - 0.9081 90.81%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7685 76.85%
Acute Oral Toxicity (c) III 0.6118 61.18%
Estrogen receptor binding + 0.7818 78.18%
Androgen receptor binding + 0.8665 86.65%
Thyroid receptor binding + 0.6188 61.88%
Glucocorticoid receptor binding + 0.8461 84.61%
Aromatase binding + 0.7613 76.13%
PPAR gamma + 0.6430 64.30%
Honey bee toxicity - 0.9244 92.44%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8586 85.86%

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 97.97% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.90% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.55% 94.00%
CHEMBL2581 P07339 Cathepsin D 91.99% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.34% 94.73%
CHEMBL4208 P20618 Proteasome component C5 89.36% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.42% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.18% 96.09%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.61% 81.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.55% 96.00%
CHEMBL2039 P27338 Monoamine oxidase B 80.54% 92.51%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.31% 95.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.30% 86.92%

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.
Melicope hayesii

Cross-Links

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PubChem 162901380
LOTUS LTS0111056
wikiData Q105164114