Methyl 4-(3-acetyl-2, 6-dihydroxyphenyl)-2-methoxybutanoate

Details

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Internal ID 524519b6-06ef-4e60-98f7-efd5c1247791
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name methyl 4-(3-acetyl-2,6-dihydroxyphenyl)-2-methoxybutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O6/c1-8(15)9-4-6-11(16)10(13(9)17)5-7-12(19-2)14(18)20-3/h4,6,12,16-17H,5,7H2,1-3H3
InChI Key WIMANBXYKSPMPI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O6
Molecular Weight 282.29 g/mol
Exact Mass 282.11033829 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.42
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 4-(3-acetyl-2, 6-dihydroxyphenyl)-2-methoxybutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8213 82.13%
Caco-2 + 0.8744 87.44%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7730 77.30%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.9119 91.19%
OATP1B3 inhibitior + 0.8391 83.91%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8984 89.84%
P-glycoprotein inhibitior - 0.8808 88.08%
P-glycoprotein substrate - 0.7010 70.10%
CYP3A4 substrate - 0.5118 51.18%
CYP2C9 substrate - 0.5869 58.69%
CYP2D6 substrate - 0.8645 86.45%
CYP3A4 inhibition - 0.8599 85.99%
CYP2C9 inhibition - 0.7494 74.94%
CYP2C19 inhibition - 0.7122 71.22%
CYP2D6 inhibition - 0.8634 86.34%
CYP1A2 inhibition - 0.6964 69.64%
CYP2C8 inhibition - 0.8089 80.89%
CYP inhibitory promiscuity - 0.9020 90.20%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8123 81.23%
Carcinogenicity (trinary) Non-required 0.7531 75.31%
Eye corrosion - 0.9770 97.70%
Eye irritation - 0.6072 60.72%
Skin irritation - 0.7425 74.25%
Skin corrosion - 0.9150 91.50%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4667 46.67%
Micronuclear - 0.7741 77.41%
Hepatotoxicity - 0.5974 59.74%
skin sensitisation - 0.8417 84.17%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6432 64.32%
Acute Oral Toxicity (c) III 0.6164 61.64%
Estrogen receptor binding + 0.6127 61.27%
Androgen receptor binding + 0.6557 65.57%
Thyroid receptor binding - 0.6187 61.87%
Glucocorticoid receptor binding + 0.5669 56.69%
Aromatase binding - 0.6906 69.06%
PPAR gamma - 0.7634 76.34%
Honey bee toxicity - 0.8737 87.37%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.9016 90.16%

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 98.09% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.88% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.92% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 89.32% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.21% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.50% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.74% 99.17%
CHEMBL3437 Q16853 Amine oxidase, copper containing 83.04% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.77% 86.33%

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 146684302
LOTUS LTS0027605
wikiData Q105306360