Methyl 4-acetyloxy-3,5-dimethoxybenzoate

Details

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Internal ID bed159a5-52c9-4861-a5b5-d9c01127ac3c
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives > Gallic acid and derivatives
IUPAC Name methyl 4-acetyloxy-3,5-dimethoxybenzoate
SMILES (Canonical) CC(=O)OC1=C(C=C(C=C1OC)C(=O)OC)OC
SMILES (Isomeric) CC(=O)OC1=C(C=C(C=C1OC)C(=O)OC)OC
InChI InChI=1S/C12H14O6/c1-7(13)18-11-9(15-2)5-8(12(14)17-4)6-10(11)16-3/h5-6H,1-4H3
InChI Key LFGUHOLEYXHXKZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O6
Molecular Weight 254.24 g/mol
Exact Mass 254.07903816 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.42
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 4-acetyloxy-3,5-dimethoxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 + 0.7838 78.38%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8544 85.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9167 91.67%
OATP1B3 inhibitior + 0.9600 96.00%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7441 74.41%
P-glycoprotein inhibitior - 0.9197 91.97%
P-glycoprotein substrate - 0.9298 92.98%
CYP3A4 substrate - 0.6114 61.14%
CYP2C9 substrate - 0.5790 57.90%
CYP2D6 substrate - 0.8439 84.39%
CYP3A4 inhibition - 0.9245 92.45%
CYP2C9 inhibition - 0.9818 98.18%
CYP2C19 inhibition - 0.9070 90.70%
CYP2D6 inhibition - 0.9662 96.62%
CYP1A2 inhibition + 0.5164 51.64%
CYP2C8 inhibition - 0.6414 64.14%
CYP inhibitory promiscuity - 0.8753 87.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6917 69.17%
Carcinogenicity (trinary) Non-required 0.6525 65.25%
Eye corrosion - 0.5968 59.68%
Eye irritation + 0.9352 93.52%
Skin irritation - 0.7590 75.90%
Skin corrosion - 0.9555 95.55%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4255 42.55%
Micronuclear + 0.5407 54.07%
Hepatotoxicity + 0.5836 58.36%
skin sensitisation - 0.9197 91.97%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity + 0.7281 72.81%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.5682 56.82%
Acute Oral Toxicity (c) III 0.4484 44.84%
Estrogen receptor binding + 0.6025 60.25%
Androgen receptor binding - 0.7877 78.77%
Thyroid receptor binding - 0.7014 70.14%
Glucocorticoid receptor binding - 0.8027 80.27%
Aromatase binding - 0.5963 59.63%
PPAR gamma - 0.8138 81.38%
Honey bee toxicity - 0.8773 87.73%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9548 95.48%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.20% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.92% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.04% 91.11%
CHEMBL2535 P11166 Glucose transporter 87.72% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.88% 86.33%
CHEMBL4208 P20618 Proteasome component C5 84.23% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.25% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 81.04% 90.20%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.58% 81.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.32% 97.21%

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.
Phoenix dactylifera

Cross-Links

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PubChem 14299523
LOTUS LTS0244092
wikiData Q105151015