2,4-Dimethoxy-6-acetylbenzoic acid methyl ester

Details

Top
Internal ID 903028cc-6401-4a2f-8e5f-e2e06e8316f8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name methyl 2-acetyl-4,6-dimethoxybenzoate
SMILES (Canonical) CC(=O)C1=C(C(=CC(=C1)OC)OC)C(=O)OC
SMILES (Isomeric) CC(=O)C1=C(C(=CC(=C1)OC)OC)C(=O)OC
InChI InChI=1S/C12H14O5/c1-7(13)9-5-8(15-2)6-10(16-3)11(9)12(14)17-4/h5-6H,1-4H3
InChI Key FTQDQZPPPLNVDC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C12H14O5
Molecular Weight 238.24 g/mol
Exact Mass 238.08412354 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
2,4-Dimethoxy-6-acetylbenzoic acid methyl ester

2D Structure

Top
2D Structure of 2,4-Dimethoxy-6-acetylbenzoic acid methyl ester

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9896 98.96%
Caco-2 + 0.6346 63.46%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8833 88.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9322 93.22%
OATP1B3 inhibitior + 0.9663 96.63%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8938 89.38%
P-glycoprotein inhibitior - 0.8874 88.74%
P-glycoprotein substrate - 0.8785 87.85%
CYP3A4 substrate - 0.6016 60.16%
CYP2C9 substrate - 0.7424 74.24%
CYP2D6 substrate - 0.8401 84.01%
CYP3A4 inhibition - 0.9251 92.51%
CYP2C9 inhibition - 0.9742 97.42%
CYP2C19 inhibition - 0.9390 93.90%
CYP2D6 inhibition - 0.9645 96.45%
CYP1A2 inhibition + 0.5435 54.35%
CYP2C8 inhibition - 0.6144 61.44%
CYP inhibitory promiscuity - 0.8478 84.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6279 62.79%
Carcinogenicity (trinary) Non-required 0.6978 69.78%
Eye corrosion - 0.5904 59.04%
Eye irritation + 0.9277 92.77%
Skin irritation - 0.7735 77.35%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6643 66.43%
Micronuclear + 0.5107 51.07%
Hepatotoxicity + 0.5677 56.77%
skin sensitisation - 0.9460 94.60%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity + 0.7281 72.81%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6794 67.94%
Acute Oral Toxicity (c) II 0.5655 56.55%
Estrogen receptor binding + 0.5368 53.68%
Androgen receptor binding - 0.6330 63.30%
Thyroid receptor binding - 0.5924 59.24%
Glucocorticoid receptor binding - 0.7017 70.17%
Aromatase binding - 0.5334 53.34%
PPAR gamma - 0.7092 70.92%
Honey bee toxicity - 0.8919 89.19%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9680 96.80%

Targets

Top

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.88% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.62% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.42% 91.11%
CHEMBL2535 P11166 Glucose transporter 89.60% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.21% 91.07%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.22% 95.50%
CHEMBL4208 P20618 Proteasome component C5 83.96% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.85% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.57% 81.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.33% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.32% 91.19%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.97% 96.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.72% 94.42%
CHEMBL4040 P28482 MAP kinase ERK2 82.57% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.56% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 81.34% 94.73%

Cross-Links

Top
PubChem 44577731
NPASS NPC202472
LOTUS LTS0234968
wikiData Q105001202