2,4,6-Trimethoxyl-3-methylacetophenone

Details

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Internal ID 05fa6d83-7f54-4aa0-880f-2b7e68b3bef5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2,4,6-trimethoxy-3-methylphenyl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O4/c1-7-9(14-3)6-10(15-4)11(8(2)13)12(7)16-5/h6H,1-5H3
InChI Key JUWLMMHIOBSJSI-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O4
Molecular Weight 224.25 g/mol
Exact Mass 224.10485899 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 4
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 2,4,6-Trimethoxyl-3-methylacetophenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.6565 65.65%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8865 88.65%
OATP2B1 inhibitior - 0.8642 86.42%
OATP1B1 inhibitior + 0.9165 91.65%
OATP1B3 inhibitior + 0.9879 98.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9106 91.06%
P-glycoprotein inhibitior - 0.9105 91.05%
P-glycoprotein substrate - 0.9545 95.45%
CYP3A4 substrate - 0.6260 62.60%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7499 74.99%
CYP3A4 inhibition - 0.7877 78.77%
CYP2C9 inhibition - 0.9858 98.58%
CYP2C19 inhibition - 0.6645 66.45%
CYP2D6 inhibition - 0.9628 96.28%
CYP1A2 inhibition + 0.7602 76.02%
CYP2C8 inhibition - 0.8101 81.01%
CYP inhibitory promiscuity - 0.5706 57.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6878 68.78%
Carcinogenicity (trinary) Non-required 0.6493 64.93%
Eye corrosion + 0.7493 74.93%
Eye irritation + 0.9697 96.97%
Skin irritation - 0.6134 61.34%
Skin corrosion - 0.9812 98.12%
Ames mutagenesis - 0.6664 66.64%
Human Ether-a-go-go-Related Gene inhibition - 0.6588 65.88%
Micronuclear - 0.5567 55.67%
Hepatotoxicity + 0.6565 65.65%
skin sensitisation - 0.8988 89.88%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.6526 65.26%
Acute Oral Toxicity (c) III 0.6248 62.48%
Estrogen receptor binding - 0.7345 73.45%
Androgen receptor binding - 0.7544 75.44%
Thyroid receptor binding - 0.6885 68.85%
Glucocorticoid receptor binding - 0.8231 82.31%
Aromatase binding - 0.6642 66.42%
PPAR gamma - 0.7620 76.20%
Honey bee toxicity - 0.9182 91.82%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6655 66.55%
Fish aquatic toxicity + 0.9139 91.39%

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 91.58% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.04% 97.21%
CHEMBL2535 P11166 Glucose transporter 85.71% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.62% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.35% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.23% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.63% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.29% 96.00%
CHEMBL4208 P20618 Proteasome component C5 81.75% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.69% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 80.26% 91.19%

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.
Euphorbia portulacoides

Cross-Links

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PubChem 11368088
LOTUS LTS0180425
wikiData Q105135466