1-(2-Methoxy-4-methylphenyl)ethanone

Details

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Internal ID 44a79d95-8be0-42ad-b005-f065a8d4dfe6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2-methoxy-4-methylphenyl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H12O2/c1-7-4-5-9(8(2)11)10(6-7)12-3/h4-6H,1-3H3
InChI Key WZHJIIIJSONKDI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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35633-35-3
1-(2-methoxy-4-methylphenyl)ethan-1-one
MFCD08239634
2'-Methoxy-4'-methylacetophenone
1-(2-Methoxy-4-methylphenyl)-ethanone
CHEMBL447133
SCHEMBL2064454
DTXSID80429371
AKOS000295790
BS-50922
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-(2-Methoxy-4-methylphenyl)ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9146 91.46%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.9065 90.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9677 96.77%
OATP1B3 inhibitior + 0.9861 98.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8839 88.39%
P-glycoprotein inhibitior - 0.9629 96.29%
P-glycoprotein substrate - 0.9503 95.03%
CYP3A4 substrate - 0.6699 66.99%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7499 74.99%
CYP3A4 inhibition - 0.9452 94.52%
CYP2C9 inhibition - 0.9891 98.91%
CYP2C19 inhibition - 0.7108 71.08%
CYP2D6 inhibition - 0.9637 96.37%
CYP1A2 inhibition + 0.8042 80.42%
CYP2C8 inhibition - 0.7790 77.90%
CYP inhibitory promiscuity - 0.6617 66.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6655 66.55%
Carcinogenicity (trinary) Non-required 0.5959 59.59%
Eye corrosion + 0.9158 91.58%
Eye irritation + 0.9959 99.59%
Skin irritation + 0.6317 63.17%
Skin corrosion - 0.9465 94.65%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6148 61.48%
Micronuclear - 0.6567 65.67%
Hepatotoxicity + 0.5565 55.65%
skin sensitisation - 0.5358 53.58%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6779 67.79%
Acute Oral Toxicity (c) III 0.8648 86.48%
Estrogen receptor binding - 0.8989 89.89%
Androgen receptor binding - 0.8229 82.29%
Thyroid receptor binding - 0.7999 79.99%
Glucocorticoid receptor binding - 0.9084 90.84%
Aromatase binding - 0.7417 74.17%
PPAR gamma - 0.8931 89.31%
Honey bee toxicity - 0.9629 96.29%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6707 67.07%
Fish aquatic toxicity + 0.8305 83.05%

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 94.58% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.03% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.24% 81.11%
CHEMBL2535 P11166 Glucose transporter 87.02% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.72% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.79% 85.14%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.74% 97.21%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.93% 97.36%
CHEMBL340 P08684 Cytochrome P450 3A4 81.91% 91.19%
CHEMBL2581 P07339 Cathepsin D 81.67% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 81.54% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.30% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.26% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.81% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.36% 94.00%

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.
Hofmeisteria schaffneri

Cross-Links

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PubChem 9167405
LOTUS LTS0176855
wikiData Q82242388