2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide

Details

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Internal ID b4697a76-85d8-4b00-a191-dd3465ce02e7
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylacetamides
IUPAC Name 2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide
SMILES (Canonical) CNC(=O)C(=O)C1=CC=C(C=C1)OC
SMILES (Isomeric) CNC(=O)C(=O)C1=CC=C(C=C1)OC
InChI InChI=1S/C10H11NO3/c1-11-10(13)9(12)7-3-5-8(14-2)6-4-7/h3-6H,1-2H3,(H,11,13)
InChI Key LFRNOQWLRGQVQN-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H11NO3
Molecular Weight 193.20 g/mol
Exact Mass 193.07389321 g/mol
Topological Polar Surface Area (TPSA) 55.40 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.62
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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244264-57-1
SCHEMBL4710619
LFRNOQWLRGQVQN-UHFFFAOYSA-N
2-(4-methoxy-phenyl)-N-methyl-2-oxo-acetamide
EN300-8611264

2D Structure

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2D Structure of 2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8924 89.24%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8361 83.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9588 95.88%
OATP1B3 inhibitior + 0.9628 96.28%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8815 88.15%
P-glycoprotein inhibitior - 0.9715 97.15%
P-glycoprotein substrate - 0.9535 95.35%
CYP3A4 substrate - 0.6019 60.19%
CYP2C9 substrate - 0.7865 78.65%
CYP2D6 substrate - 0.7943 79.43%
CYP3A4 inhibition - 0.9691 96.91%
CYP2C9 inhibition - 0.9617 96.17%
CYP2C19 inhibition - 0.9735 97.35%
CYP2D6 inhibition - 0.9730 97.30%
CYP1A2 inhibition - 0.6214 62.14%
CYP2C8 inhibition - 0.7894 78.94%
CYP inhibitory promiscuity - 0.9017 90.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7936 79.36%
Carcinogenicity (trinary) Non-required 0.5314 53.14%
Eye corrosion - 0.9611 96.11%
Eye irritation + 0.9313 93.13%
Skin irritation - 0.7625 76.25%
Skin corrosion - 0.9798 97.98%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6853 68.53%
Micronuclear + 0.7100 71.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.9637 96.37%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.5782 57.82%
Acute Oral Toxicity (c) III 0.8545 85.45%
Estrogen receptor binding - 0.7320 73.20%
Androgen receptor binding + 0.6820 68.20%
Thyroid receptor binding - 0.6698 66.98%
Glucocorticoid receptor binding - 0.8033 80.33%
Aromatase binding + 0.6530 65.30%
PPAR gamma - 0.9126 91.26%
Honey bee toxicity - 0.9343 93.43%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.6337 63.37%

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
CHEMBL4208 P20618 Proteasome component C5 95.99% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.16% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.99% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 86.52% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.45% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.26% 99.17%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.67% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.62% 81.11%
CHEMBL2535 P11166 Glucose transporter 83.61% 98.75%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.20% 90.24%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.11% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.34% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.36% 95.50%

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 21776239
LOTUS LTS0221345
wikiData Q105151143