2-Benzamido-4-methoxybenzoic acid

Details

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Internal ID 6ffd63da-8752-4ccb-9f6a-12f10a9aa6e3
Taxonomy Benzenoids > Benzene and substituted derivatives > Anilides > Aromatic anilides > Benzanilides
IUPAC Name 2-benzamido-4-methoxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H13NO4/c1-20-11-7-8-12(15(18)19)13(9-11)16-14(17)10-5-3-2-4-6-10/h2-9H,1H3,(H,16,17)(H,18,19)
InChI Key NZSBJWOTLHVBNU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H13NO4
Molecular Weight 271.27 g/mol
Exact Mass 271.08445790 g/mol
Topological Polar Surface Area (TPSA) 75.60 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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N-benzoyl-4-methoxyanthranilic acid
2-(benzoylamino)-4-methoxybenzoic acid
Benzoic acid, 2-(benzoylamino)-4-methoxy-
109437-82-3
C04208
SCHEMBL2935687
CHEBI:28609
DTXSID40331481
Q27103793

2D Structure

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2D Structure of 2-Benzamido-4-methoxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7647 76.47%
Caco-2 + 0.8146 81.46%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.8225 82.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9562 95.62%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6274 62.74%
P-glycoprotein inhibitior - 0.7864 78.64%
P-glycoprotein substrate - 0.9121 91.21%
CYP3A4 substrate - 0.6689 66.89%
CYP2C9 substrate - 0.7939 79.39%
CYP2D6 substrate - 0.8754 87.54%
CYP3A4 inhibition - 0.8949 89.49%
CYP2C9 inhibition - 0.7409 74.09%
CYP2C19 inhibition - 0.9177 91.77%
CYP2D6 inhibition - 0.9572 95.72%
CYP1A2 inhibition - 0.7527 75.27%
CYP2C8 inhibition + 0.6082 60.82%
CYP inhibitory promiscuity - 0.8070 80.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7132 71.32%
Carcinogenicity (trinary) Non-required 0.5829 58.29%
Eye corrosion - 0.9951 99.51%
Eye irritation + 0.8754 87.54%
Skin irritation - 0.8757 87.57%
Skin corrosion - 0.9819 98.19%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7940 79.40%
Micronuclear + 0.7100 71.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9642 96.42%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.8021 80.21%
Acute Oral Toxicity (c) III 0.7510 75.10%
Estrogen receptor binding + 0.8918 89.18%
Androgen receptor binding + 0.8232 82.32%
Thyroid receptor binding - 0.4933 49.33%
Glucocorticoid receptor binding + 0.5841 58.41%
Aromatase binding + 0.7852 78.52%
PPAR gamma + 0.6220 62.20%
Honey bee toxicity - 0.9549 95.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9589 95.89%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 99.90% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 99.50% 81.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 96.81% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.24% 95.56%
CHEMBL2535 P11166 Glucose transporter 93.28% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.10% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.26% 86.33%
CHEMBL4208 P20618 Proteasome component C5 89.42% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 88.80% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.59% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.34% 96.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.91% 93.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.69% 99.17%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.54% 94.42%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.39% 96.00%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 85.15% 96.47%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.55% 85.14%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.62% 89.34%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.44% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.33% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 80.73% 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.
Dianthus caryophyllus

Cross-Links

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PubChem 440258
LOTUS LTS0107755
wikiData Q27103793