2-((2-Hydroxybenzoyl)amino)-4-methoxybenzoic acid

Details

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Internal ID c54cb880-03f7-4a67-8c7c-6e4870c2ee84
Taxonomy Benzenoids > Benzene and substituted derivatives > Anilides > Aromatic anilides > Benzanilides
IUPAC Name 2-[(2-hydroxybenzoyl)amino]-4-methoxybenzoic acid
SMILES (Canonical) COC1=CC(=C(C=C1)C(=O)O)NC(=O)C2=CC=CC=C2O
SMILES (Isomeric) COC1=CC(=C(C=C1)C(=O)O)NC(=O)C2=CC=CC=C2O
InChI InChI=1S/C15H13NO5/c1-21-9-6-7-10(15(19)20)12(8-9)16-14(18)11-4-2-3-5-13(11)17/h2-8,17H,1H3,(H,16,18)(H,19,20)
InChI Key CMFFISYKULRPFB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H13NO5
Molecular Weight 287.27 g/mol
Exact Mass 287.07937252 g/mol
Topological Polar Surface Area (TPSA) 95.90 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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93289-90-8
DTXSID90239367

2D Structure

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2D Structure of 2-((2-Hydroxybenzoyl)amino)-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 + 0.8022 80.22%
Caco-2 + 0.7888 78.88%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.7831 78.31%
OATP2B1 inhibitior - 0.7157 71.57%
OATP1B1 inhibitior + 0.9537 95.37%
OATP1B3 inhibitior + 0.9422 94.22%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6609 66.09%
P-glycoprotein inhibitior - 0.8418 84.18%
P-glycoprotein substrate - 0.8705 87.05%
CYP3A4 substrate - 0.6231 62.31%
CYP2C9 substrate - 0.8113 81.13%
CYP2D6 substrate - 0.8713 87.13%
CYP3A4 inhibition - 0.9160 91.60%
CYP2C9 inhibition - 0.8644 86.44%
CYP2C19 inhibition - 0.9273 92.73%
CYP2D6 inhibition - 0.9360 93.60%
CYP1A2 inhibition - 0.8022 80.22%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.8140 81.40%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7025 70.25%
Carcinogenicity (trinary) Non-required 0.6350 63.50%
Eye corrosion - 0.9950 99.50%
Eye irritation + 0.8693 86.93%
Skin irritation - 0.8750 87.50%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8414 84.14%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.9587 95.87%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6742 67.42%
Acute Oral Toxicity (c) III 0.7557 75.57%
Estrogen receptor binding + 0.9259 92.59%
Androgen receptor binding + 0.7593 75.93%
Thyroid receptor binding + 0.5389 53.89%
Glucocorticoid receptor binding + 0.6944 69.44%
Aromatase binding + 0.6953 69.53%
PPAR gamma + 0.6927 69.27%
Honey bee toxicity - 0.9276 92.76%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.9511 95.11%

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 99.13% 87.67%
CHEMBL3714130 P46095 G-protein coupled receptor 6 98.67% 97.36%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 97.85% 81.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.68% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.40% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.65% 96.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 90.43% 91.07%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.33% 99.15%
CHEMBL2535 P11166 Glucose transporter 90.29% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.83% 95.50%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 87.14% 96.47%
CHEMBL2581 P07339 Cathepsin D 86.77% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.48% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.41% 94.42%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.26% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.92% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.88% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.86% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.24% 91.19%
CHEMBL221 P23219 Cyclooxygenase-1 81.15% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.46% 85.14%

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 179711
LOTUS LTS0118254
wikiData Q83121715