2-((2,4-Dihydroxybenzoyl)amino)-4-methoxybenzoic acid

Details

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Internal ID e56f6bbc-d6a7-48ca-89e8-ee2923933aca
Taxonomy Benzenoids > Benzene and substituted derivatives > Anilides > Aromatic anilides > Benzanilides
IUPAC Name 2-[(2,4-dihydroxybenzoyl)amino]-4-methoxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H13NO6/c1-22-9-3-5-10(15(20)21)12(7-9)16-14(19)11-4-2-8(17)6-13(11)18/h2-7,17-18H,1H3,(H,16,19)(H,20,21)
InChI Key GLXWWDVTVBGZGZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H13NO6
Molecular Weight 303.27 g/mol
Exact Mass 303.07428713 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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2-((2,4-Dihydroxybenzoyl)amino)-4-methoxybenzoic acid
DTXSID60151148

2D Structure

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2D Structure of 2-((2,4-Dihydroxybenzoyl)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 + 0.6898 68.98%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7831 78.31%
OATP2B1 inhibitior - 0.6987 69.87%
OATP1B1 inhibitior + 0.9455 94.55%
OATP1B3 inhibitior + 0.9422 94.22%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6780 67.80%
P-glycoprotein inhibitior - 0.8750 87.50%
P-glycoprotein substrate - 0.7835 78.35%
CYP3A4 substrate - 0.6054 60.54%
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 + 0.4665 46.65%
CYP inhibitory promiscuity - 0.8140 81.40%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7025 70.25%
Carcinogenicity (trinary) Non-required 0.6350 63.50%
Eye corrosion - 0.9950 99.50%
Eye irritation + 0.8120 81.20%
Skin irritation - 0.8750 87.50%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8856 88.56%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9587 95.87%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6536 65.36%
Acute Oral Toxicity (c) III 0.7557 75.57%
Estrogen receptor binding + 0.8888 88.88%
Androgen receptor binding + 0.8776 87.76%
Thyroid receptor binding + 0.5634 56.34%
Glucocorticoid receptor binding + 0.7901 79.01%
Aromatase binding + 0.6611 66.11%
PPAR gamma + 0.7680 76.80%
Honey bee toxicity - 0.9032 90.32%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.8200 82.00%
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
CHEMBL3714130 P46095 G-protein coupled receptor 6 98.49% 97.36%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 98.18% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 97.59% 81.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.69% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.16% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.96% 96.09%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 93.80% 94.42%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.69% 99.15%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 90.51% 91.07%
CHEMBL4208 P20618 Proteasome component C5 89.68% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.40% 99.17%
CHEMBL2535 P11166 Glucose transporter 89.39% 98.75%
CHEMBL2581 P07339 Cathepsin D 84.60% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 83.72% 91.19%
CHEMBL3194 P02766 Transthyretin 83.64% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.82% 94.45%
CHEMBL4901 P54753 Ephrin type-B receptor 3 81.81% 87.50%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.97% 95.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.84% 85.14%
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.
Dianthus caryophyllus

Cross-Links

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PubChem 189309
LOTUS LTS0136305
wikiData Q83017551