4-(3,4-Dimethoxyphenoxy)benzene-1,3-dicarboxylic acid

Details

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Internal ID 7f90a577-dd7b-4281-a8ca-3f7e1a21633b
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name 4-(3,4-dimethoxyphenoxy)benzene-1,3-dicarboxylic acid
SMILES (Canonical) COC1=C(C=C(C=C1)OC2=C(C=C(C=C2)C(=O)O)C(=O)O)OC
SMILES (Isomeric) COC1=C(C=C(C=C1)OC2=C(C=C(C=C2)C(=O)O)C(=O)O)OC
InChI InChI=1S/C16H14O7/c1-21-13-6-4-10(8-14(13)22-2)23-12-5-3-9(15(17)18)7-11(12)16(19)20/h3-8H,1-2H3,(H,17,18)(H,19,20)
InChI Key RCQOZFFMJIPBHR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H14O7
Molecular Weight 318.28 g/mol
Exact Mass 318.07395278 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(3,4-Dimethoxyphenoxy)benzene-1,3-dicarboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9612 96.12%
Caco-2 + 0.8089 80.89%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.8861 88.61%
OATP2B1 inhibitior - 0.7205 72.05%
OATP1B1 inhibitior + 0.9557 95.57%
OATP1B3 inhibitior + 0.8152 81.52%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5625 56.25%
P-glycoprotein inhibitior - 0.6889 68.89%
P-glycoprotein substrate - 0.9380 93.80%
CYP3A4 substrate - 0.6580 65.80%
CYP2C9 substrate - 0.7828 78.28%
CYP2D6 substrate - 0.8619 86.19%
CYP3A4 inhibition - 0.9470 94.70%
CYP2C9 inhibition - 0.7162 71.62%
CYP2C19 inhibition - 0.8283 82.83%
CYP2D6 inhibition - 0.8713 87.13%
CYP1A2 inhibition - 0.5924 59.24%
CYP2C8 inhibition + 0.7229 72.29%
CYP inhibitory promiscuity - 0.8161 81.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7228 72.28%
Carcinogenicity (trinary) Non-required 0.6870 68.70%
Eye corrosion - 0.9718 97.18%
Eye irritation + 0.6988 69.88%
Skin irritation - 0.7219 72.19%
Skin corrosion - 0.9451 94.51%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8182 81.82%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5969 59.69%
skin sensitisation - 0.9400 94.00%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.7164 71.64%
Acute Oral Toxicity (c) II 0.4350 43.50%
Estrogen receptor binding + 0.8104 81.04%
Androgen receptor binding + 0.5427 54.27%
Thyroid receptor binding + 0.7122 71.22%
Glucocorticoid receptor binding + 0.8632 86.32%
Aromatase binding + 0.7364 73.64%
PPAR gamma + 0.6242 62.42%
Honey bee toxicity - 0.9672 96.72%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9856 98.56%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.28% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.52% 99.17%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.48% 87.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.31% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 91.84% 90.20%
CHEMBL2535 P11166 Glucose transporter 91.81% 98.75%
CHEMBL4208 P20618 Proteasome component C5 91.62% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.24% 96.09%
CHEMBL3194 P02766 Transthyretin 90.23% 90.71%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.91% 81.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.32% 94.42%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.63% 93.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.98% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 84.13% 93.31%
CHEMBL1811 P34995 Prostanoid EP1 receptor 81.87% 95.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.18% 95.50%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 80.94% 96.47%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 80.40% 89.23%

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.
Pinus mugo

Cross-Links

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PubChem 12439807
LOTUS LTS0231771
wikiData Q105233877