4-(4-Carboxy-2-methoxyphenoxy)-3,5-dimethoxybenzoic acid

Details

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Internal ID ec04272b-8486-41af-8d26-919838f7a7a7
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name 4-(4-carboxy-2-methoxyphenoxy)-3,5-dimethoxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O8/c1-22-12-6-9(16(18)19)4-5-11(12)25-15-13(23-2)7-10(17(20)21)8-14(15)24-3/h4-8H,1-3H3,(H,18,19)(H,20,21)
InChI Key QRRGNRFWUZEQAV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O8
Molecular Weight 348.30 g/mol
Exact Mass 348.08451746 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(4-Carboxy-2-methoxyphenoxy)-3,5-dimethoxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9607 96.07%
Caco-2 + 0.7521 75.21%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.8704 87.04%
OATP2B1 inhibitior - 0.7108 71.08%
OATP1B1 inhibitior + 0.9587 95.87%
OATP1B3 inhibitior - 0.4404 44.04%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6468 64.68%
P-glycoprotein inhibitior - 0.7995 79.95%
P-glycoprotein substrate - 0.9428 94.28%
CYP3A4 substrate - 0.6615 66.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8572 85.72%
CYP3A4 inhibition - 0.9359 93.59%
CYP2C9 inhibition - 0.8946 89.46%
CYP2C19 inhibition - 0.9131 91.31%
CYP2D6 inhibition - 0.8917 89.17%
CYP1A2 inhibition - 0.6426 64.26%
CYP2C8 inhibition + 0.7009 70.09%
CYP inhibitory promiscuity - 0.8360 83.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7128 71.28%
Carcinogenicity (trinary) Non-required 0.6560 65.60%
Eye corrosion - 0.9799 97.99%
Eye irritation + 0.7663 76.63%
Skin irritation - 0.8204 82.04%
Skin corrosion - 0.9699 96.99%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4875 48.75%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation - 0.9537 95.37%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.6614 66.14%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.4694 46.94%
Acute Oral Toxicity (c) II 0.5681 56.81%
Estrogen receptor binding + 0.7686 76.86%
Androgen receptor binding - 0.5252 52.52%
Thyroid receptor binding + 0.5500 55.00%
Glucocorticoid receptor binding + 0.5751 57.51%
Aromatase binding - 0.5563 55.63%
PPAR gamma + 0.6968 69.68%
Honey bee toxicity - 0.9644 96.44%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.9052 90.52%
Fish aquatic toxicity + 0.9866 98.66%

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 93.85% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 93.24% 90.20%
CHEMBL3194 P02766 Transthyretin 92.91% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.79% 99.17%
CHEMBL2535 P11166 Glucose transporter 88.13% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.70% 95.56%
CHEMBL4208 P20618 Proteasome component C5 87.60% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.44% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.05% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.66% 95.50%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.41% 94.42%

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.
Elaeagnus pungens

Cross-Links

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PubChem 162916395
LOTUS LTS0233146
wikiData Q105226575