4-Hydroxy-2,5-dimethoxybenzoic acid

Details

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Internal ID 61417968-23c8-4fda-8c95-e85943f41285
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > O-methoxybenzoic acids and derivatives
IUPAC Name 4-hydroxy-2,5-dimethoxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H10O5/c1-13-7-4-6(10)8(14-2)3-5(7)9(11)12/h3-4,10H,1-2H3,(H,11,12)
InChI Key USWQSWPPLTXILD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O5
Molecular Weight 198.17 g/mol
Exact Mass 198.05282342 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.11
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-2,5-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 + 0.9697 96.97%
Caco-2 + 0.6750 67.50%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.8825 88.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9400 94.00%
OATP1B3 inhibitior + 0.9636 96.36%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9492 94.92%
P-glycoprotein inhibitior - 0.9402 94.02%
P-glycoprotein substrate - 0.9825 98.25%
CYP3A4 substrate - 0.7652 76.52%
CYP2C9 substrate - 0.7957 79.57%
CYP2D6 substrate - 0.8545 85.45%
CYP3A4 inhibition - 0.9538 95.38%
CYP2C9 inhibition - 0.9316 93.16%
CYP2C19 inhibition - 0.8579 85.79%
CYP2D6 inhibition - 0.9445 94.45%
CYP1A2 inhibition - 0.9052 90.52%
CYP2C8 inhibition - 0.8809 88.09%
CYP inhibitory promiscuity - 0.8767 87.67%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.7009 70.09%
Carcinogenicity (trinary) Non-required 0.7159 71.59%
Eye corrosion + 0.5056 50.56%
Eye irritation + 0.9953 99.53%
Skin irritation + 0.6720 67.20%
Skin corrosion - 0.9348 93.48%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6899 68.99%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8184 81.84%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) II 0.4765 47.65%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.8940 89.40%
Thyroid receptor binding - 0.7450 74.50%
Glucocorticoid receptor binding - 0.6404 64.04%
Aromatase binding - 0.7795 77.95%
PPAR gamma - 0.7580 75.80%
Honey bee toxicity - 0.9591 95.91%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.9061 90.61%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.67% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.96% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.59% 95.56%
CHEMBL3194 P02766 Transthyretin 89.84% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.50% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.04% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.17% 99.17%
CHEMBL2535 P11166 Glucose transporter 86.86% 98.75%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.59% 94.42%
CHEMBL2581 P07339 Cathepsin D 82.86% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 82.66% 90.20%
CHEMBL4208 P20618 Proteasome component C5 82.53% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.82% 99.15%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.39% 81.11%
CHEMBL1811 P34995 Prostanoid EP1 receptor 80.53% 95.71%

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.
Tagetes minuta

Cross-Links

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PubChem 85773933
LOTUS LTS0054796
wikiData Q105278548