2,4,6-Trimethoxybenzoic acid

Details

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Internal ID 2ed41c7a-bd91-47ba-bda2-576dd8fdb6a2
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > P-methoxybenzoic acids and derivatives
IUPAC Name 2,4,6-trimethoxybenzoic acid
SMILES (Canonical) COC1=CC(=C(C(=C1)OC)C(=O)O)OC
SMILES (Isomeric) COC1=CC(=C(C(=C1)OC)C(=O)O)OC
InChI InChI=1S/C10H12O5/c1-13-6-4-7(14-2)9(10(11)12)8(5-6)15-3/h4-5H,1-3H3,(H,11,12)
InChI Key JATAKEDDMQNPOQ-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O5
Molecular Weight 212.20 g/mol
Exact Mass 212.06847348 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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570-02-5
Benzoic acid, 2,4,6-trimethoxy-
MFCD00016497
EINECS 209-325-4
SCHEMBL466144
DTXSID1060348
AKOS009148700
CS-W021498
AS-32992
SY017902
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4,6-Trimethoxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9870 98.70%
Caco-2 + 0.5706 57.06%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.9054 90.54%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9585 95.85%
OATP1B3 inhibitior + 0.9637 96.37%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9366 93.66%
P-glycoprotein inhibitior - 0.9304 93.04%
P-glycoprotein substrate - 0.9828 98.28%
CYP3A4 substrate - 0.7416 74.16%
CYP2C9 substrate - 0.7791 77.91%
CYP2D6 substrate - 0.8626 86.26%
CYP3A4 inhibition - 0.9331 93.31%
CYP2C9 inhibition - 0.9885 98.85%
CYP2C19 inhibition - 0.9411 94.11%
CYP2D6 inhibition - 0.9658 96.58%
CYP1A2 inhibition - 0.8835 88.35%
CYP2C8 inhibition - 0.8488 84.88%
CYP inhibitory promiscuity - 0.8903 89.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6330 63.30%
Carcinogenicity (trinary) Non-required 0.7239 72.39%
Eye corrosion - 0.5846 58.46%
Eye irritation + 0.9417 94.17%
Skin irritation + 0.4940 49.40%
Skin corrosion - 0.9845 98.45%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7990 79.90%
Micronuclear - 0.5293 52.93%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9445 94.45%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity + 0.7725 77.25%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6388 63.88%
Acute Oral Toxicity (c) II 0.7308 73.08%
Estrogen receptor binding - 0.6201 62.01%
Androgen receptor binding - 0.7139 71.39%
Thyroid receptor binding - 0.6036 60.36%
Glucocorticoid receptor binding - 0.8116 81.16%
Aromatase binding + 0.5445 54.45%
PPAR gamma + 0.5623 56.23%
Honey bee toxicity - 0.9712 97.12%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9328 93.28%

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 95.41% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.34% 95.56%
CHEMBL4208 P20618 Proteasome component C5 88.44% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.64% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.61% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.51% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 83.88% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.86% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.49% 91.11%
CHEMBL2535 P11166 Glucose transporter 81.34% 98.75%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.18% 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.
Vochysia thyrsoidea

Cross-Links

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PubChem 68441
LOTUS LTS0043411
wikiData Q72513706