3,4-Bis(methoxycarbonyl)benzoic acid

Details

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Internal ID 24184775-e8ac-48cf-b822-121452ab43c1
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name 3,4-bis(methoxycarbonyl)benzoic acid
SMILES (Canonical) COC(=O)C1=C(C=C(C=C1)C(=O)O)C(=O)OC
SMILES (Isomeric) COC(=O)C1=C(C=C(C=C1)C(=O)O)C(=O)OC
InChI InChI=1S/C11H10O6/c1-16-10(14)7-4-3-6(9(12)13)5-8(7)11(15)17-2/h3-5H,1-2H3,(H,12,13)
InChI Key KUQGJFOIULVBKJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O6
Molecular Weight 238.19 g/mol
Exact Mass 238.04773803 g/mol
Topological Polar Surface Area (TPSA) 89.90 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.96
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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54699-35-3
1,2,4-Benzenetricarboxylic acid, 1,2-dimethyl ester
SCHEMBL820141
3,4-dicarbomethoxybenzoic acid
benzene-1,2,4-tricarboxylic acid-1,2-dimethyl ester
CHEBI:87385
KUQGJFOIULVBKJ-UHFFFAOYSA-N
DTXSID201334250
3,4-bis(methoxycarbonyl)-benzoic acid
3,4-Bis(methoxycarbonyl)benzoic acid #
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4-Bis(methoxycarbonyl)benzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9552 95.52%
Caco-2 + 0.6093 60.93%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.9179 91.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9649 96.49%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9110 91.10%
P-glycoprotein inhibitior - 0.9321 93.21%
P-glycoprotein substrate - 0.9581 95.81%
CYP3A4 substrate - 0.7437 74.37%
CYP2C9 substrate - 0.7613 76.13%
CYP2D6 substrate - 0.8917 89.17%
CYP3A4 inhibition - 0.9804 98.04%
CYP2C9 inhibition - 0.9703 97.03%
CYP2C19 inhibition - 0.9682 96.82%
CYP2D6 inhibition - 0.9475 94.75%
CYP1A2 inhibition - 0.9222 92.22%
CYP2C8 inhibition + 0.5163 51.63%
CYP inhibitory promiscuity - 0.9578 95.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5690 56.90%
Carcinogenicity (trinary) Non-required 0.7787 77.87%
Eye corrosion - 0.6552 65.52%
Eye irritation + 0.9780 97.80%
Skin irritation - 0.6114 61.14%
Skin corrosion - 0.9502 95.02%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8161 81.61%
Micronuclear - 0.7326 73.26%
Hepatotoxicity - 0.5060 50.60%
skin sensitisation - 0.6383 63.83%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6419 64.19%
Acute Oral Toxicity (c) IV 0.4915 49.15%
Estrogen receptor binding + 0.6678 66.78%
Androgen receptor binding - 0.6154 61.54%
Thyroid receptor binding - 0.7717 77.17%
Glucocorticoid receptor binding - 0.7291 72.91%
Aromatase binding - 0.6115 61.15%
PPAR gamma - 0.7799 77.99%
Honey bee toxicity - 0.9815 98.15%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.9662 96.62%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 97.28% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 95.75% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.34% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.05% 94.42%
CHEMBL4208 P20618 Proteasome component C5 85.64% 90.00%
CHEMBL2581 P07339 Cathepsin D 85.54% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.66% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.84% 99.17%
CHEMBL2535 P11166 Glucose transporter 81.58% 98.75%
CHEMBL3194 P02766 Transthyretin 80.65% 90.71%

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.
Atractylodes lancea
Atractylodes macrocephala
Cnidium monnieri
Torilis japonica

Cross-Links

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PubChem 610016
NPASS NPC65861