4-(2,4-Dihydroxy-3,6-dimethylbenzoyl)oxy-2-methoxy-6-methylbenzoic acid

Details

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Internal ID 08733653-a573-43cc-961c-3cedb0ea5103
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-(2,4-dihydroxy-3,6-dimethylbenzoyl)oxy-2-methoxy-6-methylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H18O7/c1-8-5-11(7-13(24-4)14(8)17(21)22)25-18(23)15-9(2)6-12(19)10(3)16(15)20/h5-7,19-20H,1-4H3,(H,21,22)
InChI Key ITAJSGQMWYFBGD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O7
Molecular Weight 346.30 g/mol
Exact Mass 346.10525291 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2,4-Dihydroxy-3,6-dimethylbenzoyl)oxy-2-methoxy-6-methylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9450 94.50%
Caco-2 + 0.7509 75.09%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8663 86.63%
OATP2B1 inhibitior - 0.7136 71.36%
OATP1B1 inhibitior + 0.9443 94.43%
OATP1B3 inhibitior - 0.5698 56.98%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5642 56.42%
P-glycoprotein inhibitior - 0.7929 79.29%
P-glycoprotein substrate - 0.9054 90.54%
CYP3A4 substrate - 0.5183 51.83%
CYP2C9 substrate - 0.6089 60.89%
CYP2D6 substrate - 0.8933 89.33%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.7343 73.43%
CYP2C19 inhibition - 0.8817 88.17%
CYP2D6 inhibition - 0.8907 89.07%
CYP1A2 inhibition - 0.6138 61.38%
CYP2C8 inhibition + 0.4553 45.53%
CYP inhibitory promiscuity - 0.6980 69.80%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7156 71.56%
Carcinogenicity (trinary) Non-required 0.7193 71.93%
Eye corrosion - 0.9856 98.56%
Eye irritation + 0.5971 59.71%
Skin irritation - 0.8241 82.41%
Skin corrosion - 0.9491 94.91%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4665 46.65%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.5785 57.85%
skin sensitisation - 0.9583 95.83%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.6059 60.59%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6470 64.70%
Acute Oral Toxicity (c) II 0.6323 63.23%
Estrogen receptor binding + 0.8782 87.82%
Androgen receptor binding + 0.5788 57.88%
Thyroid receptor binding - 0.5183 51.83%
Glucocorticoid receptor binding + 0.5881 58.81%
Aromatase binding + 0.6730 67.30%
PPAR gamma + 0.6736 67.36%
Honey bee toxicity - 0.8539 85.39%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9878 98.78%

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
CHEMBL3194 P02766 Transthyretin 92.19% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.43% 99.15%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.95% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.32% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.92% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.19% 94.42%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.92% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.55% 86.33%
CHEMBL4208 P20618 Proteasome component C5 85.27% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.50% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.13% 96.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 14805238
LOTUS LTS0253366
wikiData Q105119937