Pestalotether A

Details

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Internal ID d82ec993-9b64-4bbd-87c9-ee5baa689d31
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name methyl 4-chloro-3-hydroxy-2-(3-hydroxy-2-methoxycarbonyl-5-methylphenoxy)-5-methoxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H17ClO8/c1-8-5-10(20)13(18(23)26-4)11(6-8)27-16-9(17(22)25-3)7-12(24-2)14(19)15(16)21/h5-7,20-21H,1-4H3
InChI Key UNYKCSQBZSEKRS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H17ClO8
Molecular Weight 396.80 g/mol
Exact Mass 396.0611952 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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methyl 4-chloro-3-hydroxy-2-(3-hydroxy-2-methoxycarbonyl-5-methyl-phenoxy)-5-methoxy-benzoate

2D Structure

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2D Structure of Pestalotether A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9690 96.90%
Caco-2 + 0.7932 79.32%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.8602 86.02%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.8353 83.53%
OATP1B3 inhibitior - 0.3786 37.86%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8226 82.26%
P-glycoprotein inhibitior - 0.5488 54.88%
P-glycoprotein substrate - 0.8663 86.63%
CYP3A4 substrate + 0.5642 56.42%
CYP2C9 substrate - 0.8162 81.62%
CYP2D6 substrate - 0.8609 86.09%
CYP3A4 inhibition - 0.9470 94.70%
CYP2C9 inhibition - 0.7881 78.81%
CYP2C19 inhibition - 0.7514 75.14%
CYP2D6 inhibition - 0.8915 89.15%
CYP1A2 inhibition - 0.5569 55.69%
CYP2C8 inhibition + 0.7417 74.17%
CYP inhibitory promiscuity - 0.7667 76.67%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6257 62.57%
Carcinogenicity (trinary) Non-required 0.4484 44.84%
Eye corrosion - 0.9828 98.28%
Eye irritation - 0.6160 61.60%
Skin irritation - 0.7218 72.18%
Skin corrosion - 0.9402 94.02%
Ames mutagenesis - 0.5937 59.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4659 46.59%
Micronuclear + 0.6374 63.74%
Hepatotoxicity + 0.6773 67.73%
skin sensitisation - 0.8781 87.81%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5607 56.07%
Acute Oral Toxicity (c) III 0.5235 52.35%
Estrogen receptor binding + 0.8352 83.52%
Androgen receptor binding - 0.4891 48.91%
Thyroid receptor binding + 0.6320 63.20%
Glucocorticoid receptor binding + 0.7410 74.10%
Aromatase binding + 0.5237 52.37%
PPAR gamma + 0.8224 82.24%
Honey bee toxicity - 0.9390 93.90%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7034 70.34%
Fish aquatic toxicity + 0.9960 99.60%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.57% 91.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.59% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 91.14% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.65% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.36% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 89.27% 94.42%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.46% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.72% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.55% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.66% 99.15%
CHEMBL3194 P02766 Transthyretin 85.89% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.58% 95.56%
CHEMBL2056 P21728 Dopamine D1 receptor 83.17% 91.00%
CHEMBL4040 P28482 MAP kinase ERK2 82.53% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.51% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 82.40% 91.19%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 82.34% 92.29%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.56% 96.90%
CHEMBL2535 P11166 Glucose transporter 81.13% 98.75%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.10% 96.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.10% 91.07%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.98% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.00% 99.17%

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.
Rhizophora apiculata

Cross-Links

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PubChem 57342094
LOTUS LTS0247498
wikiData Q77492108