Pestaloxanthone

Details

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Internal ID 374645c2-7373-4fe4-8b34-3ed5a45b5f6c
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 8-hydroxy-6-(hydroxymethyl)-3-methoxy-9-oxoxanthene-1-carboxylate
SMILES (Canonical) COC1=CC(=C2C(=C1)OC3=CC(=CC(=C3C2=O)O)CO)C(=O)OC
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC3=CC(=CC(=C3C2=O)O)CO)C(=O)OC
InChI InChI=1S/C17H14O7/c1-22-9-5-10(17(21)23-2)14-13(6-9)24-12-4-8(7-18)3-11(19)15(12)16(14)20/h3-6,18-19H,7H2,1-2H3
InChI Key IJUFSGBZRCCKSS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O7
Molecular Weight 330.29 g/mol
Exact Mass 330.07395278 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 7
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 Pestaloxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8427 84.27%
Caco-2 + 0.6852 68.52%
Blood Brain Barrier - 0.9500 95.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7484 74.84%
OATP2B1 inhibitior - 0.5736 57.36%
OATP1B1 inhibitior + 0.8161 81.61%
OATP1B3 inhibitior + 0.9303 93.03%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5173 51.73%
P-glycoprotein inhibitior - 0.5922 59.22%
P-glycoprotein substrate - 0.7787 77.87%
CYP3A4 substrate + 0.5359 53.59%
CYP2C9 substrate - 0.5942 59.42%
CYP2D6 substrate - 0.8549 85.49%
CYP3A4 inhibition - 0.7357 73.57%
CYP2C9 inhibition + 0.5537 55.37%
CYP2C19 inhibition - 0.7113 71.13%
CYP2D6 inhibition - 0.8255 82.55%
CYP1A2 inhibition - 0.6600 66.00%
CYP2C8 inhibition + 0.4464 44.64%
CYP inhibitory promiscuity - 0.5446 54.46%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9113 91.13%
Carcinogenicity (trinary) Non-required 0.6836 68.36%
Eye corrosion - 0.9686 96.86%
Eye irritation + 0.6931 69.31%
Skin irritation - 0.8330 83.30%
Skin corrosion - 0.9759 97.59%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6276 62.76%
Micronuclear + 0.6874 68.74%
Hepatotoxicity - 0.5435 54.35%
skin sensitisation - 0.9489 94.89%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6701 67.01%
Acute Oral Toxicity (c) III 0.5898 58.98%
Estrogen receptor binding + 0.8218 82.18%
Androgen receptor binding + 0.7154 71.54%
Thyroid receptor binding - 0.6550 65.50%
Glucocorticoid receptor binding + 0.8780 87.80%
Aromatase binding + 0.7731 77.31%
PPAR gamma + 0.7888 78.88%
Honey bee toxicity - 0.8952 89.52%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.8273 82.73%

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 97.99% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.02% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.92% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.51% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.31% 99.17%
CHEMBL4208 P20618 Proteasome component C5 88.42% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 88.06% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.74% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.92% 93.99%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.50% 94.42%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.32% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.37% 95.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.89% 96.95%
CHEMBL2535 P11166 Glucose transporter 84.68% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.00% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.20% 99.15%
CHEMBL340 P08684 Cytochrome P450 3A4 80.93% 91.19%

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 57342265
LOTUS LTS0136212
wikiData Q77279109