8-hydroxy-3-hydroxymethyl-9-oxo-9H-xanthene-1-carboxylic acid methyl ester

Details

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Internal ID 353485e9-da54-4f66-ad48-fec382d3da0e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 8-hydroxy-3-(hydroxymethyl)-9-oxoxanthene-1-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H12O6/c1-21-16(20)9-5-8(7-17)6-12-13(9)15(19)14-10(18)3-2-4-11(14)22-12/h2-6,17-18H,7H2,1H3
InChI Key VQOGZZUCGPWKHD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O6
Molecular Weight 300.26 g/mol
Exact Mass 300.06338810 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.93
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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RefChem:107133
CHEBI:217496
methyl 8-hydroxy-3-(hydroxymethyl)-9-oxoxanthene-1-carboxylate

2D Structure

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2D Structure of 8-hydroxy-3-hydroxymethyl-9-oxo-9H-xanthene-1-carboxylic acid methyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9404 94.04%
Caco-2 + 0.5570 55.70%
Blood Brain Barrier - 0.9500 95.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7523 75.23%
OATP2B1 inhibitior - 0.5780 57.80%
OATP1B1 inhibitior + 0.8218 82.18%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5413 54.13%
P-glycoprotein inhibitior - 0.6876 68.76%
P-glycoprotein substrate - 0.7229 72.29%
CYP3A4 substrate + 0.5399 53.99%
CYP2C9 substrate - 0.5744 57.44%
CYP2D6 substrate - 0.8685 86.85%
CYP3A4 inhibition - 0.8178 81.78%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition - 0.6930 69.30%
CYP2D6 inhibition - 0.9063 90.63%
CYP1A2 inhibition - 0.5816 58.16%
CYP2C8 inhibition + 0.6137 61.37%
CYP inhibitory promiscuity - 0.6359 63.59%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9013 90.13%
Carcinogenicity (trinary) Non-required 0.6169 61.69%
Eye corrosion - 0.9427 94.27%
Eye irritation + 0.6749 67.49%
Skin irritation - 0.8027 80.27%
Skin corrosion - 0.9764 97.64%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7287 72.87%
Micronuclear + 0.7074 70.74%
Hepatotoxicity - 0.5507 55.07%
skin sensitisation - 0.9525 95.25%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.5761 57.61%
Acute Oral Toxicity (c) III 0.7752 77.52%
Estrogen receptor binding + 0.8182 81.82%
Androgen receptor binding + 0.7438 74.38%
Thyroid receptor binding - 0.7148 71.48%
Glucocorticoid receptor binding + 0.9055 90.55%
Aromatase binding + 0.7244 72.44%
PPAR gamma + 0.7707 77.07%
Honey bee toxicity - 0.9421 94.21%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.7801 78.01%

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
CHEMBL2581 P07339 Cathepsin D 98.03% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.85% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.41% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.79% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.32% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.09% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.76% 99.17%
CHEMBL2535 P11166 Glucose transporter 88.42% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.85% 93.99%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.79% 96.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.40% 95.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.94% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.72% 95.56%

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 132504559
LOTUS LTS0096876
wikiData Q104199696