8-Hydroxy-6-methoxy-1-methyl-9-oxoxanthene-3-sulfonic acid

Details

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Internal ID 08950122-28dc-4934-b8d8-879d73a67449
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 8-hydroxy-6-methoxy-1-methyl-9-oxoxanthene-3-sulfonic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O7S/c1-7-3-9(23(18,19)20)6-12-13(7)15(17)14-10(16)4-8(21-2)5-11(14)22-12/h3-6,16H,1-2H3,(H,18,19,20)
InChI Key YRLITUDUGDCVES-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O7S
Molecular Weight 336.30 g/mol
Exact Mass 336.03037389 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Hydroxy-6-methoxy-1-methyl-9-oxoxanthene-3-sulfonic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9031 90.31%
Caco-2 + 0.6466 64.66%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.3508 35.08%
OATP2B1 inhibitior - 0.7125 71.25%
OATP1B1 inhibitior + 0.9256 92.56%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6764 67.64%
P-glycoprotein inhibitior - 0.7754 77.54%
P-glycoprotein substrate - 0.8431 84.31%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6192 61.92%
CYP2D6 substrate - 0.8613 86.13%
CYP3A4 inhibition - 0.6488 64.88%
CYP2C9 inhibition - 0.7516 75.16%
CYP2C19 inhibition - 0.7656 76.56%
CYP2D6 inhibition - 0.8776 87.76%
CYP1A2 inhibition - 0.5759 57.59%
CYP2C8 inhibition - 0.6810 68.10%
CYP inhibitory promiscuity - 0.6815 68.15%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.7255 72.55%
Carcinogenicity (trinary) Non-required 0.6009 60.09%
Eye corrosion - 0.7620 76.20%
Eye irritation + 0.6532 65.32%
Skin irritation - 0.7706 77.06%
Skin corrosion - 0.8707 87.07%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7901 79.01%
Micronuclear + 0.9400 94.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8873 88.73%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7583 75.83%
Acute Oral Toxicity (c) III 0.6691 66.91%
Estrogen receptor binding - 0.6494 64.94%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.7981 79.81%
Glucocorticoid receptor binding - 0.6215 62.15%
Aromatase binding - 0.6123 61.23%
PPAR gamma + 0.6267 62.67%
Honey bee toxicity - 0.8800 88.00%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9745 97.45%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.54% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.82% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.37% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 91.62% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 90.44% 93.65%
CHEMBL2581 P07339 Cathepsin D 90.31% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.59% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.33% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.52% 99.15%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.86% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.78% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.55% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.93% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.49% 86.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.25% 93.40%

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 129882341
LOTUS LTS0196704
wikiData Q105352862