5-Hydroxy-3-methoxyxanthone

Details

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Internal ID 98171c14-24bb-42c8-b996-a96faf79ad64
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 5-hydroxy-3-methoxyxanthen-9-one
SMILES (Canonical) COC1=CC2=C(C=C1)C(=O)C3=C(O2)C(=CC=C3)O
SMILES (Isomeric) COC1=CC2=C(C=C1)C(=O)C3=C(O2)C(=CC=C3)O
InChI InChI=1S/C14H10O4/c1-17-8-5-6-9-12(7-8)18-14-10(13(9)16)3-2-4-11(14)15/h2-7,15H,1H3
InChI Key IGEOTHJTYYISJW-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O4
Molecular Weight 242.23 g/mol
Exact Mass 242.05790880 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL4543469

2D Structure

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2D Structure of 5-Hydroxy-3-methoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9846 98.46%
Caco-2 + 0.7773 77.73%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.6551 65.51%
OATP2B1 inhibitior - 0.7251 72.51%
OATP1B1 inhibitior + 0.9624 96.24%
OATP1B3 inhibitior + 0.9952 99.52%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7469 74.69%
P-glycoprotein inhibitior - 0.6545 65.45%
P-glycoprotein substrate - 0.8812 88.12%
CYP3A4 substrate + 0.5480 54.80%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition + 0.5981 59.81%
CYP2C9 inhibition - 0.7716 77.16%
CYP2C19 inhibition + 0.6254 62.54%
CYP2D6 inhibition - 0.8637 86.37%
CYP1A2 inhibition + 0.9667 96.67%
CYP2C8 inhibition - 0.6531 65.31%
CYP inhibitory promiscuity - 0.5933 59.33%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4627 46.27%
Eye corrosion - 0.8980 89.80%
Eye irritation + 0.9069 90.69%
Skin irritation - 0.5327 53.27%
Skin corrosion - 0.9840 98.40%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8040 80.40%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.6652 66.52%
skin sensitisation - 0.9316 93.16%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7417 74.17%
Acute Oral Toxicity (c) III 0.9193 91.93%
Estrogen receptor binding + 0.8583 85.83%
Androgen receptor binding + 0.8853 88.53%
Thyroid receptor binding + 0.6790 67.90%
Glucocorticoid receptor binding + 0.9340 93.40%
Aromatase binding + 0.8768 87.68%
PPAR gamma + 0.8448 84.48%
Honey bee toxicity - 0.9126 91.26%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.6426 64.26%

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 99.27% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.76% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.91% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.03% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.47% 99.15%
CHEMBL1907 P15144 Aminopeptidase N 93.13% 93.31%
CHEMBL2581 P07339 Cathepsin D 92.62% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.04% 99.23%
CHEMBL2535 P11166 Glucose transporter 90.78% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.28% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 89.24% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 88.06% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.61% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.74% 94.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.49% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.10% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.72% 95.50%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.42% 93.65%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.90% 100.00%

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.
Chironia krebsii

Cross-Links

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PubChem 57490839
LOTUS LTS0225470
wikiData Q105112571