Xanthen-9-one, 1-hydroxy-3-methoxy-

Details

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Internal ID 657189de-97b6-4ae5-b453-de70ee738d93
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-hydroxy-3-methoxyxanthen-9-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC3=CC=CC=C3C2=O)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC3=CC=CC=C3C2=O)O
InChI InChI=1S/C14H10O4/c1-17-8-6-10(15)13-12(7-8)18-11-5-3-2-4-9(11)14(13)16/h2-7,15H,1H3
InChI Key OLCQJTHIMNTNQW-UHFFFAOYSA-N
Popularity 6 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 3.10
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL188014
18799-43-4
1-Hydroxy-3-methoxyxanthone
1-hydroxy-3-methoxy-xanthen-9-one
1-hydroxy-3-methoxy-9H-xanthen-9-one
DTXSID30172128
BDBM50155443

2D Structure

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2D Structure of Xanthen-9-one, 1-hydroxy-3-methoxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.8771 87.71%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6618 66.18%
OATP2B1 inhibitior - 0.8621 86.21%
OATP1B1 inhibitior + 0.9067 90.67%
OATP1B3 inhibitior + 1.0000 100.00%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7177 71.77%
P-glycoprotein inhibitior - 0.6515 65.15%
P-glycoprotein substrate - 0.9051 90.51%
CYP3A4 substrate + 0.5499 54.99%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.6830 68.30%
CYP2C9 inhibition - 0.5200 52.00%
CYP2C19 inhibition + 0.7424 74.24%
CYP2D6 inhibition - 0.8883 88.83%
CYP1A2 inhibition + 0.9819 98.19%
CYP2C8 inhibition - 0.5660 56.60%
CYP inhibitory promiscuity - 0.5494 54.94%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9113 91.13%
Carcinogenicity (trinary) Non-required 0.4739 47.39%
Eye corrosion - 0.8952 89.52%
Eye irritation + 0.9177 91.77%
Skin irritation - 0.5473 54.73%
Skin corrosion - 0.9880 98.80%
Ames mutagenesis + 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7422 74.22%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.9621 96.21%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6010 60.10%
Acute Oral Toxicity (c) III 0.8897 88.97%
Estrogen receptor binding + 0.8323 83.23%
Androgen receptor binding + 0.8852 88.52%
Thyroid receptor binding + 0.7149 71.49%
Glucocorticoid receptor binding + 0.9197 91.97%
Aromatase binding + 0.8873 88.73%
PPAR gamma + 0.8158 81.58%
Honey bee toxicity - 0.9201 92.01%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.7062 70.62%

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 98.95% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.41% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.03% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.15% 93.99%
CHEMBL2581 P07339 Cathepsin D 92.45% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.89% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.88% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.88% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.79% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 89.70% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.24% 93.65%
CHEMBL2535 P11166 Glucose transporter 89.07% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.07% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.20% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.49% 99.17%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.80% 92.67%
CHEMBL4208 P20618 Proteasome component C5 82.29% 90.00%

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 5491377
LOTUS LTS0138853
wikiData Q83042271