1-Hydroxy-3,5-dimethoxy-xanthen-9-one

Details

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Internal ID 9529730c-6c38-48d5-986a-79ae398e6ec1
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-hydroxy-3,5-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC=CC2=C1OC3=CC(=CC(=C3C2=O)O)OC
SMILES (Isomeric) COC1=CC=CC2=C1OC3=CC(=CC(=C3C2=O)O)OC
InChI InChI=1S/C15H12O5/c1-18-8-6-10(16)13-12(7-8)20-15-9(14(13)17)4-3-5-11(15)19-2/h3-7,16H,1-2H3
InChI Key IVNMXDMMZVLIRJ-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O5
Molecular Weight 272.25 g/mol
Exact Mass 272.06847348 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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1-Hydroxy-3,5-dimethoxy-xanthen-9-one
SCHEMBL7931361
1-hydroxy-3,5-dimethoxyxanthone
BDBM50155421
3,5-Dimethoxy-1-dihydroxyxanthen-9-one

2D Structure

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2D Structure of 1-Hydroxy-3,5-dimethoxy-xanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9801 98.01%
Caco-2 + 0.7442 74.42%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6570 65.70%
OATP2B1 inhibitior - 0.7242 72.42%
OATP1B1 inhibitior + 0.9371 93.71%
OATP1B3 inhibitior + 0.9768 97.68%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.4891 48.91%
P-glycoprotein inhibitior + 0.6191 61.91%
P-glycoprotein substrate - 0.8373 83.73%
CYP3A4 substrate + 0.5802 58.02%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.7032 70.32%
CYP2C9 inhibition - 0.8711 87.11%
CYP2C19 inhibition + 0.5722 57.22%
CYP2D6 inhibition - 0.7639 76.39%
CYP1A2 inhibition + 0.9175 91.75%
CYP2C8 inhibition + 0.5467 54.67%
CYP inhibitory promiscuity - 0.5932 59.32%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5623 56.23%
Eye corrosion - 0.9316 93.16%
Eye irritation + 0.9074 90.74%
Skin irritation - 0.6176 61.76%
Skin corrosion - 0.9870 98.70%
Ames mutagenesis + 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6088 60.88%
Micronuclear + 0.8800 88.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.9197 91.97%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6267 62.67%
Acute Oral Toxicity (c) III 0.6982 69.82%
Estrogen receptor binding + 0.8600 86.00%
Androgen receptor binding + 0.8277 82.77%
Thyroid receptor binding + 0.6967 69.67%
Glucocorticoid receptor binding + 0.8632 86.32%
Aromatase binding + 0.7908 79.08%
PPAR gamma + 0.8354 83.54%
Honey bee toxicity - 0.9089 90.89%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.6910 69.10%

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 98.01% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.80% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.65% 94.00%
CHEMBL2535 P11166 Glucose transporter 94.25% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.10% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.05% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.50% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.43% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.39% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.19% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.31% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.89% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.98% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.50% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.32% 94.45%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.79% 93.65%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.05% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 81.96% 93.31%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.73% 94.03%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.00% 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.
Canscora alata
Chironia krebsii
Frasera albomarginata
Haploclathra paniculata
Swertia calycina
Swertia chirayta
Swertia hookeri

Cross-Links

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PubChem 5479773
LOTUS LTS0197607
wikiData Q105121146