1,5-Dihydroxy-2-methoxyxanthone

Details

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Internal ID 9efcbb99-ab98-4498-8ed7-d6702b172a9c
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,5-dihydroxy-2-methoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1)OC3=C(C2=O)C=CC=C3O)O
SMILES (Isomeric) COC1=C(C2=C(C=C1)OC3=C(C2=O)C=CC=C3O)O
InChI InChI=1S/C14H10O5/c1-18-10-6-5-9-11(13(10)17)12(16)7-3-2-4-8(15)14(7)19-9/h2-6,15,17H,1H3
InChI Key IWDZOJJDTFMEHP-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O5
Molecular Weight 258.23 g/mol
Exact Mass 258.05282342 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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IWDZOJJDTFMEHP-UHFFFAOYSA-N
1,5-Dihydroxy-2-methoxy-9H-xanthen-9-one #

2D Structure

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2D Structure of 1,5-Dihydroxy-2-methoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.6395 63.95%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7377 73.77%
OATP2B1 inhibitior - 0.7058 70.58%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9934 99.34%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7079 70.79%
P-glycoprotein inhibitior - 0.7127 71.27%
P-glycoprotein substrate - 0.8613 86.13%
CYP3A4 substrate + 0.5468 54.68%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7181 71.81%
CYP2C9 inhibition - 0.5805 58.05%
CYP2C19 inhibition + 0.7909 79.09%
CYP2D6 inhibition - 0.7438 74.38%
CYP1A2 inhibition + 0.9811 98.11%
CYP2C8 inhibition - 0.5875 58.75%
CYP inhibitory promiscuity + 0.6572 65.72%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5675 56.75%
Eye corrosion - 0.9577 95.77%
Eye irritation + 0.8568 85.68%
Skin irritation - 0.5200 52.00%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7546 75.46%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9205 92.05%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.7863 78.63%
Acute Oral Toxicity (c) III 0.8197 81.97%
Estrogen receptor binding + 0.8157 81.57%
Androgen receptor binding + 0.6796 67.96%
Thyroid receptor binding + 0.5689 56.89%
Glucocorticoid receptor binding + 0.8887 88.87%
Aromatase binding + 0.8108 81.08%
PPAR gamma + 0.8019 80.19%
Honey bee toxicity - 0.9047 90.47%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.8258 82.58%

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 96.74% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.99% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.98% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.56% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.79% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.15% 89.00%
CHEMBL2581 P07339 Cathepsin D 91.25% 98.95%
CHEMBL2535 P11166 Glucose transporter 89.18% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 88.59% 90.20%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.51% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.21% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.02% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 84.78% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.65% 85.14%
CHEMBL1937 Q92769 Histone deacetylase 2 83.05% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.94% 95.89%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.55% 98.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.45% 95.50%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.30% 93.65%

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.
Hypericum beanii
Hypericum sampsonii

Cross-Links

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PubChem 5377509
LOTUS LTS0099329
wikiData Q105121536