1,3,7-Trihydroxy-2-methoxyxanthone

Details

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Internal ID c41af041-7453-4361-bb77-4e2c08754ad1
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,7-trihydroxy-2-methoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O
SMILES (Isomeric) COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O
InChI InChI=1S/C14H10O6/c1-19-14-8(16)5-10-11(13(14)18)12(17)7-4-6(15)2-3-9(7)20-10/h2-5,15-16,18H,1H3
InChI Key GLXRAYJUKLGHEP-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O6
Molecular Weight 274.22 g/mol
Exact Mass 274.04773803 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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211948-69-5
1,3,7-TRIHYDROXY-2-METHOXYXANTHEN-9-ONE
9H-Xanthen-9-one, 1,3,7-trihydroxy-2-methoxy-
CHEMBL2436928
DTXSID20478227
1,3,7-TRIHYDROXY-2-METHOXY-9H-XANTHEN-9-ONE

2D Structure

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2D Structure of 1,3,7-Trihydroxy-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 + 0.9378 93.78%
Caco-2 + 0.8108 81.08%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5512 55.12%
OATP2B1 inhibitior - 0.6904 69.04%
OATP1B1 inhibitior + 0.8720 87.20%
OATP1B3 inhibitior + 0.9758 97.58%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8642 86.42%
P-glycoprotein inhibitior - 0.7939 79.39%
P-glycoprotein substrate - 0.8104 81.04%
CYP3A4 substrate + 0.5129 51.29%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.6321 63.21%
CYP2C9 inhibition - 0.6549 65.49%
CYP2C19 inhibition + 0.6923 69.23%
CYP2D6 inhibition - 0.6476 64.76%
CYP1A2 inhibition + 0.9724 97.24%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.7640 76.40%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6276 62.76%
Eye corrosion - 0.9630 96.30%
Eye irritation + 0.8867 88.67%
Skin irritation - 0.5358 53.58%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7422 74.22%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8858 88.58%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.9024 90.24%
Acute Oral Toxicity (c) III 0.7996 79.96%
Estrogen receptor binding + 0.7447 74.47%
Androgen receptor binding + 0.7914 79.14%
Thyroid receptor binding + 0.5761 57.61%
Glucocorticoid receptor binding + 0.8922 89.22%
Aromatase binding + 0.7895 78.95%
PPAR gamma + 0.7749 77.49%
Honey bee toxicity - 0.8686 86.86%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.7882 78.82%

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 98.60% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.86% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.85% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.68% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.59% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.80% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.95% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.76% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.44% 85.14%
CHEMBL2535 P11166 Glucose transporter 86.07% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.64% 99.15%
CHEMBL3194 P02766 Transthyretin 85.11% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.95% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.74% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.96% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.91% 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.
Aster bellidiastrum
Caragana halodendron
Davallia divaricata
Dolomiaea souliei
Eucalyptus camaldulensis
Garcinia mangostana
Ligularia vellerea
Lonicera hypoleuca
Nicotiana sylvestris
Polygala cyparissias
Polygala sibirica
Polygala tenuifolia
Serpocaulon triseriale

Cross-Links

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PubChem 12133315
NPASS NPC206238
LOTUS LTS0207686
wikiData Q82311455