1,5,6-Trihydroxy-3,7-dimethoxyxanthone

Details

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Internal ID 6350a4e0-b281-4204-ad43-9a4c1f96b586
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,5,6-trihydroxy-3,7-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC3=C(C(=C(C=C3C2=O)OC)O)O)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC3=C(C(=C(C=C3C2=O)OC)O)O)O
InChI InChI=1S/C15H12O7/c1-20-6-3-8(16)11-9(4-6)22-15-7(12(11)17)5-10(21-2)13(18)14(15)19/h3-5,16,18-19H,1-2H3
InChI Key UBCXIVCXMABZNZ-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O7
Molecular Weight 304.25 g/mol
Exact Mass 304.05830272 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.08
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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65008-02-8
1,5,6-Trihydroxy-3,7-Dimethoxyxanthen-9-one
AKOS040763024
1,5,6-trihydroxy-3,7-dimethoxy-xanthen-9-one

2D Structure

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2D Structure of 1,5,6-Trihydroxy-3,7-dimethoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9336 93.36%
Caco-2 - 0.5422 54.22%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7175 71.75%
OATP2B1 inhibitior - 0.5582 55.82%
OATP1B1 inhibitior + 0.8894 88.94%
OATP1B3 inhibitior + 0.9936 99.36%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7972 79.72%
P-glycoprotein inhibitior - 0.6220 62.20%
P-glycoprotein substrate - 0.8134 81.34%
CYP3A4 substrate + 0.5205 52.05%
CYP2C9 substrate - 0.6887 68.87%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition - 0.6979 69.79%
CYP2C9 inhibition - 0.9200 92.00%
CYP2C19 inhibition - 0.6079 60.79%
CYP2D6 inhibition - 0.7756 77.56%
CYP1A2 inhibition + 0.9559 95.59%
CYP2C8 inhibition + 0.5152 51.52%
CYP inhibitory promiscuity - 0.5584 55.84%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6247 62.47%
Eye corrosion - 0.9696 96.96%
Eye irritation + 0.9144 91.44%
Skin irritation - 0.6228 62.28%
Skin corrosion - 0.9539 95.39%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8028 80.28%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8959 89.59%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7923 79.23%
Acute Oral Toxicity (c) III 0.5393 53.93%
Estrogen receptor binding + 0.8902 89.02%
Androgen receptor binding + 0.6878 68.78%
Thyroid receptor binding + 0.5761 57.61%
Glucocorticoid receptor binding + 0.9301 93.01%
Aromatase binding + 0.8189 81.89%
PPAR gamma + 0.8063 80.63%
Honey bee toxicity - 0.8694 86.94%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8793 87.93%

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 98.55% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.08% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.90% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.39% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.30% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.00% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.68% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.28% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.63% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.23% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.14% 86.33%
CHEMBL3194 P02766 Transthyretin 86.56% 90.71%
CHEMBL2535 P11166 Glucose transporter 84.90% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.13% 93.99%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.44% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.09% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 82.64% 94.73%
CHEMBL4208 P20618 Proteasome component C5 81.71% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.28% 94.42%

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.
Allanblackia floribunda
Garcinia cowa

Cross-Links

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PubChem 5479778
LOTUS LTS0097323
wikiData Q105269226