1,3,5-Trihydroxy-6-methoxyxanthone

Details

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Internal ID 78640c8f-d112-42dc-b351-7c74a4de32c5
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,5-trihydroxy-6-methoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1)C(=O)C3=C(C=C(C=C3O2)O)O)O
SMILES (Isomeric) COC1=C(C2=C(C=C1)C(=O)C3=C(C=C(C=C3O2)O)O)O
InChI InChI=1S/C14H10O6/c1-19-9-3-2-7-12(17)11-8(16)4-6(15)5-10(11)20-14(7)13(9)18/h2-5,15-16,18H,1H3
InChI Key YUPPWYNUUOSXAI-UHFFFAOYSA-N
Popularity 5 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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6-Methoxy-1,3,5-trihydroxyxanthen-9-one
1,3,5-trihydroxy-6-methoxy-xanthen-9-one

2D Structure

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2D Structure of 1,3,5-Trihydroxy-6-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 + 0.5000 50.00%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5512 55.12%
OATP2B1 inhibitior - 0.6762 67.62%
OATP1B1 inhibitior + 0.9081 90.81%
OATP1B3 inhibitior + 0.9758 97.58%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7070 70.70%
P-glycoprotein inhibitior - 0.8362 83.62%
P-glycoprotein substrate - 0.6946 69.46%
CYP3A4 substrate + 0.5416 54.16%
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 + 0.7255 72.55%
CYP inhibitory promiscuity + 0.7640 76.40%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6276 62.76%
Eye corrosion - 0.9630 96.30%
Eye irritation + 0.8896 88.96%
Skin irritation - 0.5358 53.58%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8170 81.70%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8858 88.58%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6773 67.73%
Acute Oral Toxicity (c) III 0.7996 79.96%
Estrogen receptor binding + 0.8821 88.21%
Androgen receptor binding + 0.8030 80.30%
Thyroid receptor binding + 0.5401 54.01%
Glucocorticoid receptor binding + 0.8902 89.02%
Aromatase binding + 0.8148 81.48%
PPAR gamma + 0.8716 87.16%
Honey bee toxicity - 0.9036 90.36%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5749 57.49%
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 97.78% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.64% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.47% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.35% 95.56%
CHEMBL3194 P02766 Transthyretin 93.95% 90.71%
CHEMBL1951 P21397 Monoamine oxidase A 93.70% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.46% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.23% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.85% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.90% 93.99%
CHEMBL1929 P47989 Xanthine dehydrogenase 88.21% 96.12%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.01% 93.65%
CHEMBL1255126 O15151 Protein Mdm4 87.28% 90.20%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.91% 99.23%
CHEMBL2535 P11166 Glucose transporter 86.04% 98.75%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.98% 98.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.81% 99.17%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 84.61% 98.21%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.60% 89.62%
CHEMBL3401 O75469 Pregnane X receptor 81.47% 94.73%
CHEMBL4208 P20618 Proteasome component C5 80.50% 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.
Canscora alata
Cratoxylum cochinchinense
Garcinia cowa
Haploclathra leiantha
Hypericum perforatum

Cross-Links

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PubChem 5479775
NPASS NPC13373
LOTUS LTS0211178
wikiData Q105364347