1,3,6-Trihydroxy-2-methoxyxanthen-9-one

Details

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Internal ID 2a6a8c45-28cb-44df-a7d2-12386413b7e1
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,6-trihydroxy-2-methoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H10O6/c1-19-14-8(16)5-10-11(13(14)18)12(17)7-3-2-6(15)4-9(7)20-10/h2-5,15-16,18H,1H3
InChI Key NNFHBBNIGYWXAS-UHFFFAOYSA-N
Popularity 2 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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There are no found synonyms.

2D Structure

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2D Structure of 1,3,6-Trihydroxy-2-methoxyxanthen-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 + 0.9378 93.78%
Caco-2 + 0.7709 77.09%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5512 55.12%
OATP2B1 inhibitior - 0.6934 69.34%
OATP1B1 inhibitior + 0.8997 89.97%
OATP1B3 inhibitior + 0.9758 97.58%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8551 85.51%
P-glycoprotein inhibitior - 0.8162 81.62%
P-glycoprotein substrate - 0.7252 72.52%
CYP3A4 substrate + 0.5153 51.53%
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 + 0.5512 55.12%
CYP inhibitory promiscuity + 0.7640 76.40%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6276 62.76%
Eye corrosion - 0.9630 96.30%
Eye irritation + 0.8910 89.10%
Skin irritation - 0.5358 53.58%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7163 71.63%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8858 88.58%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8501 85.01%
Acute Oral Toxicity (c) III 0.7996 79.96%
Estrogen receptor binding + 0.8524 85.24%
Androgen receptor binding + 0.8297 82.97%
Thyroid receptor binding + 0.6232 62.32%
Glucocorticoid receptor binding + 0.9337 93.37%
Aromatase binding + 0.7516 75.16%
PPAR gamma + 0.7504 75.04%
Honey bee toxicity - 0.8800 88.00%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
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 98.73% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.35% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.89% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.36% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.12% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.75% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.62% 93.99%
CHEMBL3194 P02766 Transthyretin 88.36% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.66% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.21% 99.15%
CHEMBL2535 P11166 Glucose transporter 84.14% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.70% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.42% 99.23%
CHEMBL242 Q92731 Estrogen receptor beta 81.79% 98.35%
CHEMBL3401 O75469 Pregnane X receptor 81.49% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.47% 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.
Calophyllum inophyllum

Cross-Links

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PubChem 15380736
LOTUS LTS0046681
wikiData Q105182107