1,3,8-Trihydroxy-7-methoxyxanthone

Details

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Internal ID 27367d31-22ba-4158-930d-becdd588075e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,6,8-trihydroxy-2-methoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)O
SMILES (Isomeric) COC1=C(C2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)O
InChI InChI=1S/C14H10O6/c1-19-9-3-2-8-12(13(9)17)14(18)11-7(16)4-6(15)5-10(11)20-8/h2-5,15-17H,1H3
InChI Key CNMVOPXKKWCJHT-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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There are no found synonyms.

2D Structure

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2D Structure of 1,3,8-Trihydroxy-7-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 + 0.7748 77.48%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5512 55.12%
OATP2B1 inhibitior - 0.6932 69.32%
OATP1B1 inhibitior + 0.8932 89.32%
OATP1B3 inhibitior + 0.9758 97.58%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8777 87.77%
P-glycoprotein inhibitior - 0.7533 75.33%
P-glycoprotein substrate - 0.8415 84.15%
CYP3A4 substrate + 0.5111 51.11%
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 + 0.7456 74.56%
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 + 0.8642 86.42%
Skin irritation - 0.5358 53.58%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6084 60.84%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8858 88.58%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6819 68.19%
Acute Oral Toxicity (c) III 0.7996 79.96%
Estrogen receptor binding + 0.8696 86.96%
Androgen receptor binding + 0.8160 81.60%
Thyroid receptor binding + 0.5527 55.27%
Glucocorticoid receptor binding + 0.9425 94.25%
Aromatase binding + 0.8391 83.91%
PPAR gamma + 0.8278 82.78%
Honey bee toxicity - 0.9024 90.24%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5949 59.49%
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 94.78% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.30% 94.00%
CHEMBL3194 P02766 Transthyretin 93.92% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.19% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.14% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.09% 89.00%
CHEMBL2581 P07339 Cathepsin D 90.57% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.75% 93.99%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.07% 96.12%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.97% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.18% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 86.00% 91.49%
CHEMBL4208 P20618 Proteasome component C5 84.57% 90.00%
CHEMBL2535 P11166 Glucose transporter 84.20% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 83.88% 90.20%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.60% 94.42%
CHEMBL3401 O75469 Pregnane X receptor 83.13% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.77% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.76% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.49% 96.09%

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
Canscora alata
Iris nigricans
Kielmeyera speciosa
Swertia iberica

Cross-Links

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PubChem 14839957
LOTUS LTS0123536
wikiData Q104966008