1,3-Dihydroxy-5,6-dimethoxyxanthen-9-one

Details

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Internal ID ca4e74de-7393-4c9a-b8a4-3ebf6ac817be
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3-dihydroxy-5,6-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1)C(=O)C3=C(C=C(C=C3O2)O)O)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)C(=O)C3=C(C=C(C=C3O2)O)O)OC
InChI InChI=1S/C15H12O6/c1-19-10-4-3-8-13(18)12-9(17)5-7(16)6-11(12)21-14(8)15(10)20-2/h3-6,16-17H,1-2H3
InChI Key PNEJNKFUCFUNMX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O6
Molecular Weight 288.25 g/mol
Exact Mass 288.06338810 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3-Dihydroxy-5,6-dimethoxyxanthen-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 + 0.9261 92.61%
Caco-2 + 0.7804 78.04%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5592 55.92%
OATP2B1 inhibitior - 0.5769 57.69%
OATP1B1 inhibitior + 0.9318 93.18%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6565 65.65%
P-glycoprotein inhibitior - 0.6170 61.70%
P-glycoprotein substrate - 0.7880 78.80%
CYP3A4 substrate + 0.5400 54.00%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.6908 69.08%
CYP2C9 inhibition - 0.7416 74.16%
CYP2C19 inhibition + 0.6596 65.96%
CYP2D6 inhibition - 0.5311 53.11%
CYP1A2 inhibition + 0.9466 94.66%
CYP2C8 inhibition + 0.7298 72.98%
CYP inhibitory promiscuity + 0.7479 74.79%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6775 67.75%
Eye corrosion - 0.9667 96.67%
Eye irritation + 0.8776 87.76%
Skin irritation - 0.6148 61.48%
Skin corrosion - 0.9417 94.17%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6212 62.12%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8849 88.49%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6724 67.24%
Acute Oral Toxicity (c) III 0.6228 62.28%
Estrogen receptor binding + 0.8321 83.21%
Androgen receptor binding + 0.8065 80.65%
Thyroid receptor binding + 0.6861 68.61%
Glucocorticoid receptor binding + 0.8497 84.97%
Aromatase binding + 0.7185 71.85%
PPAR gamma + 0.7876 78.76%
Honey bee toxicity - 0.8972 89.72%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.8268 82.68%

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 97.12% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.68% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.35% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.16% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.05% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.67% 93.99%
CHEMBL3194 P02766 Transthyretin 92.60% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.01% 86.33%
CHEMBL2535 P11166 Glucose transporter 90.39% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 90.11% 91.49%
CHEMBL2581 P07339 Cathepsin D 88.56% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 88.22% 90.20%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.06% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.35% 99.17%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.02% 96.12%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.40% 80.78%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.44% 93.65%
CHEMBL4208 P20618 Proteasome component C5 81.66% 90.00%

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.
Garcinia oblongifolia
Haploclathra leiantha

Cross-Links

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PubChem 14077269
LOTUS LTS0117718
wikiData Q104400298