2,4-Dihydroxy-6-methoxyxanthen-9-one

Details

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Internal ID c8e83af1-a41d-41fd-9b29-b60d5d7965ed
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 2,4-dihydroxy-6-methoxyxanthen-9-one
SMILES (Canonical) COC1=CC2=C(C=C1)C(=O)C3=C(O2)C(=CC(=C3)O)O
SMILES (Isomeric) COC1=CC2=C(C=C1)C(=O)C3=C(O2)C(=CC(=C3)O)O
InChI InChI=1S/C14H10O5/c1-18-8-2-3-9-12(6-8)19-14-10(13(9)17)4-7(15)5-11(14)16/h2-6,15-16H,1H3
InChI Key DOXLZPGQXHWFGC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O5
Molecular Weight 258.23 g/mol
Exact Mass 258.05282342 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,4-Dihydroxy-6-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 + 0.9404 94.04%
Caco-2 + 0.6864 68.64%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5738 57.38%
OATP2B1 inhibitior - 0.7028 70.28%
OATP1B1 inhibitior + 0.9507 95.07%
OATP1B3 inhibitior + 0.9861 98.61%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8469 84.69%
P-glycoprotein inhibitior - 0.7238 72.38%
P-glycoprotein substrate - 0.8820 88.20%
CYP3A4 substrate + 0.5085 50.85%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition + 0.7957 79.57%
CYP2C9 inhibition - 0.5790 57.90%
CYP2C19 inhibition + 0.6217 62.17%
CYP2D6 inhibition - 0.6187 61.87%
CYP1A2 inhibition + 0.9450 94.50%
CYP2C8 inhibition - 0.5645 56.45%
CYP inhibitory promiscuity + 0.6664 66.64%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5499 54.99%
Eye corrosion - 0.9486 94.86%
Eye irritation + 0.9389 93.89%
Skin irritation - 0.5968 59.68%
Skin corrosion - 0.9577 95.77%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6229 62.29%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.6560 65.60%
skin sensitisation - 0.9129 91.29%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.5935 59.35%
Acute Oral Toxicity (c) III 0.8993 89.93%
Estrogen receptor binding + 0.7061 70.61%
Androgen receptor binding + 0.8592 85.92%
Thyroid receptor binding + 0.6073 60.73%
Glucocorticoid receptor binding + 0.9160 91.60%
Aromatase binding + 0.8685 86.85%
PPAR gamma + 0.8519 85.19%
Honey bee toxicity - 0.8586 85.86%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.3970 39.70%

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 99.22% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.80% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.26% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.79% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 91.56% 91.49%
CHEMBL2581 P07339 Cathepsin D 90.93% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.21% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.17% 94.45%
CHEMBL1907 P15144 Aminopeptidase N 88.79% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.01% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.26% 93.99%
CHEMBL2535 P11166 Glucose transporter 85.91% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.57% 99.17%
CHEMBL3194 P02766 Transthyretin 84.12% 90.71%
CHEMBL1929 P47989 Xanthine dehydrogenase 83.14% 96.12%
CHEMBL2039 P27338 Monoamine oxidase B 82.99% 92.51%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.79% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.63% 94.73%
CHEMBL4208 P20618 Proteasome component C5 81.86% 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.
Gentiana asclepiadea

Cross-Links

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PubChem 163094783
LOTUS LTS0165293
wikiData Q104986304