1,3,5,6-Tetrahydroxy-8-methylxanthone

Details

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Internal ID 3402ddd1-6c34-4a1b-9250-b91deba43b39
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 3,4,6,8-tetrahydroxy-1-methylxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H10O6/c1-5-2-8(17)12(18)14-10(5)13(19)11-7(16)3-6(15)4-9(11)20-14/h2-4,15-18H,1H3
InChI Key REMPMEBGVJJOHV-UHFFFAOYSA-N
Popularity 4 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) 107.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.08
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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CHEMBL465184
HY-N12165
CS-0892685
InChI=1/C14H10O6/c1-5-2-8(17)12(18)14-10(5)13(19)11-7(16)3-6(15)4-9(11)20-14/h2-4,15-18H,1H

2D Structure

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2D Structure of 1,3,5,6-Tetrahydroxy-8-methylxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8995 89.95%
Caco-2 - 0.7369 73.69%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5796 57.96%
OATP2B1 inhibitior - 0.6593 65.93%
OATP1B1 inhibitior + 0.8710 87.10%
OATP1B3 inhibitior + 0.9898 98.98%
MATE1 inhibitior - 0.5800 58.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8027 80.27%
P-glycoprotein inhibitior - 0.9074 90.74%
P-glycoprotein substrate - 0.9020 90.20%
CYP3A4 substrate - 0.5151 51.51%
CYP2C9 substrate - 0.6465 64.65%
CYP2D6 substrate - 0.8613 86.13%
CYP3A4 inhibition + 0.5079 50.79%
CYP2C9 inhibition - 0.9319 93.19%
CYP2C19 inhibition - 0.9504 95.04%
CYP2D6 inhibition - 0.9142 91.42%
CYP1A2 inhibition + 0.9730 97.30%
CYP2C8 inhibition + 0.4929 49.29%
CYP inhibitory promiscuity - 0.5330 53.30%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6680 66.80%
Eye corrosion - 0.9838 98.38%
Eye irritation + 0.9402 94.02%
Skin irritation + 0.5647 56.47%
Skin corrosion - 0.8570 85.70%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7905 79.05%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.7083 70.83%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7045 70.45%
Acute Oral Toxicity (c) III 0.5798 57.98%
Estrogen receptor binding + 0.8058 80.58%
Androgen receptor binding + 0.6749 67.49%
Thyroid receptor binding - 0.5883 58.83%
Glucocorticoid receptor binding + 0.9377 93.77%
Aromatase binding + 0.6137 61.37%
PPAR gamma + 0.6935 69.35%
Honey bee toxicity - 0.9481 94.81%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8909 89.09%

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 98.29% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.40% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.73% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.34% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 92.34% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.76% 93.65%
CHEMBL3194 P02766 Transthyretin 91.18% 90.71%
CHEMBL1929 P47989 Xanthine dehydrogenase 90.68% 96.12%
CHEMBL2581 P07339 Cathepsin D 89.40% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.71% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.62% 99.15%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.50% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.62% 86.33%
CHEMBL4208 P20618 Proteasome component C5 84.56% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.15% 90.71%
CHEMBL4581 P52732 Kinesin-like protein 1 81.39% 93.18%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 81.26% 95.64%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.07% 99.17%
CHEMBL3038469 P24941 CDK2/Cyclin A 80.56% 91.38%

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.
There are no matching plants.

Cross-Links

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PubChem 10401107
LOTUS LTS0027551
wikiData Q77370822