1,7-Dihydroxy-3,4,8-trimethoxyxanthone

Details

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Internal ID b7823e8e-5f29-4848-893b-30cfa48d0b99
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 2,8-dihydroxy-1,5,6-trimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C(=C1)O)C(=O)C3=C(O2)C=CC(=C3OC)O)OC
SMILES (Isomeric) COC1=C(C2=C(C(=C1)O)C(=O)C3=C(O2)C=CC(=C3OC)O)OC
InChI InChI=1S/C16H14O7/c1-20-10-6-8(18)11-13(19)12-9(23-16(11)15(10)22-3)5-4-7(17)14(12)21-2/h4-6,17-18H,1-3H3
InChI Key YOESAHHPMBOZJU-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O7
Molecular Weight 318.28 g/mol
Exact Mass 318.07395278 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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1,7-dihydroxy-3,4,8-trimethoxyxanthone

2D Structure

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2D Structure of 1,7-Dihydroxy-3,4,8-trimethoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9617 96.17%
Caco-2 + 0.6807 68.07%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7093 70.93%
OATP2B1 inhibitior - 0.7093 70.93%
OATP1B1 inhibitior + 0.9518 95.18%
OATP1B3 inhibitior + 0.9698 96.98%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6559 65.59%
P-glycoprotein inhibitior - 0.6408 64.08%
P-glycoprotein substrate - 0.9368 93.68%
CYP3A4 substrate - 0.5320 53.20%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7782 77.82%
CYP2C9 inhibition - 0.9325 93.25%
CYP2C19 inhibition - 0.5514 55.14%
CYP2D6 inhibition - 0.7363 73.63%
CYP1A2 inhibition + 0.9561 95.61%
CYP2C8 inhibition - 0.5706 57.06%
CYP inhibitory promiscuity + 0.5753 57.53%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6097 60.97%
Eye corrosion - 0.9746 97.46%
Eye irritation + 0.8651 86.51%
Skin irritation - 0.6975 69.75%
Skin corrosion - 0.9788 97.88%
Ames mutagenesis + 0.6836 68.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5346 53.46%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9328 93.28%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.7177 71.77%
Acute Oral Toxicity (c) II 0.4834 48.34%
Estrogen receptor binding + 0.8251 82.51%
Androgen receptor binding + 0.6465 64.65%
Thyroid receptor binding + 0.5639 56.39%
Glucocorticoid receptor binding + 0.8371 83.71%
Aromatase binding + 0.8229 82.29%
PPAR gamma + 0.7319 73.19%
Honey bee toxicity - 0.8986 89.86%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8676 86.76%

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 98.65% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.04% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.04% 95.56%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 90.71% 80.78%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.41% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.06% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.40% 89.00%
CHEMBL2535 P11166 Glucose transporter 88.33% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.89% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.44% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.36% 93.99%
CHEMBL3194 P02766 Transthyretin 86.35% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.70% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.89% 98.95%
CHEMBL4208 P20618 Proteasome component C5 81.07% 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.
Bredemeyera brevifolia
Bredemeyera floribunda
Jagera pseudorhus
Linum catharticum
Myristica gigantea
Nothofagus pumilio

Cross-Links

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PubChem 76317201
NPASS NPC285144
LOTUS LTS0010555
wikiData Q105351264