9H-Xanthen-9-one, 1-hydroxy-3,5,6-trimethoxy-

Details

Top
Internal ID 2905a1ae-6408-4e0a-9c76-2fbbf924ef0a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-hydroxy-3,5,6-trimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1)C(=O)C3=C(C=C(C=C3O2)OC)O)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)C(=O)C3=C(C=C(C=C3O2)OC)O)OC
InChI InChI=1S/C16H14O6/c1-19-8-6-10(17)13-12(7-8)22-15-9(14(13)18)4-5-11(20-2)16(15)21-3/h4-7,17H,1-3H3
InChI Key MNLGBRDSLUAKRO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H14O6
Molecular Weight 302.28 g/mol
Exact Mass 302.07903816 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
9H-Xanthen-9-one, 1-hydroxy-3,5,6-trimethoxy-
1-hydroxy-3,5,6-trimethoxyxanthen-9-one
1-Hydroxy-3,5,6-trimethoxyxanthone
Xanthen-9-one, 1-hydroxy-3,5,6-trimethoxy-
SCHEMBL7933844
DTXSID40418827
MNLGBRDSLUAKRO-UHFFFAOYSA-N
8-Hydroxy-3,4,6-trimethoxyxanthone
XH161620
XH161859
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 9H-Xanthen-9-one, 1-hydroxy-3,5,6-trimethoxy-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9769 97.69%
Caco-2 + 0.8436 84.36%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6863 68.63%
OATP2B1 inhibitior - 0.7203 72.03%
OATP1B1 inhibitior + 0.9419 94.19%
OATP1B3 inhibitior + 0.9884 98.84%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5504 55.04%
P-glycoprotein inhibitior + 0.5922 59.22%
P-glycoprotein substrate - 0.8502 85.02%
CYP3A4 substrate + 0.5310 53.10%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.6511 65.11%
CYP2C9 inhibition - 0.9806 98.06%
CYP2C19 inhibition - 0.6277 62.77%
CYP2D6 inhibition - 0.8588 85.88%
CYP1A2 inhibition + 0.9585 95.85%
CYP2C8 inhibition + 0.6306 63.06%
CYP inhibitory promiscuity - 0.5523 55.23%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6004 60.04%
Eye corrosion - 0.9679 96.79%
Eye irritation + 0.8633 86.33%
Skin irritation - 0.6803 68.03%
Skin corrosion - 0.9860 98.60%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6229 62.29%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.9331 93.31%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7112 71.12%
Acute Oral Toxicity (c) II 0.5755 57.55%
Estrogen receptor binding + 0.8213 82.13%
Androgen receptor binding + 0.7928 79.28%
Thyroid receptor binding + 0.7407 74.07%
Glucocorticoid receptor binding + 0.7831 78.31%
Aromatase binding + 0.7801 78.01%
PPAR gamma + 0.7936 79.36%
Honey bee toxicity - 0.9105 91.05%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity + 0.8585 85.85%

Targets

Top

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 95.87% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.52% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.70% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.78% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.91% 93.99%
CHEMBL2535 P11166 Glucose transporter 91.32% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.64% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 89.21% 91.49%
CHEMBL3194 P02766 Transthyretin 88.92% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.39% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.36% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.45% 99.23%
CHEMBL2581 P07339 Cathepsin D 85.72% 98.95%
CHEMBL4208 P20618 Proteasome component C5 84.78% 90.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 84.44% 80.78%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.22% 93.65%
CHEMBL1255126 O15151 Protein Mdm4 82.03% 90.20%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.89% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 80.01% 94.73%

Plants that contains it

Top
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.
Canscora alata

Cross-Links

Top
PubChem 5378599
LOTUS LTS0011059
wikiData Q82229523