4,5-Dihydroxy-2,3-dimethoxy-9h-xanthen-9-one

Details

Top
Internal ID e7abc719-cf63-4728-adfd-f38fc575a1d5
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 4,5-dihydroxy-2,3-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C(=C2C(=C1)C(=O)C3=C(O2)C(=CC=C3)O)O)OC
SMILES (Isomeric) COC1=C(C(=C2C(=C1)C(=O)C3=C(O2)C(=CC=C3)O)O)OC
InChI InChI=1S/C15H12O6/c1-19-10-6-8-11(17)7-4-3-5-9(16)13(7)21-14(8)12(18)15(10)20-2/h3-6,16,18H,1-2H3
InChI Key MYOKUQAKQLUGGR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H12O6
Molecular Weight 288.25 g/mol
Exact Mass 288.06338810 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4,5-Dihydroxy-2,3-dimethoxy-9h-xanthen-9-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9642 96.42%
Caco-2 + 0.7814 78.14%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7364 73.64%
OATP2B1 inhibitior - 0.7135 71.35%
OATP1B1 inhibitior + 0.9476 94.76%
OATP1B3 inhibitior + 0.9851 98.51%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8805 88.05%
P-glycoprotein inhibitior - 0.4905 49.05%
P-glycoprotein substrate - 0.8559 85.59%
CYP3A4 substrate + 0.5454 54.54%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition - 0.6420 64.20%
CYP2C9 inhibition - 0.7071 70.71%
CYP2C19 inhibition + 0.7531 75.31%
CYP2D6 inhibition - 0.6235 62.35%
CYP1A2 inhibition + 0.9606 96.06%
CYP2C8 inhibition + 0.5770 57.70%
CYP inhibitory promiscuity + 0.6446 64.46%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6331 63.31%
Eye corrosion - 0.9655 96.55%
Eye irritation + 0.7639 76.39%
Skin irritation - 0.6099 60.99%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6255 62.55%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.9149 91.49%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8340 83.40%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding + 0.6505 65.05%
Androgen receptor binding + 0.5350 53.50%
Thyroid receptor binding + 0.6024 60.24%
Glucocorticoid receptor binding + 0.8642 86.42%
Aromatase binding + 0.8329 83.29%
PPAR gamma + 0.7426 74.26%
Honey bee toxicity - 0.8972 89.72%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5400 54.00%
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 98.61% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.08% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.18% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.13% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.70% 89.00%
CHEMBL2581 P07339 Cathepsin D 90.36% 98.95%
CHEMBL2535 P11166 Glucose transporter 90.10% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.93% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.34% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.68% 99.23%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.77% 98.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.75% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.45% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 84.64% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.28% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.28% 85.14%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.44% 94.03%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.15% 92.62%

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.
Hypericum monogynum

Cross-Links

Top
PubChem 91075024
LOTUS LTS0021412
wikiData Q105175072