4-Hydroxy-2,3-dimethoxyxanthone

Details

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Internal ID 5c493031-bc96-437c-9558-d166a4c8572d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 4-hydroxy-2,3-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)O)OC
SMILES (Isomeric) COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)O)OC
InChI InChI=1S/C15H12O5/c1-18-11-7-9-12(16)8-5-3-4-6-10(8)20-14(9)13(17)15(11)19-2/h3-7,17H,1-2H3
InChI Key HWDHDJJDOUMUHF-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O5
Molecular Weight 272.25 g/mol
Exact Mass 272.06847348 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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10527-38-5
4-hydroxy-2,3-dimethoxyxanthen-9-one
NSC661742
9H-Xanthen-9-one, 4-hydroxy-2,3-dimethoxy-
4-Hydroxy-2,3-dimethoxy-9H-xanthen-9-one
CHEMBL3814641
2,3-Dimethoxy-4-hydroxyxanthone
DTXSID00327502
NSC-661742
4-hydroxy-2,3-dimethoxy-xanthen-9-one

2D Structure

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2D Structure of 4-Hydroxy-2,3-dimethoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9791 97.91%
Caco-2 + 0.8049 80.49%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7024 70.24%
OATP2B1 inhibitior - 0.7242 72.42%
OATP1B1 inhibitior + 0.9061 90.61%
OATP1B3 inhibitior + 0.9932 99.32%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7660 76.60%
P-glycoprotein inhibitior + 0.6479 64.79%
P-glycoprotein substrate - 0.8637 86.37%
CYP3A4 substrate + 0.5460 54.60%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition + 0.5215 52.15%
CYP2C9 inhibition - 0.8938 89.38%
CYP2C19 inhibition + 0.6902 69.02%
CYP2D6 inhibition - 0.7703 77.03%
CYP1A2 inhibition + 0.9595 95.95%
CYP2C8 inhibition + 0.5206 52.06%
CYP inhibitory promiscuity + 0.5264 52.64%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6210 62.10%
Eye corrosion - 0.9551 95.51%
Eye irritation + 0.8230 82.30%
Skin irritation - 0.5807 58.07%
Skin corrosion - 0.9822 98.22%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5972 59.72%
Micronuclear + 0.8959 89.59%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9125 91.25%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7712 77.12%
Acute Oral Toxicity (c) III 0.4994 49.94%
Estrogen receptor binding + 0.7252 72.52%
Androgen receptor binding + 0.6567 65.67%
Thyroid receptor binding + 0.6474 64.74%
Glucocorticoid receptor binding + 0.8885 88.85%
Aromatase binding + 0.8472 84.72%
PPAR gamma + 0.7645 76.45%
Honey bee toxicity - 0.9007 90.07%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8492 84.92%

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 99.50% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.83% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.14% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.99% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.75% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.38% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.06% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.66% 98.75%
CHEMBL2581 P07339 Cathepsin D 89.52% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.39% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.30% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.76% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 82.62% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.81% 92.62%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.31% 80.78%

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.
Annona muricata
Boehmeria dura
Cirsium carolinianum
Cratoxylum cochinchinense
Dipentodon sinicus
Hypericum oblongifolium
Hypericum reflexum
Kielmeyera coriacea
Kielmeyera rupestris
Kielmeyera speciosa
Pericome caudata
Piper lanceifolium

Cross-Links

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PubChem 378690
NPASS NPC88645
LOTUS LTS0194590
wikiData Q82089354