1-Hydroxy-2,3,5-trimethoxyxanthen-9-one

Details

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Internal ID 897534d9-8dd2-4f84-8ee4-33cd71c411bb
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-hydroxy-2,3,5-trimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC=CC2=C1OC3=CC(=C(C(=C3C2=O)O)OC)OC
SMILES (Isomeric) COC1=CC=CC2=C1OC3=CC(=C(C(=C3C2=O)O)OC)OC
InChI InChI=1S/C16H14O6/c1-19-9-6-4-5-8-13(17)12-10(22-15(8)9)7-11(20-2)16(21-3)14(12)18/h4-7,18H,1-3H3
InChI Key FFVKXGZKJBHJMS-UHFFFAOYSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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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

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22804-49-5
1-hydroxy-2,3,5-trimethoxyxanthen-9-one
1-Hydroxy-2,3,5-trimethoxyxanthene
9H-Xanthen-9-one, 1-hydroxy-2,3,5-trimethoxy-
1-Hydroxy-2,3,5-trimethoxy-9H-xanthen-9-one;Tovopyrifolin C 3,5-di-O-methyl ether
Xanthone, 1-hydroxy-2,3,5-trimethoxy-
HM-1
SCHEMBL18240045
DTXSID80945485
FFVKXGZKJBHJMS-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Hydroxy-2,3,5-trimethoxyxanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9769 97.69%
Caco-2 + 0.8069 80.69%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6863 68.63%
OATP2B1 inhibitior - 0.7220 72.20%
OATP1B1 inhibitior + 0.9383 93.83%
OATP1B3 inhibitior + 0.9884 98.84%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5782 57.82%
P-glycoprotein inhibitior + 0.7023 70.23%
P-glycoprotein substrate - 0.7362 73.62%
CYP3A4 substrate + 0.5809 58.09%
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 + 0.5644 56.44%
CYP inhibitory promiscuity - 0.5523 55.23%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6004 60.04%
Eye corrosion - 0.9679 96.79%
Eye irritation + 0.8680 86.80%
Skin irritation - 0.6803 68.03%
Skin corrosion - 0.9860 98.60%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5724 57.24%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.9331 93.31%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8676 86.76%
Acute Oral Toxicity (c) II 0.5755 57.55%
Estrogen receptor binding + 0.8451 84.51%
Androgen receptor binding + 0.6887 68.87%
Thyroid receptor binding + 0.7579 75.79%
Glucocorticoid receptor binding + 0.8707 87.07%
Aromatase binding + 0.8058 80.58%
PPAR gamma + 0.8044 80.44%
Honey bee toxicity - 0.8978 89.78%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8585 85.85%

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 98.18% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.18% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.11% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.06% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.86% 86.33%
CHEMBL2535 P11166 Glucose transporter 92.26% 98.75%
CHEMBL2581 P07339 Cathepsin D 91.53% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.27% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.87% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.60% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.15% 94.45%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 86.00% 94.03%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.29% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 84.20% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.03% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 81.36% 90.20%

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.
Frasera speciosa
Halenia corniculata
Halenia elata
Halenia elliptica
Leonurus japonicus

Cross-Links

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PubChem 5318372
NPASS NPC132414
LOTUS LTS0234233
wikiData Q82922843