1,3,7-Trihydroxy-6-methoxy-8-prenyl xanthone

Details

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Internal ID c6c073d9-0370-4c96-a693-a6c1b1599837
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 2,6,8-trihydroxy-3-methoxy-1-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=C2C(=CC(=C1O)OC)OC3=CC(=CC(=C3C2=O)O)O)C
SMILES (Isomeric) CC(=CCC1=C2C(=CC(=C1O)OC)OC3=CC(=CC(=C3C2=O)O)O)C
InChI InChI=1S/C19H18O6/c1-9(2)4-5-11-16-14(8-15(24-3)18(11)22)25-13-7-10(20)6-12(21)17(13)19(16)23/h4,6-8,20-22H,5H2,1-3H3
InChI Key SLTXVTFAQYYRPN-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O6
Molecular Weight 342.30 g/mol
Exact Mass 342.11033829 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3,7-Trihydroxy-6-methoxy-8-prenyl xanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9814 98.14%
Caco-2 + 0.8671 86.71%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Nucleus 0.4656 46.56%
OATP2B1 inhibitior - 0.5614 56.14%
OATP1B1 inhibitior + 0.8404 84.04%
OATP1B3 inhibitior + 0.9256 92.56%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5634 56.34%
P-glycoprotein inhibitior - 0.6254 62.54%
P-glycoprotein substrate - 0.5867 58.67%
CYP3A4 substrate + 0.5556 55.56%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.7033 70.33%
CYP2C9 inhibition + 0.8037 80.37%
CYP2C19 inhibition + 0.9081 90.81%
CYP2D6 inhibition + 0.7062 70.62%
CYP1A2 inhibition + 0.8876 88.76%
CYP2C8 inhibition + 0.6435 64.35%
CYP inhibitory promiscuity + 0.8928 89.28%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7089 70.89%
Eye corrosion - 0.9863 98.63%
Eye irritation + 0.7200 72.00%
Skin irritation - 0.7476 74.76%
Skin corrosion - 0.9468 94.68%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6655 66.55%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7854 78.54%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7204 72.04%
Acute Oral Toxicity (c) III 0.6679 66.79%
Estrogen receptor binding + 0.9215 92.15%
Androgen receptor binding + 0.7668 76.68%
Thyroid receptor binding + 0.5278 52.78%
Glucocorticoid receptor binding + 0.8544 85.44%
Aromatase binding + 0.7411 74.11%
PPAR gamma + 0.8886 88.86%
Honey bee toxicity - 0.8173 81.73%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9830 98.30%

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 99.13% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.87% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.33% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.32% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 92.10% 94.73%
CHEMBL3194 P02766 Transthyretin 91.48% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.18% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.64% 94.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 88.48% 98.11%
CHEMBL1929 P47989 Xanthine dehydrogenase 88.47% 96.12%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.68% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.51% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 85.96% 94.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.32% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.14% 96.09%
CHEMBL4208 P20618 Proteasome component C5 80.66% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.00% 85.14%

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.
Hypericum perforatum

Cross-Links

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PubChem 85769123
LOTUS LTS0102226
wikiData Q105255633