1,5-Dihydroxy-3,6-dimethoxy-2,7-diprenylxanthone

Details

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Internal ID 2ba924d5-862f-4105-a9dd-5446a30eeee2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,5-dihydroxy-3,6-dimethoxy-2,7-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H28O6/c1-13(2)7-9-15-11-17-22(27)20-19(31-25(17)23(28)24(15)30-6)12-18(29-5)16(21(20)26)10-8-14(3)4/h7-8,11-12,26,28H,9-10H2,1-6H3
InChI Key IRSFNWZFZSTWDA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O6
Molecular Weight 424.50 g/mol
Exact Mass 424.18858861 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.39
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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1,5-dihydroxy-3,6-dimethoxy-2,7-diprenylxanthone
1180526-86-6

2D Structure

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2D Structure of 1,5-Dihydroxy-3,6-dimethoxy-2,7-diprenylxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9785 97.85%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5950 59.50%
OATP2B1 inhibitior - 0.5719 57.19%
OATP1B1 inhibitior + 0.8919 89.19%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9028 90.28%
P-glycoprotein inhibitior + 0.8032 80.32%
P-glycoprotein substrate - 0.5839 58.39%
CYP3A4 substrate + 0.5667 56.67%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.8605 86.05%
CYP2C9 inhibition + 0.8972 89.72%
CYP2C19 inhibition + 0.9226 92.26%
CYP2D6 inhibition + 0.8037 80.37%
CYP1A2 inhibition + 0.9107 91.07%
CYP2C8 inhibition + 0.5276 52.76%
CYP inhibitory promiscuity + 0.8649 86.49%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6900 69.00%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.6843 68.43%
Skin irritation - 0.7562 75.62%
Skin corrosion - 0.9540 95.40%
Ames mutagenesis + 0.5336 53.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5432 54.32%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8057 80.57%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.8463 84.63%
Acute Oral Toxicity (c) III 0.6502 65.02%
Estrogen receptor binding + 0.8961 89.61%
Androgen receptor binding + 0.5890 58.90%
Thyroid receptor binding + 0.5765 57.65%
Glucocorticoid receptor binding + 0.8112 81.12%
Aromatase binding + 0.7518 75.18%
PPAR gamma + 0.8501 85.01%
Honey bee toxicity - 0.7555 75.55%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9881 98.81%

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 99.35% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.53% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.79% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.75% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 92.24% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.87% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.54% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.29% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.09% 94.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 90.94% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.98% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.09% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.21% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.52% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.70% 99.23%
CHEMBL2535 P11166 Glucose transporter 81.55% 98.75%

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.
Garcinia griffithii

Cross-Links

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PubChem 44191407
LOTUS LTS0151014
wikiData Q105119086