Vieillardiixanthone B

Details

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Internal ID 80321da0-db7f-40f3-828a-e96904d1e36e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,5-dihydroxy-3,6-dimethoxy-4-(2-methylbut-3-en-2-yl)xanthen-9-one
SMILES (Canonical) CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)OC)O)OC
SMILES (Isomeric) CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)OC)O)OC
InChI InChI=1S/C20H20O6/c1-6-20(2,3)15-13(25-5)9-11(21)14-16(22)10-7-8-12(24-4)17(23)18(10)26-19(14)15/h6-9,21,23H,1H2,2-5H3
InChI Key KJJNGJCFEOTXSG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O6
Molecular Weight 356.40 g/mol
Exact Mass 356.12598835 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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1,5-dihydroxy-3,6-dimethoxy-4-(2-methylbut-3-en-2-yl)-9H-xanthen-9-one

2D Structure

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2D Structure of Vieillardiixanthone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9774 97.74%
Caco-2 + 0.5996 59.96%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6866 68.66%
OATP2B1 inhibitior - 0.7061 70.61%
OATP1B1 inhibitior + 0.9150 91.50%
OATP1B3 inhibitior + 0.9721 97.21%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6132 61.32%
P-glycoprotein inhibitior + 0.5876 58.76%
P-glycoprotein substrate - 0.6924 69.24%
CYP3A4 substrate + 0.5731 57.31%
CYP2C9 substrate - 0.6228 62.28%
CYP2D6 substrate - 0.8460 84.60%
CYP3A4 inhibition + 0.7025 70.25%
CYP2C9 inhibition - 0.7557 75.57%
CYP2C19 inhibition + 0.7338 73.38%
CYP2D6 inhibition - 0.6977 69.77%
CYP1A2 inhibition + 0.7933 79.33%
CYP2C8 inhibition + 0.5732 57.32%
CYP inhibitory promiscuity + 0.6121 61.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5566 55.66%
Eye corrosion - 0.9838 98.38%
Eye irritation + 0.8051 80.51%
Skin irritation - 0.7557 75.57%
Skin corrosion - 0.9369 93.69%
Ames mutagenesis + 0.6836 68.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6038 60.38%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8041 80.41%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7027 70.27%
Acute Oral Toxicity (c) III 0.5884 58.84%
Estrogen receptor binding + 0.8436 84.36%
Androgen receptor binding + 0.6829 68.29%
Thyroid receptor binding + 0.7818 78.18%
Glucocorticoid receptor binding + 0.7974 79.74%
Aromatase binding + 0.8029 80.29%
PPAR gamma + 0.7550 75.50%
Honey bee toxicity - 0.8578 85.78%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9820 98.20%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.49% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.29% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.07% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.72% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.71% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.88% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.51% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.10% 94.45%
CHEMBL3194 P02766 Transthyretin 88.18% 90.71%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.83% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 86.69% 94.73%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 86.53% 98.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.10% 93.99%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 85.96% 98.21%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.56% 80.78%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.28% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.08% 89.62%
CHEMBL1937 Q92769 Histone deacetylase 2 83.09% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.27% 95.89%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.81% 89.34%

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.
Cratoxylum formosum
Garcinia vieillardii

Cross-Links

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PubChem 139078687
LOTUS LTS0060425
wikiData Q105141865