Cudratricusxanthone E

Details

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Internal ID 59361167-5479-4936-9f34-a7c725ebfb4d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 1,3,6,7-tetrahydroxy-2,4-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O6/c1-11(2)5-7-13-20(26)14(8-6-12(3)4)23-19(21(13)27)22(28)15-9-16(24)17(25)10-18(15)29-23/h5-6,9-10,24-27H,7-8H2,1-4H3
InChI Key WOYJYLIGVMHOMK-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O6
Molecular Weight 396.40 g/mol
Exact Mass 396.15728848 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 4.79
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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CHEMBL1173562

2D Structure

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2D Structure of Cudratricusxanthone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9735 97.35%
Caco-2 - 0.6505 65.05%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5918 59.18%
OATP2B1 inhibitior + 0.5858 58.58%
OATP1B1 inhibitior + 0.8970 89.70%
OATP1B3 inhibitior + 0.9677 96.77%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5945 59.45%
P-glycoprotein inhibitior - 0.5165 51.65%
P-glycoprotein substrate - 0.7865 78.65%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8389 83.89%
CYP3A4 inhibition - 0.8334 83.34%
CYP2C9 inhibition + 0.6722 67.22%
CYP2C19 inhibition + 0.6740 67.40%
CYP2D6 inhibition - 0.7142 71.42%
CYP1A2 inhibition + 0.7721 77.21%
CYP2C8 inhibition - 0.8226 82.26%
CYP inhibitory promiscuity + 0.6955 69.55%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7454 74.54%
Eye corrosion - 0.9893 98.93%
Eye irritation + 0.6494 64.94%
Skin irritation - 0.7188 71.88%
Skin corrosion - 0.9236 92.36%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6052 60.52%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.6197 61.97%
skin sensitisation - 0.6851 68.51%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7933 79.33%
Acute Oral Toxicity (c) III 0.5956 59.56%
Estrogen receptor binding + 0.9030 90.30%
Androgen receptor binding + 0.7881 78.81%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.8554 85.54%
Aromatase binding + 0.6852 68.52%
PPAR gamma + 0.9301 93.01%
Honey bee toxicity - 0.8092 80.92%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9954 99.54%

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 99.49% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.61% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.99% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 93.57% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.19% 89.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.93% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.66% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 88.24% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.57% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.44% 99.23%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.56% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.29% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.12% 98.11%

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 lancilimba
Maclura tricuspidata

Cross-Links

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PubChem 49799569
LOTUS LTS0090626
wikiData Q105309746