Cudratricuxanthone

Details

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Internal ID 492298da-b02b-4bea-aeb5-bbdcbeca54af
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 6,9,10-trihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H22O6/c1-11(2)5-6-12-19(26)18-20(27)14-9-15(24)16(25)10-17(14)28-22(18)13-7-8-23(3,4)29-21(12)13/h5,7-10,24-26H,6H2,1-4H3
InChI Key ZWHLXBWONQGJLD-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H22O6
Molecular Weight 394.40 g/mol
Exact Mass 394.14163842 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.76
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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6,9,10-trihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano(2,3-c)xanthen-7-one
6,9,10-trihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one
RefChem:128752
CHEMBL2437089

2D Structure

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2D Structure of Cudratricuxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 - 0.5928 59.28%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6974 69.74%
OATP2B1 inhibitior - 0.5589 55.89%
OATP1B1 inhibitior + 0.8922 89.22%
OATP1B3 inhibitior + 0.9638 96.38%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8124 81.24%
P-glycoprotein inhibitior + 0.5983 59.83%
P-glycoprotein substrate - 0.5587 55.87%
CYP3A4 substrate + 0.6108 61.08%
CYP2C9 substrate - 0.6077 60.77%
CYP2D6 substrate - 0.8218 82.18%
CYP3A4 inhibition - 0.8895 88.95%
CYP2C9 inhibition + 0.7867 78.67%
CYP2C19 inhibition + 0.8272 82.72%
CYP2D6 inhibition - 0.8704 87.04%
CYP1A2 inhibition - 0.7151 71.51%
CYP2C8 inhibition - 0.5657 56.57%
CYP inhibitory promiscuity + 0.5568 55.68%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6817 68.17%
Eye corrosion - 0.9909 99.09%
Eye irritation + 0.5826 58.26%
Skin irritation - 0.7023 70.23%
Skin corrosion - 0.9111 91.11%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4089 40.89%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.6588 65.88%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7874 78.74%
Acute Oral Toxicity (c) III 0.6749 67.49%
Estrogen receptor binding + 0.9324 93.24%
Androgen receptor binding + 0.8025 80.25%
Thyroid receptor binding + 0.5317 53.17%
Glucocorticoid receptor binding + 0.8980 89.80%
Aromatase binding + 0.7262 72.62%
PPAR gamma + 0.8773 87.73%
Honey bee toxicity - 0.6963 69.63%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9918 99.18%

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 99.88% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.06% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.11% 89.00%
CHEMBL2581 P07339 Cathepsin D 95.31% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 94.42% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 92.21% 94.73%
CHEMBL3038469 P24941 CDK2/Cyclin A 90.00% 91.38%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.99% 85.30%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 87.52% 80.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.08% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.15% 93.99%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.00% 89.34%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.76% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 84.22% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.21% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.23% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.76% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.94% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.36% 85.14%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 80.06% 97.88%

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.
Maclura tricuspidata

Cross-Links

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PubChem 25028556
LOTUS LTS0123792
wikiData Q105384956