Trapezifolixanthone

Details

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Internal ID f6675c06-9e79-47d6-8cc2-9fdeb0aabab1
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 5,10-dihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
SMILES (Canonical) CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)C=CC(O2)(C)C)C
SMILES (Isomeric) CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)C=CC(O2)(C)C)C
InChI InChI=1S/C23H22O5/c1-12(2)8-9-15-20-14(10-11-23(3,4)28-20)19(26)17-18(25)13-6-5-7-16(24)21(13)27-22(15)17/h5-8,10-11,24,26H,9H2,1-4H3
InChI Key YWHROXVOOAEFOY-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C23H22O5
Molecular Weight 378.40 g/mol
Exact Mass 378.14672380 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.05
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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50816-23-4
Toxyloxanthone A
Trapezifoli-xanthone
2H,6H-Pyrano[3,2-b]xanthen-6-one, 5,10-dihydroxy-2,2-dimethyl-12-(3-methyl-2-butenyl)-
5,10-dihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
SCHEMBL17057006
DTXSID90198844

2D Structure

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2D Structure of Trapezifolixanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.5920 59.20%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7159 71.59%
OATP2B1 inhibitior - 0.5690 56.90%
OATP1B1 inhibitior + 0.8835 88.35%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8552 85.52%
P-glycoprotein inhibitior + 0.6814 68.14%
P-glycoprotein substrate - 0.5105 51.05%
CYP3A4 substrate + 0.6425 64.25%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.8677 86.77%
CYP2C9 inhibition + 0.7303 73.03%
CYP2C19 inhibition + 0.7855 78.55%
CYP2D6 inhibition - 0.7304 73.04%
CYP1A2 inhibition - 0.5591 55.91%
CYP2C8 inhibition + 0.4518 45.18%
CYP inhibitory promiscuity + 0.7538 75.38%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6419 64.19%
Eye corrosion - 0.9903 99.03%
Eye irritation + 0.6703 67.03%
Skin irritation - 0.6959 69.59%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4221 42.21%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.5449 54.49%
skin sensitisation - 0.6213 62.13%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7522 75.22%
Acute Oral Toxicity (c) III 0.7431 74.31%
Estrogen receptor binding + 0.8971 89.71%
Androgen receptor binding + 0.6816 68.16%
Thyroid receptor binding + 0.6952 69.52%
Glucocorticoid receptor binding + 0.9011 90.11%
Aromatase binding + 0.7168 71.68%
PPAR gamma + 0.9047 90.47%
Honey bee toxicity - 0.7759 77.59%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9822 98.22%

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 99.54% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.93% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 96.96% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.66% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 95.36% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 95.27% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.91% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.80% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.78% 85.30%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.46% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.94% 99.23%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 88.10% 83.10%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.23% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.66% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.82% 86.33%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.01% 90.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.90% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 81.21% 90.17%

Cross-Links

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PubChem 188341
NPASS NPC279242
LOTUS LTS0161438
wikiData Q83071693