Caloxanthone A

Details

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Internal ID 81bf14c5-e3c9-4bab-90c1-6a114b59db16
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 5,8,9-trihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
SMILES (Canonical) CC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)C
SMILES (Isomeric) CC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)C
InChI InChI=1S/C23H22O6/c1-11(2)5-6-13-19(25)15(24)9-14-21(27)18-17(28-22(13)14)10-16-12(20(18)26)7-8-23(3,4)29-16/h5,7-10,24-26H,6H2,1-4H3
InChI Key PCBFLCFTJOTIAP-UHFFFAOYSA-N
Popularity 1 reference 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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There are no found synonyms.

2D Structure

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2D Structure of Caloxanthone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9732 97.32%
Caco-2 - 0.6583 65.83%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6936 69.36%
OATP2B1 inhibitior - 0.5590 55.90%
OATP1B1 inhibitior + 0.8702 87.02%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8518 85.18%
P-glycoprotein inhibitior + 0.6483 64.83%
P-glycoprotein substrate - 0.5534 55.34%
CYP3A4 substrate + 0.6001 60.01%
CYP2C9 substrate - 0.6077 60.77%
CYP2D6 substrate - 0.8218 82.18%
CYP3A4 inhibition - 0.9054 90.54%
CYP2C9 inhibition + 0.8115 81.15%
CYP2C19 inhibition + 0.8352 83.52%
CYP2D6 inhibition - 0.7977 79.77%
CYP1A2 inhibition - 0.6262 62.62%
CYP2C8 inhibition + 0.4576 45.76%
CYP inhibitory promiscuity + 0.6049 60.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6732 67.32%
Eye corrosion - 0.9914 99.14%
Eye irritation + 0.5232 52.32%
Skin irritation - 0.6971 69.71%
Skin corrosion - 0.9077 90.77%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5449 54.49%
skin sensitisation - 0.7050 70.50%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.8191 81.91%
Acute Oral Toxicity (c) III 0.6179 61.79%
Estrogen receptor binding + 0.9618 96.18%
Androgen receptor binding + 0.7786 77.86%
Thyroid receptor binding + 0.6698 66.98%
Glucocorticoid receptor binding + 0.9529 95.29%
Aromatase binding + 0.7640 76.40%
PPAR gamma + 0.9142 91.42%
Honey bee toxicity - 0.7897 78.97%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9924 99.24%

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 99.74% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.66% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.63% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.96% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.16% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 92.83% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.51% 85.14%
CHEMBL3038469 P24941 CDK2/Cyclin A 91.62% 91.38%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.86% 89.34%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 88.39% 85.30%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.54% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.49% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.51% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.27% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.25% 86.33%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 81.04% 80.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.64% 100.00%

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.
Aster bellidiastrum
Calophyllum inophyllum
Caragana halodendron
Davallia divaricata
Dolomiaea souliei
Eucalyptus camaldulensis
Garcinia mangostana
Ligularia vellerea
Lonicera hypoleuca
Nicotiana sylvestris
Serpocaulon triseriale

Cross-Links

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PubChem 10046140
NPASS NPC124319
LOTUS LTS0043089
wikiData Q104399019