1,4,5-Trihydroxy-3,6-bis(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 5781bc59-bae7-423f-bb7b-1872546dda87
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,4,5-trihydroxy-3,6-bis(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O5/c1-12(2)5-7-14-9-10-16-21(27)18-17(24)11-15(8-6-13(3)4)20(26)23(18)28-22(16)19(14)25/h5-6,9-11,24-26H,7-8H2,1-4H3
InChI Key JBZNBOQELGIRMT-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O5
Molecular Weight 380.40 g/mol
Exact Mass 380.16237386 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.08
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,4,5-Trihydroxy-3,6-bis(3-methylbut-2-enyl)xanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 - 0.7616 76.16%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6650 66.50%
OATP2B1 inhibitior + 0.5769 57.69%
OATP1B1 inhibitior + 0.9237 92.37%
OATP1B3 inhibitior + 0.9688 96.88%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7187 71.87%
P-glycoprotein inhibitior - 0.5138 51.38%
P-glycoprotein substrate - 0.6913 69.13%
CYP3A4 substrate - 0.5177 51.77%
CYP2C9 substrate - 0.5755 57.55%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition - 0.8630 86.30%
CYP2C9 inhibition + 0.9239 92.39%
CYP2C19 inhibition + 0.9015 90.15%
CYP2D6 inhibition + 0.5630 56.30%
CYP1A2 inhibition + 0.9045 90.45%
CYP2C8 inhibition - 0.7190 71.90%
CYP inhibitory promiscuity + 0.8575 85.75%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6901 69.01%
Eye corrosion - 0.9915 99.15%
Eye irritation + 0.5587 55.87%
Skin irritation - 0.6964 69.64%
Skin corrosion - 0.9377 93.77%
Ames mutagenesis + 0.7036 70.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6162 61.62%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.7157 71.57%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7524 75.24%
Acute Oral Toxicity (c) III 0.6067 60.67%
Estrogen receptor binding + 0.8377 83.77%
Androgen receptor binding + 0.7223 72.23%
Thyroid receptor binding + 0.5837 58.37%
Glucocorticoid receptor binding + 0.8524 85.24%
Aromatase binding + 0.6932 69.32%
PPAR gamma + 0.9402 94.02%
Honey bee toxicity - 0.8918 89.18%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9932 99.32%

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 99.60% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.82% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.26% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.76% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 93.42% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.75% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.27% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.63% 93.99%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.53% 89.34%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.13% 85.30%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.67% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.99% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 82.88% 94.75%

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 subelliptica

Cross-Links

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PubChem 9842847
LOTUS LTS0155871
wikiData Q105124666