Montrouxanthone

Details

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Internal ID e683d20f-d2d7-42ca-b5b5-17a90830ac8b
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 4-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,5,6-tetrahydroxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O6/c1-12(2)5-4-6-13(3)7-8-14-17(25)11-18(26)19-20(27)15-9-10-16(24)21(28)23(15)29-22(14)19/h5,7,9-11,24-26,28H,4,6,8H2,1-3H3/b13-7+
InChI Key AUVRDSMLKZAONH-NTUHNPAUSA-N
Popularity 2 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) 5.00
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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RefChem:926112
4-((2E)-3,7-dimethylocta-2,6-dienyl)-1,3,5,6-tetrahydroxyxanthen-9-one
278795-77-0

2D Structure

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2D Structure of Montrouxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9603 96.03%
Caco-2 - 0.8156 81.56%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6674 66.74%
OATP2B1 inhibitior + 0.5799 57.99%
OATP1B1 inhibitior + 0.8866 88.66%
OATP1B3 inhibitior + 0.9235 92.35%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8140 81.40%
P-glycoprotein inhibitior - 0.4813 48.13%
P-glycoprotein substrate - 0.6813 68.13%
CYP3A4 substrate + 0.5432 54.32%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8389 83.89%
CYP3A4 inhibition - 0.6355 63.55%
CYP2C9 inhibition - 0.5121 51.21%
CYP2C19 inhibition + 0.5452 54.52%
CYP2D6 inhibition - 0.7603 76.03%
CYP1A2 inhibition + 0.8177 81.77%
CYP2C8 inhibition - 0.6396 63.96%
CYP inhibitory promiscuity - 0.5451 54.51%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7662 76.62%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.5933 59.33%
Skin irritation - 0.7304 73.04%
Skin corrosion - 0.9201 92.01%
Ames mutagenesis + 0.5936 59.36%
Human Ether-a-go-go-Related Gene inhibition + 0.6865 68.65%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7117 71.17%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8375 83.75%
Acute Oral Toxicity (c) III 0.5244 52.44%
Estrogen receptor binding + 0.9184 91.84%
Androgen receptor binding + 0.7899 78.99%
Thyroid receptor binding + 0.6787 67.87%
Glucocorticoid receptor binding + 0.9083 90.83%
Aromatase binding + 0.7694 76.94%
PPAR gamma + 0.9215 92.15%
Honey bee toxicity - 0.8651 86.51%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.64% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.04% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.90% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.55% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 95.12% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 95.02% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.41% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.43% 95.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.99% 92.08%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 89.29% 85.30%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.95% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.42% 99.17%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 83.89% 98.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.31% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.85% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.39% 99.23%

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.
Montrouziera sphaeroidea

Cross-Links

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PubChem 102369759
NPASS NPC248829
LOTUS LTS0092774
wikiData Q104919159