1,3,5-Tris(3-methylbut-2-enoxy)xanthen-9-one

Details

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Internal ID c6e85c66-3482-4a88-89d0-2085ce073bda
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,5-tris(3-methylbut-2-enoxy)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H32O5/c1-18(2)10-13-30-21-16-24(32-15-12-20(5)6)26-25(17-21)33-28-22(27(26)29)8-7-9-23(28)31-14-11-19(3)4/h7-12,16-17H,13-15H2,1-6H3
InChI Key KZLPWSCXPOCXQL-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C28H32O5
Molecular Weight 448.50 g/mol
Exact Mass 448.22497412 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 7.40
Atomic LogP (AlogP) 6.98
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3,5-Tris(3-methylbut-2-enoxy)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 + 0.9933 99.33%
Caco-2 + 0.5490 54.90%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6883 68.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9527 95.27%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9949 99.49%
P-glycoprotein inhibitior + 0.9602 96.02%
P-glycoprotein substrate - 0.7795 77.95%
CYP3A4 substrate + 0.5865 58.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7963 79.63%
CYP3A4 inhibition - 0.6926 69.26%
CYP2C9 inhibition + 0.5472 54.72%
CYP2C19 inhibition + 0.8643 86.43%
CYP2D6 inhibition - 0.7076 70.76%
CYP1A2 inhibition + 0.9149 91.49%
CYP2C8 inhibition - 0.6426 64.26%
CYP inhibitory promiscuity + 0.8642 86.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6511 65.11%
Eye corrosion - 0.9778 97.78%
Eye irritation - 0.7382 73.82%
Skin irritation - 0.7691 76.91%
Skin corrosion - 0.9734 97.34%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9106 91.06%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.5033 50.33%
skin sensitisation - 0.6231 62.31%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6321 63.21%
Acute Oral Toxicity (c) III 0.7296 72.96%
Estrogen receptor binding + 0.8915 89.15%
Androgen receptor binding + 0.8289 82.89%
Thyroid receptor binding + 0.6430 64.30%
Glucocorticoid receptor binding + 0.8322 83.22%
Aromatase binding + 0.5696 56.96%
PPAR gamma + 0.8440 84.40%
Honey bee toxicity - 0.8528 85.28%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9826 98.26%

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 97.23% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.50% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.35% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.79% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.16% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.65% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.58% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.10% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.88% 99.17%
CHEMBL2535 P11166 Glucose transporter 87.77% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.06% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.47% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.61% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.67% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.93% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 24814164
LOTUS LTS0246743
wikiData Q105148323