3-(3,7-Dimethylocta-2,6-dienoxy)-1,7-dihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID e98acf4a-4054-40ec-b1d8-c69653a53113
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 3-(3,7-dimethylocta-2,6-dienoxy)-1,7-dihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H32O5/c1-17(2)7-6-8-19(5)13-14-32-24-16-25-26(27(30)21(24)11-9-18(3)4)28(31)22-15-20(29)10-12-23(22)33-25/h7,9-10,12-13,15-16,29-30H,6,8,11,14H2,1-5H3
InChI Key LDJAEMRUKSAODL-UHFFFAOYSA-N
Popularity 2 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) 76.00 Ų
XlogP 8.10
Atomic LogP (AlogP) 6.94
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(3,7-Dimethylocta-2,6-dienoxy)-1,7-dihydroxy-2-(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 + 0.9906 99.06%
Caco-2 - 0.6380 63.80%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8874 88.74%
OATP2B1 inhibitior - 0.5695 56.95%
OATP1B1 inhibitior + 0.8362 83.62%
OATP1B3 inhibitior + 0.8800 88.00%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9180 91.80%
P-glycoprotein inhibitior + 0.8914 89.14%
P-glycoprotein substrate + 0.5124 51.24%
CYP3A4 substrate + 0.6148 61.48%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition + 0.5806 58.06%
CYP2C9 inhibition + 0.6318 63.18%
CYP2C19 inhibition + 0.8217 82.17%
CYP2D6 inhibition - 0.6021 60.21%
CYP1A2 inhibition + 0.9712 97.12%
CYP2C8 inhibition + 0.6746 67.46%
CYP inhibitory promiscuity + 0.6921 69.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7676 76.76%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.8407 84.07%
Skin irritation - 0.8287 82.87%
Skin corrosion - 0.9621 96.21%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7301 73.01%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7844 78.44%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.9064 90.64%
Acute Oral Toxicity (c) III 0.5350 53.50%
Estrogen receptor binding + 0.9083 90.83%
Androgen receptor binding + 0.8453 84.53%
Thyroid receptor binding + 0.6430 64.30%
Glucocorticoid receptor binding + 0.8514 85.14%
Aromatase binding + 0.7334 73.34%
PPAR gamma + 0.9018 90.18%
Honey bee toxicity - 0.7727 77.27%
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 98.51% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.53% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 96.43% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.47% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.78% 89.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 93.53% 93.10%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.42% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.78% 92.08%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.52% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.95% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 85.90% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.92% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.49% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.38% 95.89%
CHEMBL2535 P11166 Glucose transporter 80.39% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.06% 90.71%

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.
Cratoxylum formosum

Cross-Links

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PubChem 75605018
LOTUS LTS0079055
wikiData Q105150236