7-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,5,6-tetrahydroxyxanthen-9-one

Details

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Internal ID 79068d3e-976e-40c8-8a58-56d33f7f45e9
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 7-[(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)7-8-14-9-16-21(27)19-17(25)10-15(24)11-18(19)29-23(16)22(28)20(14)26/h5,7,9-11,24-26,28H,4,6,8H2,1-3H3/b13-7+
InChI Key GIDGYMKPWWCWDW-NTUHNPAUSA-N
Popularity 3 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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There are no found synonyms.

2D Structure

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2D Structure of 7-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,5,6-tetrahydroxyxanthen-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 + 0.9297 92.97%
Caco-2 - 0.7865 78.65%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6879 68.79%
OATP2B1 inhibitior + 0.5828 58.28%
OATP1B1 inhibitior + 0.8225 82.25%
OATP1B3 inhibitior + 0.9287 92.87%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.7471 74.71%
P-glycoprotein inhibitior - 0.4842 48.42%
P-glycoprotein substrate - 0.6685 66.85%
CYP3A4 substrate + 0.5855 58.55%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8389 83.89%
CYP3A4 inhibition - 0.6610 66.10%
CYP2C9 inhibition + 0.5541 55.41%
CYP2C19 inhibition + 0.6354 63.54%
CYP2D6 inhibition - 0.6885 68.85%
CYP1A2 inhibition + 0.8395 83.95%
CYP2C8 inhibition + 0.5324 53.24%
CYP inhibitory promiscuity - 0.5116 51.16%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7641 76.41%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.6841 68.41%
Skin irritation - 0.7138 71.38%
Skin corrosion - 0.9184 91.84%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4430 44.30%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.7431 74.31%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7863 78.63%
Acute Oral Toxicity (c) III 0.5084 50.84%
Estrogen receptor binding + 0.8882 88.82%
Androgen receptor binding + 0.7508 75.08%
Thyroid receptor binding + 0.6363 63.63%
Glucocorticoid receptor binding + 0.8734 87.34%
Aromatase binding + 0.6871 68.71%
PPAR gamma + 0.9148 91.48%
Honey bee toxicity - 0.8361 83.61%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
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 99.45% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.29% 91.49%
CHEMBL2581 P07339 Cathepsin D 97.22% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 96.69% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.53% 94.45%
CHEMBL1929 P47989 Xanthine dehydrogenase 93.42% 96.12%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.12% 89.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.03% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.25% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.12% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.79% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.67% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.80% 90.71%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.76% 89.34%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.71% 93.10%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.15% 94.00%
CHEMBL2039 P27338 Monoamine oxidase B 80.89% 92.51%

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 xanthochymus

Cross-Links

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PubChem 145964319
LOTUS LTS0236273
wikiData Q105008881