7-(3,7-Dimethylocta-2,6-dienoxy)-1,3-dihydroxyxanthen-9-one

Details

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Internal ID c412ca16-8101-4639-8aaf-f7dfe47639e8
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 7-(3,7-dimethylocta-2,6-dienoxy)-1,3-dihydroxyxanthen-9-one
SMILES (Canonical) CC(=CCCC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)C)C
InChI InChI=1S/C23H24O5/c1-14(2)5-4-6-15(3)9-10-27-17-7-8-20-18(13-17)23(26)22-19(25)11-16(24)12-21(22)28-20/h5,7-9,11-13,24-25H,4,6,10H2,1-3H3
InChI Key WOPKDKPJTJHLPB-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) 76.00 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.43
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(3,7-Dimethylocta-2,6-dienoxy)-1,3-dihydroxyxanthen-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 + 0.9762 97.62%
Caco-2 - 0.5563 55.63%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7458 74.58%
OATP2B1 inhibitior - 0.7099 70.99%
OATP1B1 inhibitior + 0.8736 87.36%
OATP1B3 inhibitior + 0.9047 90.47%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7817 78.17%
BSEP inhibitior + 0.7851 78.51%
P-glycoprotein inhibitior + 0.6822 68.22%
P-glycoprotein substrate - 0.7445 74.45%
CYP3A4 substrate + 0.6227 62.27%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition + 0.7586 75.86%
CYP2C9 inhibition + 0.5801 58.01%
CYP2C19 inhibition + 0.7529 75.29%
CYP2D6 inhibition - 0.5337 53.37%
CYP1A2 inhibition + 0.9015 90.15%
CYP2C8 inhibition + 0.6318 63.18%
CYP inhibitory promiscuity + 0.7393 73.93%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7545 75.45%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.7250 72.50%
Skin irritation - 0.7993 79.93%
Skin corrosion - 0.9593 95.93%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7549 75.49%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7729 77.29%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6924 69.24%
Acute Oral Toxicity (c) III 0.6471 64.71%
Estrogen receptor binding + 0.9376 93.76%
Androgen receptor binding + 0.8485 84.85%
Thyroid receptor binding + 0.6306 63.06%
Glucocorticoid receptor binding + 0.8803 88.03%
Aromatase binding + 0.8313 83.13%
PPAR gamma + 0.9265 92.65%
Honey bee toxicity - 0.8111 81.11%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9968 99.68%

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 98.98% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 98.27% 92.51%
CHEMBL1951 P21397 Monoamine oxidase A 98.00% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.09% 99.17%
CHEMBL1929 P47989 Xanthine dehydrogenase 96.04% 96.12%
CHEMBL3401 O75469 Pregnane X receptor 96.02% 94.73%
CHEMBL2581 P07339 Cathepsin D 95.55% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.71% 89.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.09% 92.08%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.33% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.79% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.60% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.94% 86.33%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 88.53% 93.10%
CHEMBL4208 P20618 Proteasome component C5 87.78% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.71% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.77% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.98% 93.65%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.65% 93.99%
CHEMBL2535 P11166 Glucose transporter 83.82% 98.75%
CHEMBL1937 Q92769 Histone deacetylase 2 80.89% 94.75%
CHEMBL5678 P34947 G protein-coupled receptor kinase 5 80.80% 88.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.40% 92.94%

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 cochinchinense

Cross-Links

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PubChem 78384970
LOTUS LTS0095855
wikiData Q105309631