2-(2,7-Dimethylocta-1,6-dienyl)-1,3,6-trihydroxy-7-methoxyxanthen-9-one

Details

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Internal ID 9529315b-d263-45cd-8dbc-1c56ba60d687
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 2-(2,7-dimethylocta-1,6-dienyl)-1,3,6-trihydroxy-7-methoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26O6/c1-13(2)7-5-6-8-14(3)9-15-17(25)11-21-22(23(15)27)24(28)16-10-20(29-4)18(26)12-19(16)30-21/h7,9-12,25-27H,5-6,8H2,1-4H3
InChI Key PFUUALWTCREXES-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O6
Molecular Weight 410.50 g/mol
Exact Mass 410.17293854 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 6.40
Atomic LogP (AlogP) 5.61
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2,7-Dimethylocta-1,6-dienyl)-1,3,6-trihydroxy-7-methoxyxanthen-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 + 0.9639 96.39%
Caco-2 + 0.5267 52.67%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5372 53.72%
OATP2B1 inhibitior - 0.7050 70.50%
OATP1B1 inhibitior + 0.8935 89.35%
OATP1B3 inhibitior + 0.9213 92.13%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7513 75.13%
P-glycoprotein inhibitior + 0.6973 69.73%
P-glycoprotein substrate - 0.5342 53.42%
CYP3A4 substrate + 0.6140 61.40%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.6461 64.61%
CYP2C9 inhibition + 0.6703 67.03%
CYP2C19 inhibition + 0.7312 73.12%
CYP2D6 inhibition + 0.5333 53.33%
CYP1A2 inhibition + 0.8518 85.18%
CYP2C8 inhibition + 0.5918 59.18%
CYP inhibitory promiscuity + 0.8232 82.32%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7275 72.75%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.6059 60.59%
Skin irritation - 0.7474 74.74%
Skin corrosion - 0.9352 93.52%
Ames mutagenesis - 0.5254 52.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6614 66.14%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5851 58.51%
skin sensitisation - 0.7606 76.06%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8725 87.25%
Acute Oral Toxicity (c) III 0.6469 64.69%
Estrogen receptor binding + 0.9014 90.14%
Androgen receptor binding + 0.6976 69.76%
Thyroid receptor binding + 0.6522 65.22%
Glucocorticoid receptor binding + 0.9195 91.95%
Aromatase binding + 0.7278 72.78%
PPAR gamma + 0.8122 81.22%
Honey bee toxicity - 0.7862 78.62%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9841 98.41%

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 99.29% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.24% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.17% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.99% 95.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.88% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 91.92% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.91% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.63% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.42% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.86% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.29% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 84.76% 98.11%
CHEMBL1937 Q92769 Histone deacetylase 2 84.58% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.24% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.20% 96.00%
CHEMBL3194 P02766 Transthyretin 81.70% 90.71%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.57% 96.90%

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 dulcis

Cross-Links

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PubChem 162914198
LOTUS LTS0098704
wikiData Q105208169