4-(3,7-Dimethylocta-2,6-dienyl)-1,3,7-trihydroxyxanthen-9-one

Details

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Internal ID 9d2ded89-f94b-41d5-8ab0-0dc878d78995
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 4-(3,7-dimethylocta-2,6-dienyl)-1,3,7-trihydroxyxanthen-9-one
SMILES (Canonical) CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=CC(=C3)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=CC(=C3)O)C)C
InChI InChI=1S/C23H24O5/c1-13(2)5-4-6-14(3)7-9-16-18(25)12-19(26)21-22(27)17-11-15(24)8-10-20(17)28-23(16)21/h5,7-8,10-12,24-26H,4,6,9H2,1-3H3
InChI Key SNAUUYAKECLQLL-UHFFFAOYSA-N
Popularity 3 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) 87.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.30
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(3,7-Dimethylocta-2,6-dienyl)-1,3,7-trihydroxyxanthen-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 + 0.9843 98.43%
Caco-2 - 0.6923 69.23%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7195 71.95%
OATP2B1 inhibitior + 0.5771 57.71%
OATP1B1 inhibitior + 0.8341 83.41%
OATP1B3 inhibitior + 0.9062 90.62%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9006 90.06%
P-glycoprotein inhibitior - 0.4306 43.06%
P-glycoprotein substrate - 0.6426 64.26%
CYP3A4 substrate + 0.5665 56.65%
CYP2C9 substrate - 0.5755 57.55%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition + 0.6350 63.50%
CYP2C9 inhibition + 0.5619 56.19%
CYP2C19 inhibition + 0.6457 64.57%
CYP2D6 inhibition - 0.7189 71.89%
CYP1A2 inhibition + 0.9086 90.86%
CYP2C8 inhibition - 0.5732 57.32%
CYP inhibitory promiscuity + 0.7204 72.04%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7756 77.56%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7444 74.44%
Skin corrosion - 0.9297 92.97%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3978 39.78%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7077 70.77%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8602 86.02%
Acute Oral Toxicity (c) III 0.5043 50.43%
Estrogen receptor binding + 0.9132 91.32%
Androgen receptor binding + 0.8250 82.50%
Thyroid receptor binding + 0.6324 63.24%
Glucocorticoid receptor binding + 0.9077 90.77%
Aromatase binding + 0.7211 72.11%
PPAR gamma + 0.9445 94.45%
Honey bee toxicity - 0.8229 82.29%
Biodegradation - 0.8250 82.50%
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 99.25% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.10% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 95.77% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.57% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 94.78% 91.49%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.88% 92.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.64% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.62% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.53% 95.56%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 90.45% 93.10%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.67% 99.17%
CHEMBL3038469 P24941 CDK2/Cyclin A 83.24% 91.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.83% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.46% 86.33%

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
Garcinia fusca

Cross-Links

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PubChem 73812991
LOTUS LTS0222678
wikiData Q105256292