1,3,6-Trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 3a29557d-f738-4401-b984-4f5463699389
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,3,6-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O5/c1-9(2)3-5-11-13(20)8-15-16(17(11)21)18(22)12-6-4-10(19)7-14(12)23-15/h3-4,6-8,19-21H,5H2,1-2H3
InChI Key BUVGSDAKOBKGFK-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O5
Molecular Weight 312.30 g/mol
Exact Mass 312.09977361 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.57
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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SCHEMBL24075569
1,3,6-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one

2D Structure

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2D Structure of 1,3,6-Trihydroxy-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 + 0.9892 98.92%
Caco-2 + 0.6194 61.94%
Blood Brain Barrier - 0.5379 53.79%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6949 69.49%
OATP2B1 inhibitior - 0.5476 54.76%
OATP1B1 inhibitior + 0.8878 88.78%
OATP1B3 inhibitior + 0.9601 96.01%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6136 61.36%
P-glycoprotein inhibitior - 0.6706 67.06%
P-glycoprotein substrate - 0.5967 59.67%
CYP3A4 substrate + 0.5218 52.18%
CYP2C9 substrate - 0.5755 57.55%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition + 0.5634 56.34%
CYP2C9 inhibition + 0.9158 91.58%
CYP2C19 inhibition + 0.9038 90.38%
CYP2D6 inhibition - 0.5907 59.07%
CYP1A2 inhibition + 0.9441 94.41%
CYP2C8 inhibition + 0.4881 48.81%
CYP inhibitory promiscuity + 0.9296 92.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7173 71.73%
Eye corrosion - 0.9890 98.90%
Eye irritation + 0.8341 83.41%
Skin irritation - 0.6876 68.76%
Skin corrosion - 0.9087 90.87%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6671 66.71%
Micronuclear + 0.5500 55.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.6264 62.64%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8499 84.99%
Acute Oral Toxicity (c) III 0.6473 64.73%
Estrogen receptor binding + 0.9062 90.62%
Androgen receptor binding + 0.8565 85.65%
Thyroid receptor binding + 0.5910 59.10%
Glucocorticoid receptor binding + 0.8940 89.40%
Aromatase binding + 0.7197 71.97%
PPAR gamma + 0.9437 94.37%
Honey bee toxicity - 0.8570 85.70%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9929 99.29%

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 99.09% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.74% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.61% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.53% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 93.91% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 93.89% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.93% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.61% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.74% 93.99%
CHEMBL3194 P02766 Transthyretin 85.62% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.96% 94.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 83.89% 83.10%
CHEMBL3038469 P24941 CDK2/Cyclin A 83.42% 91.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.21% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.29% 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.
Kielmeyera coriacea

Cross-Links

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PubChem 26250237
LOTUS LTS0222368
wikiData Q104946345