1,3,5,8-Tetrahydroxy-4-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 617a1667-1c80-4ab1-b301-abb885fb8fe8
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 1,3,5,8-tetrahydroxy-4-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O6/c1-8(2)3-4-9-12(21)7-13(22)15-16(23)14-10(19)5-6-11(20)18(14)24-17(9)15/h3,5-7,19-22H,4H2,1-2H3
InChI Key JJNAUAFNZBCPHK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O6
Molecular Weight 328.30 g/mol
Exact Mass 328.09468823 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.28
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3,5,8-Tetrahydroxy-4-(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 + 0.9841 98.41%
Caco-2 - 0.5702 57.02%
Blood Brain Barrier - 0.5879 58.79%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5524 55.24%
OATP2B1 inhibitior - 0.5383 53.83%
OATP1B1 inhibitior + 0.9219 92.19%
OATP1B3 inhibitior + 0.9593 95.93%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5386 53.86%
P-glycoprotein inhibitior - 0.7575 75.75%
P-glycoprotein substrate - 0.8551 85.51%
CYP3A4 substrate - 0.5697 56.97%
CYP2C9 substrate - 0.5755 57.55%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition - 0.5868 58.68%
CYP2C9 inhibition + 0.9048 90.48%
CYP2C19 inhibition + 0.8543 85.43%
CYP2D6 inhibition + 0.5000 50.00%
CYP1A2 inhibition + 0.9048 90.48%
CYP2C8 inhibition - 0.8368 83.68%
CYP inhibitory promiscuity + 0.9028 90.28%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7240 72.40%
Eye corrosion - 0.9884 98.84%
Eye irritation + 0.7619 76.19%
Skin irritation - 0.6712 67.12%
Skin corrosion - 0.9008 90.08%
Ames mutagenesis + 0.7236 72.36%
Human Ether-a-go-go-Related Gene inhibition - 0.7501 75.01%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.6220 62.20%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.5575 55.75%
Acute Oral Toxicity (c) III 0.6340 63.40%
Estrogen receptor binding + 0.8135 81.35%
Androgen receptor binding + 0.7663 76.63%
Thyroid receptor binding - 0.5222 52.22%
Glucocorticoid receptor binding + 0.9173 91.73%
Aromatase binding + 0.7437 74.37%
PPAR gamma + 0.9427 94.27%
Honey bee toxicity - 0.9054 90.54%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9902 99.02%

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 98.95% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.33% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.51% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.17% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.10% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.53% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.90% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.77% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.74% 86.33%
CHEMBL3038469 P24941 CDK2/Cyclin A 84.00% 91.38%
CHEMBL3194 P02766 Transthyretin 82.87% 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.
Morus insignis

Cross-Links

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PubChem 14886041
LOTUS LTS0136760
wikiData Q105129739