8-(3,3-Dimethylbutyl)-1,3,5-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 2350480e-c2bd-4399-9a11-b1bbf0306033
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 8-(3,3-dimethylbutyl)-1,3,5-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H28O5/c1-13(2)6-8-15-17(26)12-18-20(21(15)27)22(28)19-14(10-11-24(3,4)5)7-9-16(25)23(19)29-18/h6-7,9,12,25-27H,8,10-11H2,1-5H3
InChI Key ZRPYRRXCGTXJMP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H28O5
Molecular Weight 396.50 g/mol
Exact Mass 396.19367399 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 6.90
Atomic LogP (AlogP) 5.55
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-(3,3-Dimethylbutyl)-1,3,5-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 + 0.9823 98.23%
Caco-2 - 0.5330 53.30%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5956 59.56%
OATP2B1 inhibitior + 0.5784 57.84%
OATP1B1 inhibitior + 0.9116 91.16%
OATP1B3 inhibitior + 0.9272 92.72%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7295 72.95%
P-glycoprotein inhibitior - 0.4424 44.24%
P-glycoprotein substrate - 0.6595 65.95%
CYP3A4 substrate + 0.5711 57.11%
CYP2C9 substrate - 0.5797 57.97%
CYP2D6 substrate - 0.8391 83.91%
CYP3A4 inhibition - 0.6564 65.64%
CYP2C9 inhibition + 0.6994 69.94%
CYP2C19 inhibition + 0.6480 64.80%
CYP2D6 inhibition - 0.7055 70.55%
CYP1A2 inhibition + 0.7967 79.67%
CYP2C8 inhibition + 0.5734 57.34%
CYP inhibitory promiscuity + 0.7413 74.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7203 72.03%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.4831 48.31%
Skin irritation - 0.7044 70.44%
Skin corrosion - 0.9067 90.67%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5203 52.03%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.6718 67.18%
skin sensitisation - 0.6861 68.61%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7817 78.17%
Acute Oral Toxicity (c) III 0.6427 64.27%
Estrogen receptor binding + 0.8738 87.38%
Androgen receptor binding + 0.8114 81.14%
Thyroid receptor binding + 0.5374 53.74%
Glucocorticoid receptor binding + 0.8411 84.11%
Aromatase binding + 0.6735 67.35%
PPAR gamma + 0.9444 94.44%
Honey bee toxicity - 0.7579 75.79%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9916 99.16%

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 99.68% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 97.15% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 96.66% 94.73%
CHEMBL2581 P07339 Cathepsin D 95.58% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.89% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.12% 89.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.31% 95.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.93% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.91% 95.56%
CHEMBL240 Q12809 HERG 85.43% 89.76%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.24% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.00% 96.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.61% 94.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.38% 80.78%
CHEMBL3194 P02766 Transthyretin 82.03% 90.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.74% 93.99%
CHEMBL1951 P21397 Monoamine oxidase A 81.19% 91.49%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.00% 98.11%

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 nigrolineata

Cross-Links

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PubChem 162883389
LOTUS LTS0024957
wikiData Q105382169