1,3,6-Trihydroxy-5-methoxy-2-(2-methylbut-3-en-2-yl)-7-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 7b468c3b-e77c-4dc8-b491-44803caa4035
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,3,6-trihydroxy-5-methoxy-2-(2-methylbut-3-en-2-yl)-7-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26O6/c1-7-24(4,5)18-15(25)11-16-17(21(18)28)20(27)14-10-13(9-8-12(2)3)19(26)23(29-6)22(14)30-16/h7-8,10-11,25-26,28H,1,9H2,2-6H3
InChI Key VHFXSSHQKAUEQC-UHFFFAOYSA-N
Popularity 3 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 6.30
Atomic LogP (AlogP) 5.04
H-Bond Acceptor 6
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 1,3,6-Trihydroxy-5-methoxy-2-(2-methylbut-3-en-2-yl)-7-(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 + 0.9810 98.10%
Caco-2 - 0.6248 62.48%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5005 50.05%
OATP2B1 inhibitior - 0.5603 56.03%
OATP1B1 inhibitior + 0.9069 90.69%
OATP1B3 inhibitior + 0.9007 90.07%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8120 81.20%
P-glycoprotein inhibitior + 0.6485 64.85%
P-glycoprotein substrate - 0.6583 65.83%
CYP3A4 substrate + 0.6252 62.52%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.8219 82.19%
CYP3A4 inhibition - 0.6353 63.53%
CYP2C9 inhibition + 0.7041 70.41%
CYP2C19 inhibition + 0.8655 86.55%
CYP2D6 inhibition - 0.5964 59.64%
CYP1A2 inhibition + 0.7634 76.34%
CYP2C8 inhibition + 0.5249 52.49%
CYP inhibitory promiscuity + 0.8046 80.46%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7324 73.24%
Eye corrosion - 0.9860 98.60%
Eye irritation + 0.5803 58.03%
Skin irritation - 0.7443 74.43%
Skin corrosion - 0.9128 91.28%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4850 48.50%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5053 50.53%
skin sensitisation - 0.7321 73.21%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8513 85.13%
Acute Oral Toxicity (c) III 0.6829 68.29%
Estrogen receptor binding + 0.8838 88.38%
Androgen receptor binding + 0.6027 60.27%
Thyroid receptor binding + 0.6893 68.93%
Glucocorticoid receptor binding + 0.8724 87.24%
Aromatase binding + 0.7289 72.89%
PPAR gamma + 0.8322 83.22%
Honey bee toxicity - 0.7152 71.52%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9917 99.17%

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 99.43% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.79% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.76% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.51% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.86% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.21% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 92.65% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.78% 94.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 90.98% 89.34%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.27% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.34% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.29% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.08% 92.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.05% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.95% 99.23%
CHEMBL1873 P00750 Tissue-type plasminogen activator 80.63% 93.33%

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.
Maclura tricuspidata

Cross-Links

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PubChem 141497209
LOTUS LTS0168520
wikiData Q104399339