4,8-Dihydroxy-2,3-dimethoxy-1-(3-methylbut-2-enyl)-9H-xanthen-9-one

Details

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Internal ID 9db33e58-5014-4300-904f-116916732428
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 4,8-dihydroxy-2,3-dimethoxy-1-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=C2C(=C(C(=C1OC)OC)O)OC3=CC=CC(=C3C2=O)O)C
SMILES (Isomeric) CC(=CCC1=C2C(=C(C(=C1OC)OC)O)OC3=CC=CC(=C3C2=O)O)C
InChI InChI=1S/C20H20O6/c1-10(2)8-9-11-14-16(22)15-12(21)6-5-7-13(15)26-19(14)17(23)20(25-4)18(11)24-3/h5-8,21,23H,9H2,1-4H3
InChI Key GVVGGAGBHDWQCK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H20O6
Molecular Weight 356.40 g/mol
Exact Mass 356.12598835 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,8-Dihydroxy-2,3-dimethoxy-1-(3-methylbut-2-enyl)-9H-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 + 0.9863 98.63%
Caco-2 + 0.8757 87.57%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6223 62.23%
OATP2B1 inhibitior - 0.7087 70.87%
OATP1B1 inhibitior + 0.8539 85.39%
OATP1B3 inhibitior + 0.9251 92.51%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6719 67.19%
P-glycoprotein inhibitior + 0.7256 72.56%
P-glycoprotein substrate - 0.7904 79.04%
CYP3A4 substrate + 0.5511 55.11%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.8396 83.96%
CYP2C9 inhibition + 0.7859 78.59%
CYP2C19 inhibition + 0.9218 92.18%
CYP2D6 inhibition + 0.6195 61.95%
CYP1A2 inhibition + 0.8872 88.72%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.8790 87.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6599 65.99%
Eye corrosion - 0.9886 98.86%
Eye irritation + 0.6796 67.96%
Skin irritation - 0.7525 75.25%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4614 46.14%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.5526 55.26%
skin sensitisation - 0.7762 77.62%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7429 74.29%
Acute Oral Toxicity (c) III 0.7411 74.11%
Estrogen receptor binding + 0.7834 78.34%
Androgen receptor binding + 0.5575 55.75%
Thyroid receptor binding - 0.5083 50.83%
Glucocorticoid receptor binding + 0.8162 81.62%
Aromatase binding - 0.5262 52.62%
PPAR gamma + 0.8933 89.33%
Honey bee toxicity - 0.8790 87.90%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9856 98.56%

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 98.66% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.68% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.48% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.69% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 92.53% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.37% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.90% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.63% 89.34%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.39% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 86.29% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.05% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.93% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.88% 99.17%
CHEMBL3959 P16083 Quinone reductase 2 82.35% 89.49%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.34% 94.03%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.04% 96.00%
CHEMBL2535 P11166 Glucose transporter 81.86% 98.75%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.98% 98.11%
CHEMBL1951 P21397 Monoamine oxidase A 80.58% 91.49%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.52% 96.95%

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
Cratoxylum formosum

Cross-Links

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PubChem 139073736
LOTUS LTS0017077
wikiData Q105021782