1,2,6-Trihydroxy-5-methoxy-7-(3-methylbut-2-enyl)xanthone

Details

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Internal ID 49dc67ac-403f-4fc4-b1f0-261f18c33fdf
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,2,6-trihydroxy-5-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=CC2=C(C(=C1O)OC)OC3=C(C2=O)C(=C(C=C3)O)O)C
SMILES (Isomeric) CC(=CCC1=CC2=C(C(=C1O)OC)OC3=C(C2=O)C(=C(C=C3)O)O)C
InChI InChI=1S/C19H18O6/c1-9(2)4-5-10-8-11-16(22)14-13(7-6-12(20)17(14)23)25-18(11)19(24-3)15(10)21/h4,6-8,20-21,23H,5H2,1-3H3
InChI Key SABIIYLLDNDAHN-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O6
Molecular Weight 342.30 g/mol
Exact Mass 342.11033829 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,2,6-Trihydroxy-5-methoxy-7-(3-methylbut-2-enyl)xanthone

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 + 0.5864 58.64%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6228 62.28%
OATP2B1 inhibitior - 0.5561 55.61%
OATP1B1 inhibitior + 0.9122 91.22%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5835 58.35%
P-glycoprotein inhibitior - 0.6460 64.60%
P-glycoprotein substrate - 0.8075 80.75%
CYP3A4 substrate + 0.5202 52.02%
CYP2C9 substrate - 0.6117 61.17%
CYP2D6 substrate - 0.8228 82.28%
CYP3A4 inhibition - 0.8632 86.32%
CYP2C9 inhibition + 0.6813 68.13%
CYP2C19 inhibition + 0.8598 85.98%
CYP2D6 inhibition - 0.5355 53.55%
CYP1A2 inhibition + 0.8154 81.54%
CYP2C8 inhibition - 0.5984 59.84%
CYP inhibitory promiscuity + 0.7276 72.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7145 71.45%
Eye corrosion - 0.9871 98.71%
Eye irritation + 0.7343 73.43%
Skin irritation - 0.7574 75.74%
Skin corrosion - 0.9495 94.95%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5483 54.83%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5303 53.03%
skin sensitisation - 0.7903 79.03%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8634 86.34%
Acute Oral Toxicity (c) III 0.6676 66.76%
Estrogen receptor binding + 0.9183 91.83%
Androgen receptor binding + 0.7141 71.41%
Thyroid receptor binding - 0.5612 56.12%
Glucocorticoid receptor binding + 0.8776 87.76%
Aromatase binding + 0.6727 67.27%
PPAR gamma + 0.8683 86.83%
Honey bee toxicity - 0.8274 82.74%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9885 98.85%

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 99.79% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.66% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 98.45% 91.49%
CHEMBL2581 P07339 Cathepsin D 94.40% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.82% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.30% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.64% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 91.28% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.78% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.22% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.78% 93.99%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 88.54% 85.30%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.22% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.34% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.72% 99.15%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.60% 92.62%
CHEMBL2535 P11166 Glucose transporter 82.12% 98.75%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.68% 89.34%

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 xanthochymus

Cross-Links

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PubChem 10042990
LOTUS LTS0175036
wikiData Q105248733