Garciniaxanthone F

Details

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Internal ID b9be1ea5-0aca-46e7-90ff-9c18e69eb37a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 7,10-dihydroxy-2-(2-methoxypropan-2-yl)-8-(2-methylbut-3-en-2-yl)furo[3,2-c]xanthen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H24O6/c1-7-23(2,3)14-11-15(25)22-17(19(14)27)18(26)13-9-8-12-10-16(24(4,5)28-6)29-20(12)21(13)30-22/h7-11,25,27H,1H2,2-6H3
InChI Key OZJCGTVVJDALBR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H24O6
Molecular Weight 408.40 g/mol
Exact Mass 408.15728848 g/mol
Topological Polar Surface Area (TPSA) 89.10 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.45
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEBI:65947
7,10-dihydroxy-2-(2-methoxypropan-2-yl)-8-(2-methylbut-3-en-2-yl)-6H-furo[3,2-c]xanthen-6-one
7,10-dihydroxy-2-(2-methoxypropan-2-yl)-8-(2-methylbut-3-en-2-yl)furo[3,2-c]xanthen-6-one
7,10-dihydroxy-2-(2-methoxypropan-2-yl)-8-(2-methylbut-3-en-2-yl)-6H-furo(3,2-c)xanthen-6-one
7,10-dihydroxy-2-(2-methoxypropan-2-yl)-8-(2-methylbut-3-en-2-yl)furo(3,2-c)xanthen-6-one
RefChem:142657
Q27134448

2D Structure

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2D Structure of Garciniaxanthone F

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 - 0.6096 60.96%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7539 75.39%
OATP2B1 inhibitior - 0.5672 56.72%
OATP1B1 inhibitior + 0.8820 88.20%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6260 62.60%
P-glycoprotein inhibitior + 0.6820 68.20%
P-glycoprotein substrate - 0.6971 69.71%
CYP3A4 substrate + 0.6038 60.38%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.8596 85.96%
CYP3A4 inhibition + 0.8006 80.06%
CYP2C9 inhibition - 0.6632 66.32%
CYP2C19 inhibition + 0.7760 77.60%
CYP2D6 inhibition - 0.5731 57.31%
CYP1A2 inhibition + 0.6082 60.82%
CYP2C8 inhibition + 0.6077 60.77%
CYP inhibitory promiscuity + 0.7587 75.87%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.5145 51.45%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.6520 65.20%
Skin irritation - 0.7575 75.75%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6118 61.18%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6908 69.08%
skin sensitisation - 0.7272 72.72%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6101 61.01%
Acute Oral Toxicity (c) III 0.4474 44.74%
Estrogen receptor binding + 0.8142 81.42%
Androgen receptor binding + 0.7420 74.20%
Thyroid receptor binding + 0.7057 70.57%
Glucocorticoid receptor binding + 0.7953 79.53%
Aromatase binding + 0.7808 78.08%
PPAR gamma + 0.7226 72.26%
Honey bee toxicity - 0.7682 76.82%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9830 98.30%

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 99.06% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.20% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.48% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.57% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.44% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 92.06% 94.73%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 91.04% 80.78%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.31% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.15% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.87% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.23% 89.34%
CHEMBL1937 Q92769 Histone deacetylase 2 87.30% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.54% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.11% 89.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.93% 85.30%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.84% 93.65%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.39% 94.42%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 82.67% 98.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.47% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.43% 99.17%
CHEMBL4530 P00488 Coagulation factor XIII 80.41% 96.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.23% 97.33%

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.
Garcinia subelliptica

Cross-Links

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PubChem 10047025
NPASS NPC93092
LOTUS LTS0268268
wikiData Q27134448