Garciosone F

Details

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Internal ID 9056e8f4-01b7-4dcc-b00a-409261b477b3
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > Pyranoxanthones
IUPAC Name 5,10-dihydroxy-9-methoxy-2,2-dimethyl-12-(2-methylbut-3-en-2-yl)pyrano[3,2-b]xanthen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H24O6/c1-7-23(2,3)16-20-13(10-11-24(4,5)30-20)18(26)15-17(25)12-8-9-14(28-6)19(27)21(12)29-22(15)16/h7-11,26-27H,1H2,2-6H3
InChI Key JPRYBVHCPBGQRZ-UHFFFAOYSA-N
Popularity 3 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) 85.20 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.01
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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12-(1,1-dimethylallyl)-5,10-dihydroxy-9-methoxy-2,2-dimethyl-pyrano[3,2-b]xanthen-6-one

2D Structure

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2D Structure of Garciosone F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9730 97.30%
Caco-2 - 0.5273 52.73%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6989 69.89%
OATP2B1 inhibitior - 0.7104 71.04%
OATP1B1 inhibitior + 0.9002 90.02%
OATP1B3 inhibitior + 0.9636 96.36%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8801 88.01%
P-glycoprotein inhibitior + 0.7361 73.61%
P-glycoprotein substrate + 0.5450 54.50%
CYP3A4 substrate + 0.6586 65.86%
CYP2C9 substrate - 0.6166 61.66%
CYP2D6 substrate - 0.8418 84.18%
CYP3A4 inhibition + 0.6953 69.53%
CYP2C9 inhibition - 0.8156 81.56%
CYP2C19 inhibition + 0.7089 70.89%
CYP2D6 inhibition - 0.6763 67.63%
CYP1A2 inhibition + 0.6073 60.73%
CYP2C8 inhibition + 0.6466 64.66%
CYP inhibitory promiscuity + 0.5615 56.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4872 48.72%
Eye corrosion - 0.9850 98.50%
Eye irritation + 0.6088 60.88%
Skin irritation - 0.7512 75.12%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis + 0.6336 63.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6670 66.70%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.7779 77.79%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.4766 47.66%
Acute Oral Toxicity (c) III 0.6115 61.15%
Estrogen receptor binding + 0.8352 83.52%
Androgen receptor binding + 0.5940 59.40%
Thyroid receptor binding + 0.8251 82.51%
Glucocorticoid receptor binding + 0.8225 82.25%
Aromatase binding + 0.8368 83.68%
PPAR gamma + 0.7903 79.03%
Honey bee toxicity - 0.7377 73.77%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9773 97.73%

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 98.42% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.46% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 95.65% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.39% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 92.70% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.11% 93.99%
CHEMBL2581 P07339 Cathepsin D 91.94% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 91.45% 90.20%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.02% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.90% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.76% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.14% 95.89%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.62% 85.30%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.21% 89.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.18% 99.23%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 81.63% 98.00%
CHEMBL3401 O75469 Pregnane X receptor 81.01% 94.73%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.57% 100.00%

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 formosum

Cross-Links

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PubChem 134816994
LOTUS LTS0199760
wikiData Q105133112