Versicone G

Details

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Internal ID 93387445-b5f9-43ba-beab-5c3e65176f77
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name [7,8-dimethoxy-3-methyl-2-(3-methylbut-2-enoxy)-9-oxoxanthen-1-yl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26O7/c1-13(2)9-10-29-23-14(3)11-19-20(16(23)12-30-15(4)25)22(26)21-17(31-19)7-8-18(27-5)24(21)28-6/h7-9,11H,10,12H2,1-6H3
InChI Key GWUIVKWJVIBACO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O7
Molecular Weight 426.50 g/mol
Exact Mass 426.16785316 g/mol
Topological Polar Surface Area (TPSA) 80.30 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.68
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Versicone G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 + 0.6565 65.65%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7513 75.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9242 92.42%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9622 96.22%
P-glycoprotein inhibitior + 0.9196 91.96%
P-glycoprotein substrate - 0.7046 70.46%
CYP3A4 substrate + 0.5945 59.45%
CYP2C9 substrate - 0.6216 62.16%
CYP2D6 substrate - 0.8820 88.20%
CYP3A4 inhibition - 0.8438 84.38%
CYP2C9 inhibition + 0.6281 62.81%
CYP2C19 inhibition + 0.9091 90.91%
CYP2D6 inhibition - 0.8121 81.21%
CYP1A2 inhibition + 0.8927 89.27%
CYP2C8 inhibition + 0.7080 70.80%
CYP inhibitory promiscuity + 0.7182 71.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7228 72.28%
Eye corrosion - 0.9841 98.41%
Eye irritation - 0.7944 79.44%
Skin irritation - 0.8339 83.39%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7238 72.38%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7024 70.24%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8118 81.18%
Acute Oral Toxicity (c) III 0.6754 67.54%
Estrogen receptor binding + 0.8889 88.89%
Androgen receptor binding + 0.7455 74.55%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.8744 87.44%
Aromatase binding + 0.6987 69.87%
PPAR gamma + 0.7681 76.81%
Honey bee toxicity - 0.8634 86.34%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9965 99.65%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.70% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.72% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.24% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.02% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.67% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.08% 94.45%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.74% 89.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.60% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 90.67% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.17% 96.00%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 88.51% 90.75%
CHEMBL2535 P11166 Glucose transporter 87.01% 98.75%
CHEMBL2581 P07339 Cathepsin D 87.00% 98.95%
CHEMBL4208 P20618 Proteasome component C5 86.99% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.83% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.03% 95.50%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.63% 95.78%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.29% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 132543868
LOTUS LTS0074732
wikiData Q104167551