Versicone F

Details

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Internal ID 87c25c27-2d13-45b5-8d59-f9e8dc00bee3
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 2-hydroxy-7,8-dimethoxy-3-methyl-1-(2-methylbut-3-en-2-yloxymethyl)xanthen-9-one
SMILES (Canonical) CC1=CC2=C(C(=C1O)COC(C)(C)C=C)C(=O)C3=C(O2)C=CC(=C3OC)OC
SMILES (Isomeric) CC1=CC2=C(C(=C1O)COC(C)(C)C=C)C(=O)C3=C(O2)C=CC(=C3OC)OC
InChI InChI=1S/C22H24O6/c1-7-22(3,4)27-11-13-17-16(10-12(2)19(13)23)28-14-8-9-15(25-5)21(26-6)18(14)20(17)24/h7-10,23H,1,11H2,2-6H3
InChI Key REPXYLYPEUTIIE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O6
Molecular Weight 384.40 g/mol
Exact Mass 384.15728848 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Versicone F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 + 0.7202 72.02%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7104 71.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8581 85.81%
OATP1B3 inhibitior + 0.9264 92.64%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7258 72.58%
P-glycoprotein inhibitior + 0.6358 63.58%
P-glycoprotein substrate - 0.7842 78.42%
CYP3A4 substrate + 0.5952 59.52%
CYP2C9 substrate - 0.8226 82.26%
CYP2D6 substrate - 0.8330 83.30%
CYP3A4 inhibition + 0.6764 67.64%
CYP2C9 inhibition + 0.5284 52.84%
CYP2C19 inhibition + 0.7485 74.85%
CYP2D6 inhibition - 0.8382 83.82%
CYP1A2 inhibition + 0.8662 86.62%
CYP2C8 inhibition + 0.7699 76.99%
CYP inhibitory promiscuity - 0.5582 55.82%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7201 72.01%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.5154 51.54%
Skin irritation - 0.7909 79.09%
Skin corrosion - 0.9433 94.33%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4627 46.27%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.7451 74.51%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.9295 92.95%
Acute Oral Toxicity (c) III 0.5228 52.28%
Estrogen receptor binding + 0.8324 83.24%
Androgen receptor binding + 0.7522 75.22%
Thyroid receptor binding + 0.7220 72.20%
Glucocorticoid receptor binding + 0.8865 88.65%
Aromatase binding + 0.6945 69.45%
PPAR gamma + 0.8662 86.62%
Honey bee toxicity - 0.8382 83.82%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6700 67.00%
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 96.80% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.98% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.54% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.27% 94.00%
CHEMBL2581 P07339 Cathepsin D 92.77% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.61% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.56% 94.45%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 90.30% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.38% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 87.52% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.26% 85.14%
CHEMBL4530 P00488 Coagulation factor XIII 83.25% 96.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.54% 93.65%
CHEMBL1255126 O15151 Protein Mdm4 82.46% 90.20%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 81.89% 90.93%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.77% 96.00%
CHEMBL3194 P02766 Transthyretin 81.18% 90.71%

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 132543867
LOTUS LTS0196469
wikiData Q104196525