Emericellin

Details

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Internal ID 2fca6909-d30f-47af-a01c-e3c7545d8f2f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 8-hydroxy-1-(hydroxymethyl)-3-methyl-2-(3-methylbut-2-enoxy)-5-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H28O5/c1-14(2)6-7-17-8-9-19(27)22-23(28)21-18(13-26)24(29-11-10-15(3)4)16(5)12-20(21)30-25(17)22/h6,8-10,12,26-27H,7,11,13H2,1-5H3
InChI Key JZHBEPYIKRDWBE-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O5
Molecular Weight 408.50 g/mol
Exact Mass 408.19367399 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.31
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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Variecoxanthone B
55812-93-6
W1D56SC6FA
8-hydroxy-1-(hydroxymethyl)-3-methyl-2-(3-methylbut-2-enoxy)-5-(3-methylbut-2-enyl)xanthen-9-one
8-hydroxy-1-(hydroxymethyl)-3-methyl-5-(3-methylbut-2-en-1-yl)-2-[(3-methylbut-2-en-1-yl)oxy]-9H-xanthen-9-one
UNII-W1D56SC6FA
CHEMBL525537
SCHEMBL31647485
CHEBI:64512
DTXSID80204403
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Emericellin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 - 0.5617 56.17%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8204 82.04%
OATP2B1 inhibitior - 0.5714 57.14%
OATP1B1 inhibitior + 0.9253 92.53%
OATP1B3 inhibitior + 0.9274 92.74%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9545 95.45%
P-glycoprotein inhibitior + 0.7576 75.76%
P-glycoprotein substrate - 0.7506 75.06%
CYP3A4 substrate + 0.5828 58.28%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8189 81.89%
CYP3A4 inhibition - 0.7502 75.02%
CYP2C9 inhibition + 0.6318 63.18%
CYP2C19 inhibition + 0.8557 85.57%
CYP2D6 inhibition - 0.7288 72.88%
CYP1A2 inhibition + 0.9087 90.87%
CYP2C8 inhibition + 0.5527 55.27%
CYP inhibitory promiscuity + 0.8013 80.13%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.7667 76.67%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.7306 73.06%
Skin irritation - 0.8166 81.66%
Skin corrosion - 0.9666 96.66%
Ames mutagenesis + 0.6246 62.46%
Human Ether-a-go-go-Related Gene inhibition - 0.3867 38.67%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7317 73.17%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6043 60.43%
Acute Oral Toxicity (c) III 0.6926 69.26%
Estrogen receptor binding + 0.8194 81.94%
Androgen receptor binding + 0.7915 79.15%
Thyroid receptor binding + 0.5221 52.21%
Glucocorticoid receptor binding + 0.8909 89.09%
Aromatase binding - 0.4825 48.25%
PPAR gamma + 0.9181 91.81%
Honey bee toxicity - 0.8628 86.28%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9919 99.19%

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 98.68% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 97.32% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.16% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.88% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.54% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 91.96% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.44% 94.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 90.64% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.64% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.86% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.07% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.05% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.59% 93.99%
CHEMBL4208 P20618 Proteasome component C5 84.81% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.62% 96.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.85% 99.23%
CHEMBL3194 P02766 Transthyretin 81.23% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.23% 96.00%

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 5491812
LOTUS LTS0039999
wikiData Q27133329