Euchretin A

Details

Top
Internal ID 9a082e07-8135-476a-8e58-35d67d53c3d0
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 6-prenylated isoflavanones
IUPAC Name 5,7,20-trihydroxy-17,17-dimethyl-6,8-bis(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4,6,8,13,15,19-octaen-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H30O7/c1-14(2)7-9-16-23(32)17(10-8-15(3)4)28-22(24(16)33)25(34)21-19-13-20(31)27-18(11-12-30(5,6)37-27)26(19)35-29(21)36-28/h7-8,11-13,31-33H,9-10H2,1-6H3
InChI Key PVEAILZIDDKAJE-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H30O7
Molecular Weight 502.60 g/mol
Exact Mass 502.19915329 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 8.00
Atomic LogP (AlogP) 7.01
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

Top
CHEBI:140091
LMPK12160011
5,7,20-trihydroxy-17,17-dimethyl-6,8-bis(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4,6,8,13,15,19-octaen-3-one

2D Structure

Top
2D Structure of Euchretin A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 - 0.7802 78.02%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6927 69.27%
OATP2B1 inhibitior - 0.5635 56.35%
OATP1B1 inhibitior + 0.8594 85.94%
OATP1B3 inhibitior + 0.8511 85.11%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8912 89.12%
P-glycoprotein inhibitior + 0.7544 75.44%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6234 62.34%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.8179 81.79%
CYP2C9 inhibition + 0.6628 66.28%
CYP2C19 inhibition + 0.6571 65.71%
CYP2D6 inhibition - 0.8448 84.48%
CYP1A2 inhibition - 0.5835 58.35%
CYP2C8 inhibition + 0.5186 51.86%
CYP inhibitory promiscuity + 0.7101 71.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5500 55.00%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.7529 75.29%
Skin irritation - 0.6918 69.18%
Skin corrosion - 0.9265 92.65%
Ames mutagenesis + 0.5566 55.66%
Human Ether-a-go-go-Related Gene inhibition + 0.7870 78.70%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7047 70.47%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6828 68.28%
Acute Oral Toxicity (c) III 0.4573 45.73%
Estrogen receptor binding + 0.9249 92.49%
Androgen receptor binding + 0.7539 75.39%
Thyroid receptor binding + 0.6824 68.24%
Glucocorticoid receptor binding + 0.8206 82.06%
Aromatase binding + 0.7216 72.16%
PPAR gamma + 0.8486 84.86%
Honey bee toxicity - 0.7327 73.27%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9970 99.70%

Targets

Top

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 99.79% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.71% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 96.26% 91.49%
CHEMBL2581 P07339 Cathepsin D 95.27% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.93% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 93.15% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 92.96% 94.75%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.86% 89.34%
CHEMBL3038469 P24941 CDK2/Cyclin A 88.26% 91.38%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.12% 95.56%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.62% 92.29%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.88% 85.30%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.76% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.60% 86.33%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 84.15% 80.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.69% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.28% 99.23%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.86% 96.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.69% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.45% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.02% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.94% 99.17%

Plants that contains it

Top
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.
Euchresta formosana
Euchresta japonica
Euchresta tubulosa

Cross-Links

Top
PubChem 10368763
LOTUS LTS0006597
wikiData Q104394787