Euchrenone a4

Details

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Internal ID 2a155fb9-3a9c-4959-84ff-6400f7d2ca81
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name 2-(2,2-dimethylchromen-6-yl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H34O5/c1-17(2)7-10-21-27(32)22(11-8-18(3)4)29-26(28(21)33)23(31)16-25(34-29)19-9-12-24-20(15-19)13-14-30(5,6)35-24/h7-9,12-15,25,32-33H,10-11,16H2,1-6H3
InChI Key RPCILRXZRGPPAQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H34O5
Molecular Weight 474.60 g/mol
Exact Mass 474.24062418 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 7.50
Atomic LogP (AlogP) 7.01
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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LMPK12140311

2D Structure

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2D Structure of Euchrenone a4

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 - 0.5844 58.44%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7888 78.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8332 83.32%
OATP1B3 inhibitior + 0.9244 92.44%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9588 95.88%
P-glycoprotein inhibitior + 0.8534 85.34%
P-glycoprotein substrate - 0.5498 54.98%
CYP3A4 substrate + 0.6553 65.53%
CYP2C9 substrate - 0.7981 79.81%
CYP2D6 substrate - 0.8063 80.63%
CYP3A4 inhibition - 0.8184 81.84%
CYP2C9 inhibition + 0.7313 73.13%
CYP2C19 inhibition + 0.7890 78.90%
CYP2D6 inhibition - 0.8619 86.19%
CYP1A2 inhibition - 0.6172 61.72%
CYP2C8 inhibition + 0.5301 53.01%
CYP inhibitory promiscuity + 0.7785 77.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6776 67.76%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.7901 79.01%
Skin irritation - 0.7451 74.51%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8903 89.03%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5574 55.74%
skin sensitisation - 0.7732 77.32%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6182 61.82%
Acute Oral Toxicity (c) III 0.3814 38.14%
Estrogen receptor binding + 0.8919 89.19%
Androgen receptor binding + 0.6864 68.64%
Thyroid receptor binding + 0.6778 67.78%
Glucocorticoid receptor binding + 0.8495 84.95%
Aromatase binding + 0.7016 70.16%
PPAR gamma + 0.7855 78.55%
Honey bee toxicity - 0.7831 78.31%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9924 99.24%

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 99.74% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.48% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.39% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.61% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 95.29% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.05% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.57% 96.09%
CHEMBL240 Q12809 HERG 91.52% 89.76%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.46% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 87.69% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.65% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.02% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.78% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.46% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.51% 90.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.65% 93.40%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.32% 95.71%
CHEMBL221 P23219 Cyclooxygenase-1 80.36% 90.17%

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.
Euchresta japonica

Cross-Links

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PubChem 14284690
LOTUS LTS0045497
wikiData Q105242612