Euchrenone a12

Details

Top
Internal ID c9573a9e-e6d5-40aa-bf20-2ba9a14b2354
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 6-prenylated flavans > 6-prenylated flavanones
IUPAC Name 5-hydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H32O6/c1-16(2)7-8-18-26(33)25-22(32)15-24(34-28(25)19-10-12-30(5,6)36-27(18)19)20-13-17-9-11-29(3,4)35-23(17)14-21(20)31/h7,9-14,24,31,33H,8,15H2,1-6H3
InChI Key AFNMVZWHERFZJC-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H32O6
Molecular Weight 488.60 g/mol
Exact Mass 488.21988874 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.68
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
LMPK12140519

2D Structure

Top
2D Structure of Euchrenone a12

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 - 0.6943 69.43%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8425 84.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8345 83.45%
OATP1B3 inhibitior + 0.9348 93.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9837 98.37%
P-glycoprotein inhibitior + 0.8422 84.22%
P-glycoprotein substrate + 0.5862 58.62%
CYP3A4 substrate + 0.6581 65.81%
CYP2C9 substrate - 0.7981 79.81%
CYP2D6 substrate - 0.8063 80.63%
CYP3A4 inhibition - 0.8633 86.33%
CYP2C9 inhibition + 0.8654 86.54%
CYP2C19 inhibition + 0.8655 86.55%
CYP2D6 inhibition - 0.8601 86.01%
CYP1A2 inhibition - 0.6415 64.15%
CYP2C8 inhibition + 0.5246 52.46%
CYP inhibitory promiscuity + 0.7979 79.79%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9713 97.13%
Carcinogenicity (trinary) Non-required 0.6207 62.07%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.7901 79.01%
Skin irritation - 0.7396 73.96%
Skin corrosion - 0.9333 93.33%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7403 74.03%
Micronuclear - 0.5741 57.41%
Hepatotoxicity + 0.5301 53.01%
skin sensitisation - 0.7497 74.97%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6429 64.29%
Acute Oral Toxicity (c) III 0.4861 48.61%
Estrogen receptor binding + 0.8803 88.03%
Androgen receptor binding + 0.6958 69.58%
Thyroid receptor binding + 0.6335 63.35%
Glucocorticoid receptor binding + 0.8001 80.01%
Aromatase binding + 0.6820 68.20%
PPAR gamma + 0.7645 76.45%
Honey bee toxicity - 0.7670 76.70%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9895 98.95%

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 99.71% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.78% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.85% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.11% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.60% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.10% 96.09%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 88.35% 80.00%
CHEMBL1951 P21397 Monoamine oxidase A 88.17% 91.49%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.90% 90.71%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.17% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.00% 86.33%
CHEMBL2413 P32246 C-C chemokine receptor type 1 84.70% 89.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.41% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.24% 99.17%
CHEMBL4208 P20618 Proteasome component C5 84.21% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.12% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.95% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.19% 95.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.91% 95.56%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 82.02% 96.37%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.75% 85.30%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.34% 89.34%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.05% 92.62%

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

Cross-Links

Top
PubChem 42608046
LOTUS LTS0163337
wikiData Q104911354