Erypoegin F

Details

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Internal ID 30a72e88-f3f5-466f-b19f-e9b8f398dfb6
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 2-(2,4-dihydroxyphenyl)-6-methoxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H20O5/c1-12(2)4-6-16-19(25-3)9-8-14-17(11-22)21(26-20(14)16)15-7-5-13(23)10-18(15)24/h4-5,7-11,23-24H,6H2,1-3H3
InChI Key GBYUYYCUGKCGMM-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O5
Molecular Weight 352.40 g/mol
Exact Mass 352.13107373 g/mol
Topological Polar Surface Area (TPSA) 79.90 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.84
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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2-(2,4-dihydroxyphenyl)-6-methoxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-carbaldehyde
RefChem:137709
586961-23-1
CHEMBL1096946
2-(2,4-dihydroxyphenyl)-6-methoxy-7-(3-methylbut-2-en-1-yl)-1-benzofuran-3-carbaldehyde
2-(2,4-Dihydroxy-phenyl)-6-methoxy-7-(3-methyl-but-2-enyl)-benzofuran-3-carbaldehyde
3-benzofurancarboxaldehyde, 2-(2,4-dihydroxyphenyl)-6-methoxy-7-(3-methyl-2-butenyl)-
3-Formyl-2-(2',4'-dihydroxyphenyl)-6-methoxy-7-(3-methyl-2-butenyl)benzofuran
InChI=1/C21H20O5/c1-12(2)4-6-16-19(25-3)9-8-14-17(11-22)21(26-20(14)16)15-7-5-13(23)10-18(15)24/h4-5,7-11,23-24H,6H2,1-3H

2D Structure

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2D Structure of Erypoegin F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.7257 72.57%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7105 71.05%
OATP2B1 inhibitior - 0.5701 57.01%
OATP1B1 inhibitior + 0.8086 80.86%
OATP1B3 inhibitior + 0.8531 85.31%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8310 83.10%
P-glycoprotein inhibitior + 0.6555 65.55%
P-glycoprotein substrate + 0.6669 66.69%
CYP3A4 substrate + 0.5956 59.56%
CYP2C9 substrate - 0.8135 81.35%
CYP2D6 substrate - 0.7437 74.37%
CYP3A4 inhibition + 0.5815 58.15%
CYP2C9 inhibition + 0.9107 91.07%
CYP2C19 inhibition + 0.9137 91.37%
CYP2D6 inhibition - 0.6721 67.21%
CYP1A2 inhibition + 0.9091 90.91%
CYP2C8 inhibition + 0.7888 78.88%
CYP inhibitory promiscuity + 0.9833 98.33%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4609 46.09%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.5918 59.18%
Skin irritation - 0.7825 78.25%
Skin corrosion - 0.9505 95.05%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5478 54.78%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation - 0.7878 78.78%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.4787 47.87%
Acute Oral Toxicity (c) III 0.5914 59.14%
Estrogen receptor binding + 0.9414 94.14%
Androgen receptor binding + 0.8652 86.52%
Thyroid receptor binding + 0.6490 64.90%
Glucocorticoid receptor binding + 0.8572 85.72%
Aromatase binding + 0.6849 68.49%
PPAR gamma + 0.9350 93.50%
Honey bee toxicity - 0.8326 83.26%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.7055 70.55%
Fish aquatic toxicity + 0.9961 99.61%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.13% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.07% 91.11%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 97.94% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.20% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.34% 98.95%
CHEMBL3194 P02766 Transthyretin 93.82% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.29% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 91.05% 94.73%
CHEMBL1255126 O15151 Protein Mdm4 90.54% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.89% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.76% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.74% 96.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.52% 89.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.20% 94.00%
CHEMBL2535 P11166 Glucose transporter 85.65% 98.75%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 84.00% 96.90%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.64% 96.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.60% 92.94%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.47% 97.28%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.40% 94.45%
CHEMBL242 Q92731 Estrogen receptor beta 82.34% 98.35%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.38% 96.09%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.24% 83.57%

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.
Erythrina abyssinica
Erythrina poeppigiana

Cross-Links

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PubChem 637289
NPASS NPC179883
LOTUS LTS0105643
wikiData Q105006160