4'-Hydroxy-5-methoxy-7-(3-methyl-2,3-epoxybutoxy)flavone

Details

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Internal ID ba3871e7-d9a7-445a-9d95-507176385cf6
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 5-O-methylated flavonoids
IUPAC Name 7-[(3,3-dimethyloxiran-2-yl)methoxy]-2-(4-hydroxyphenyl)-5-methoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H20O6/c1-21(2)19(27-21)11-25-14-8-17(24-3)20-15(23)10-16(26-18(20)9-14)12-4-6-13(22)7-5-12/h4-10,19,22H,11H2,1-3H3
InChI Key OBWXJUKMULORIR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O6
Molecular Weight 368.40 g/mol
Exact Mass 368.12598835 g/mol
Topological Polar Surface Area (TPSA) 77.50 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.73
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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LMPK12110955

2D Structure

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2D Structure of 4'-Hydroxy-5-methoxy-7-(3-methyl-2,3-epoxybutoxy)flavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9776 97.76%
Caco-2 + 0.6503 65.03%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7894 78.94%
OATP2B1 inhibitior - 0.8615 86.15%
OATP1B1 inhibitior + 0.8912 89.12%
OATP1B3 inhibitior + 0.8739 87.39%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9325 93.25%
P-glycoprotein inhibitior + 0.8667 86.67%
P-glycoprotein substrate - 0.6017 60.17%
CYP3A4 substrate + 0.6325 63.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8019 80.19%
CYP3A4 inhibition - 0.5341 53.41%
CYP2C9 inhibition - 0.7376 73.76%
CYP2C19 inhibition - 0.5825 58.25%
CYP2D6 inhibition - 0.9121 91.21%
CYP1A2 inhibition - 0.7932 79.32%
CYP2C8 inhibition + 0.8484 84.84%
CYP inhibitory promiscuity - 0.7446 74.46%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6021 60.21%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.8065 80.65%
Skin irritation - 0.7896 78.96%
Skin corrosion - 0.9630 96.30%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4571 45.71%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.7690 76.90%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7070 70.70%
Acute Oral Toxicity (c) III 0.6306 63.06%
Estrogen receptor binding + 0.9376 93.76%
Androgen receptor binding + 0.9206 92.06%
Thyroid receptor binding + 0.6769 67.69%
Glucocorticoid receptor binding + 0.8950 89.50%
Aromatase binding + 0.8307 83.07%
PPAR gamma + 0.8900 89.00%
Honey bee toxicity - 0.7978 79.78%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.8571 85.71%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.92% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.44% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.87% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.53% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.69% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.75% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.55% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.07% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.07% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.29% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.92% 98.95%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 87.43% 95.78%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.80% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.55% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.33% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 82.80% 94.73%
CHEMBL2535 P11166 Glucose transporter 80.91% 98.75%
CHEMBL3194 P02766 Transthyretin 80.76% 90.71%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.57% 97.28%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.32% 92.94%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.26% 90.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.07% 97.14%

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.
Achyrocline flaccida

Cross-Links

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PubChem 44258305
LOTUS LTS0067751
wikiData Q105189196