5-Hydroxy-7,4'-dimethoxy-6-methylflavanone

Details

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Internal ID 2cd67ad6-1b67-4343-af32-a34ce7a7c1b3
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-6-methyl-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H18O5/c1-10-14(22-3)9-16-17(18(10)20)13(19)8-15(23-16)11-4-6-12(21-2)7-5-11/h4-7,9,15,20H,8H2,1-3H3
InChI Key JLCMSYSSWRCWBJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H18O5
Molecular Weight 314.30 g/mol
Exact Mass 314.11542367 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.42
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-7,4'-dimethoxy-6-methylflavanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9777 97.77%
Caco-2 + 0.7758 77.58%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8122 81.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9246 92.46%
OATP1B3 inhibitior + 0.9895 98.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7075 70.75%
P-glycoprotein inhibitior - 0.5403 54.03%
P-glycoprotein substrate - 0.9098 90.98%
CYP3A4 substrate + 0.5684 56.84%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.7747 77.47%
CYP3A4 inhibition - 0.5903 59.03%
CYP2C9 inhibition - 0.5548 55.48%
CYP2C19 inhibition + 0.7974 79.74%
CYP2D6 inhibition - 0.7590 75.90%
CYP1A2 inhibition + 0.8659 86.59%
CYP2C8 inhibition - 0.6566 65.66%
CYP inhibitory promiscuity + 0.6416 64.16%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.5769 57.69%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.6185 61.85%
Skin irritation - 0.7630 76.30%
Skin corrosion - 0.9802 98.02%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5102 51.02%
Micronuclear + 0.7559 75.59%
Hepatotoxicity - 0.6968 69.68%
skin sensitisation - 0.9583 95.83%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7750 77.50%
Acute Oral Toxicity (c) II 0.3399 33.99%
Estrogen receptor binding + 0.8401 84.01%
Androgen receptor binding + 0.6481 64.81%
Thyroid receptor binding + 0.7341 73.41%
Glucocorticoid receptor binding + 0.8028 80.28%
Aromatase binding + 0.6131 61.31%
PPAR gamma + 0.8490 84.90%
Honey bee toxicity - 0.8974 89.74%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.8516 85.16%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.35% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.03% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.08% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.26% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.20% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.47% 96.09%
CHEMBL4208 P20618 Proteasome component C5 90.16% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.24% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.91% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.82% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.24% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.19% 89.00%
CHEMBL2581 P07339 Cathepsin D 86.42% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.79% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.55% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.40% 96.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.18% 99.17%
CHEMBL2535 P11166 Glucose transporter 82.05% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.69% 90.71%

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.
Qualea labouriauana

Cross-Links

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PubChem 129834528
LOTUS LTS0133125
wikiData Q104169648