5,6-Dihydroxy-7,8,4'-trimethoxyflavone

Details

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Internal ID 81df5d6a-a4e8-49dc-877d-130fc0b13cfe
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 5,6-dihydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O7/c1-22-10-6-4-9(5-7-10)12-8-11(19)13-14(20)15(21)17(23-2)18(24-3)16(13)25-12/h4-8,20-21H,1-3H3
InChI Key VPLTZBCCUJNRIE-UHFFFAOYSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O7
Molecular Weight 344.30 g/mol
Exact Mass 344.08960285 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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LMPK12111449

2D Structure

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2D Structure of 5,6-Dihydroxy-7,8,4'-trimethoxyflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9464 94.64%
Caco-2 + 0.7139 71.39%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7784 77.84%
OATP2B1 inhibitior - 0.7192 71.92%
OATP1B1 inhibitior + 0.8724 87.24%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5584 55.84%
P-glycoprotein inhibitior + 0.6925 69.25%
P-glycoprotein substrate - 0.9262 92.62%
CYP3A4 substrate + 0.5252 52.52%
CYP2C9 substrate - 0.6887 68.87%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition - 0.7900 79.00%
CYP2C9 inhibition - 0.8973 89.73%
CYP2C19 inhibition - 0.7079 70.79%
CYP2D6 inhibition - 0.9069 90.69%
CYP1A2 inhibition + 0.8325 83.25%
CYP2C8 inhibition + 0.6340 63.40%
CYP inhibitory promiscuity + 0.5295 52.95%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6022 60.22%
Eye corrosion - 0.9832 98.32%
Eye irritation + 0.6088 60.88%
Skin irritation - 0.7279 72.79%
Skin corrosion - 0.9633 96.33%
Ames mutagenesis - 0.5064 50.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.8500 85.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.9405 94.05%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8295 82.95%
Acute Oral Toxicity (c) II 0.4732 47.32%
Estrogen receptor binding + 0.8676 86.76%
Androgen receptor binding + 0.9046 90.46%
Thyroid receptor binding + 0.6483 64.83%
Glucocorticoid receptor binding + 0.8197 81.97%
Aromatase binding + 0.7365 73.65%
PPAR gamma + 0.8001 80.01%
Honey bee toxicity - 0.8829 88.29%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9122 91.22%

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 98.43% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.54% 94.00%
CHEMBL2581 P07339 Cathepsin D 95.22% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.67% 99.15%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 93.28% 83.57%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.75% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.04% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.99% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 87.01% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.68% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.91% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.84% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.45% 86.92%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.47% 93.99%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.98% 81.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.78% 95.50%
CHEMBL1907 P15144 Aminopeptidase N 82.34% 93.31%
CHEMBL4208 P20618 Proteasome component C5 81.46% 90.00%

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.
Limnophila indica
Mentha aquatica

Cross-Links

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PubChem 44258635
LOTUS LTS0259026
wikiData Q105290861