Myricetin 3,7,3'-trimethyl ether

Details

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Internal ID 7c7edd23-8df8-4025-a2a4-0f69426a9368
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 2-(3,4-dihydroxy-5-methoxyphenyl)-5-hydroxy-3,7-dimethoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O8/c1-23-9-6-10(19)14-12(7-9)26-17(18(25-3)16(14)22)8-4-11(20)15(21)13(5-8)24-2/h4-7,19-21H,1-3H3
InChI Key LVDBEFRVSYPLRQ-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O8
Molecular Weight 360.30 g/mol
Exact Mass 360.08451746 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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3,7,3'-Trimethoxy-5,4',5'-trihydroxyflavone
3,7,3'-trimethylmyricetin
CHEMBL3339151
LMPK12112781

2D Structure

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2D Structure of Myricetin 3,7,3'-trimethyl ether

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 + 0.5670 56.70%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7784 77.84%
OATP2B1 inhibitior - 0.5634 56.34%
OATP1B1 inhibitior + 0.9043 90.43%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6122 61.22%
P-glycoprotein inhibitior + 0.6274 62.74%
P-glycoprotein substrate - 0.7917 79.17%
CYP3A4 substrate + 0.5400 54.00%
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 + 0.8348 83.48%
CYP inhibitory promiscuity + 0.5295 52.95%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6022 60.22%
Eye corrosion - 0.9832 98.32%
Eye irritation + 0.6393 63.93%
Skin irritation - 0.7279 72.79%
Skin corrosion - 0.9633 96.33%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5944 59.44%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9405 94.05%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7026 70.26%
Acute Oral Toxicity (c) II 0.4732 47.32%
Estrogen receptor binding + 0.8790 87.90%
Androgen receptor binding + 0.7824 78.24%
Thyroid receptor binding + 0.5455 54.55%
Glucocorticoid receptor binding + 0.8612 86.12%
Aromatase binding + 0.7530 75.30%
PPAR gamma + 0.8238 82.38%
Honey bee toxicity - 0.9057 90.57%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5151 51.51%
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 98.61% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.67% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.03% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.79% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.00% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.47% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.63% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.61% 86.33%
CHEMBL3194 P02766 Transthyretin 87.34% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 86.77% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.47% 94.45%
CHEMBL2581 P07339 Cathepsin D 85.15% 98.95%
CHEMBL4208 P20618 Proteasome component C5 84.59% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.38% 96.09%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.65% 94.42%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.77% 95.50%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 82.01% 98.11%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.64% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.61% 99.23%
CHEMBL2424 Q04760 Glyoxalase I 81.27% 91.67%

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.
Solanum pubescens
Vitex peduncularis

Cross-Links

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PubChem 21676154
NPASS NPC58382
ChEMBL CHEMBL3339151
LOTUS LTS0047150
wikiData Q105157795