methoxy-myricetin-3-O-hexoside

Details

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Internal ID c233e886-ffc1-4541-98d9-2fe8d746eb21
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SMILES (Canonical) COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O
SMILES (Isomeric) COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O
InChI InChI=1S/C22H22O13/c1-32-20-10(26)2-7(3-11(20)27)19-21(16(29)14-9(25)4-8(24)5-12(14)33-19)35-22-18(31)17(30)15(28)13(6-23)34-22/h2-5,13,15,17-18,22-28,30-31H,6H2,1H3
InChI Key SCHVWZLYQPLPJV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O13
Molecular Weight 494.40 g/mol
Exact Mass 494.10604075 g/mol
Topological Polar Surface Area (TPSA) 216.00 Ų
XlogP 0.30
Atomic LogP (AlogP) -0.53
H-Bond Acceptor 13
H-Bond Donor 8
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methoxy-myricetin-3-O-hexoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4855 48.55%
Caco-2 - 0.8470 84.70%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6190 61.90%
OATP2B1 inhibitior + 0.5860 58.60%
OATP1B1 inhibitior + 0.8815 88.15%
OATP1B3 inhibitior + 0.9740 97.40%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7168 71.68%
P-glycoprotein inhibitior - 0.5954 59.54%
P-glycoprotein substrate - 0.6909 69.09%
CYP3A4 substrate + 0.6142 61.42%
CYP2C9 substrate - 0.8485 84.85%
CYP2D6 substrate - 0.8501 85.01%
CYP3A4 inhibition - 0.9108 91.08%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9173 91.73%
CYP2D6 inhibition - 0.9514 95.14%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition + 0.7044 70.44%
CYP inhibitory promiscuity - 0.7292 72.92%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6890 68.90%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.8431 84.31%
Skin irritation - 0.8153 81.53%
Skin corrosion - 0.9600 96.00%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6483 64.83%
Micronuclear + 0.6633 66.33%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.9373 93.73%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7526 75.26%
Acute Oral Toxicity (c) III 0.6624 66.24%
Estrogen receptor binding + 0.8158 81.58%
Androgen receptor binding + 0.5767 57.67%
Thyroid receptor binding - 0.4878 48.78%
Glucocorticoid receptor binding + 0.7199 71.99%
Aromatase binding + 0.5405 54.05%
PPAR gamma + 0.6000 60.00%
Honey bee toxicity - 0.7973 79.73%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.7079 70.79%

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 99.32% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.16% 89.00%
CHEMBL2581 P07339 Cathepsin D 95.85% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.56% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.53% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.15% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.91% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 90.81% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.47% 86.33%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 87.28% 95.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.30% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.92% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.25% 86.92%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.01% 96.00%

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.
Abies nephrolepis

Cross-Links

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PubChem 73196016
LOTUS LTS0138074
wikiData Q105250149