6-beta-D-Glucopyranosyl-5,7-dihydroxy-4'-methoxyflavone

Details

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Internal ID ae8d9554-3b59-49e6-a585-c934558ef2c8
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid C-glycosides
IUPAC Name 5,7-dihydroxy-2-(4-methoxyphenyl)-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
SMILES (Canonical) COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)[C@H]4C([C@H]([C@@H](C(O4)CO)O)O)O)O
InChI InChI=1S/C22H22O10/c1-30-10-4-2-9(3-5-10)13-6-11(24)16-14(31-13)7-12(25)17(19(16)27)22-21(29)20(28)18(26)15(8-23)32-22/h2-7,15,18,20-23,25-29H,8H2,1H3/t15?,18-,20+,21?,22+/m1/s1
InChI Key AQHMJUSCGYYXRM-NOYZTADKSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O10
Molecular Weight 446.40 g/mol
Exact Mass 446.12129689 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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Acacetin-6-C-glucoside
6-beta-D-Glucopyranosyl-5,7-dihydroxy-4'-methoxyflavone
SCHEMBL571407
LMPK12110432

2D Structure

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2D Structure of 6-beta-D-Glucopyranosyl-5,7-dihydroxy-4'-methoxyflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6545 65.45%
Caco-2 - 0.8812 88.12%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6233 62.33%
OATP2B1 inhibitior - 0.5392 53.92%
OATP1B1 inhibitior + 0.7986 79.86%
OATP1B3 inhibitior + 0.9830 98.30%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6122 61.22%
P-glycoprotein inhibitior - 0.6396 63.96%
P-glycoprotein substrate - 0.7992 79.92%
CYP3A4 substrate + 0.6164 61.64%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.8299 82.99%
CYP3A4 inhibition - 0.7983 79.83%
CYP2C9 inhibition - 0.8483 84.83%
CYP2C19 inhibition - 0.8386 83.86%
CYP2D6 inhibition - 0.9339 93.39%
CYP1A2 inhibition - 0.8015 80.15%
CYP2C8 inhibition + 0.6205 62.05%
CYP inhibitory promiscuity - 0.6314 63.14%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6988 69.88%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.8630 86.30%
Skin irritation - 0.8040 80.40%
Skin corrosion - 0.9556 95.56%
Ames mutagenesis + 0.5499 54.99%
Human Ether-a-go-go-Related Gene inhibition - 0.4324 43.24%
Micronuclear + 0.6359 63.59%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation - 0.9200 92.00%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8993 89.93%
Acute Oral Toxicity (c) III 0.6599 65.99%
Estrogen receptor binding + 0.7723 77.23%
Androgen receptor binding + 0.7870 78.70%
Thyroid receptor binding + 0.5354 53.54%
Glucocorticoid receptor binding + 0.6833 68.33%
Aromatase binding + 0.6329 63.29%
PPAR gamma + 0.7247 72.47%
Honey bee toxicity - 0.7930 79.30%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.4258 42.58%

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 99.71% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.60% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.37% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.31% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.82% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.58% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.78% 86.92%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.11% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.93% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.57% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 87.27% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.36% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.81% 99.17%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.34% 96.21%
CHEMBL1907 P15144 Aminopeptidase N 82.69% 93.31%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.91% 95.89%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 81.80% 89.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.72% 94.45%

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.
Asphodelus ramosus

Cross-Links

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PubChem 44257871
LOTUS LTS0233988
wikiData Q104390743