3',4',5-Trihydroxy-3-methoxy-6,7-methylenedioxyflavone 4'-glucuronide

Details

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Internal ID 746d3f34-7b26-44ae-9f8a-0442eebe3432
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glucuronides
IUPAC Name 3,4,5-trihydroxy-6-[2-hydroxy-4-(9-hydroxy-7-methoxy-8-oxo-[1,3]dioxolo[4,5-g]chromen-6-yl)phenoxy]oxane-2-carboxylic acid
SMILES (Canonical) COC1=C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=CC(=C(C=C4)OC5C(C(C(C(O5)C(=O)O)O)O)O)O
SMILES (Isomeric) COC1=C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=CC(=C(C=C4)OC5C(C(C(C(O5)C(=O)O)O)O)O)O
InChI InChI=1S/C23H20O14/c1-32-20-14(26)12-10(5-11-19(13(12)25)34-6-33-11)35-18(20)7-2-3-9(8(24)4-7)36-23-17(29)15(27)16(28)21(37-23)22(30)31/h2-5,15-17,21,23-25,27-29H,6H2,1H3,(H,30,31)
InChI Key CHIQYVBCRPLTQS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H20O14
Molecular Weight 520.40 g/mol
Exact Mass 520.08530531 g/mol
Topological Polar Surface Area (TPSA) 211.00 Ų
XlogP 1.10
Atomic LogP (AlogP) -0.12
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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CHEBI:169267
3,4,5-trihydroxy-6-[2-hydroxy-4-(9-hydroxy-7-methoxy-8-oxo-[1,3]dioxolo[4,5-g]chromen-6-yl)phenoxy]oxane-2-carboxylic acid

2D Structure

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2D Structure of 3',4',5-Trihydroxy-3-methoxy-6,7-methylenedioxyflavone 4'-glucuronide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7020 70.20%
Caco-2 - 0.8963 89.63%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7109 71.09%
OATP2B1 inhibitior - 0.5554 55.54%
OATP1B1 inhibitior + 0.9467 94.67%
OATP1B3 inhibitior + 0.9716 97.16%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5116 51.16%
P-glycoprotein inhibitior - 0.4495 44.95%
P-glycoprotein substrate - 0.7120 71.20%
CYP3A4 substrate + 0.6300 63.00%
CYP2C9 substrate - 0.8245 82.45%
CYP2D6 substrate - 0.8736 87.36%
CYP3A4 inhibition + 0.6858 68.58%
CYP2C9 inhibition + 0.6205 62.05%
CYP2C19 inhibition + 0.5172 51.72%
CYP2D6 inhibition - 0.7460 74.60%
CYP1A2 inhibition - 0.7399 73.99%
CYP2C8 inhibition + 0.8294 82.94%
CYP inhibitory promiscuity + 0.6490 64.90%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5299 52.99%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.8884 88.84%
Skin irritation - 0.7653 76.53%
Skin corrosion - 0.9319 93.19%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.8274 82.74%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8730 87.30%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.9396 93.96%
Acute Oral Toxicity (c) III 0.6759 67.59%
Estrogen receptor binding + 0.8360 83.60%
Androgen receptor binding + 0.6555 65.55%
Thyroid receptor binding - 0.5258 52.58%
Glucocorticoid receptor binding + 0.7469 74.69%
Aromatase binding + 0.5566 55.66%
PPAR gamma + 0.7109 71.09%
Honey bee toxicity - 0.7780 77.80%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9347 93.47%

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 98.90% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.58% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.49% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.86% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.26% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.58% 96.77%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.65% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.15% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.60% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.77% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.57% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.47% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.65% 99.15%
CHEMBL3194 P02766 Transthyretin 85.67% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.60% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.40% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.36% 96.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.64% 95.78%
CHEMBL3401 O75469 Pregnane X receptor 82.95% 94.73%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 82.78% 95.53%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 82.30% 95.64%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.97% 90.71%
CHEMBL261 P00915 Carbonic anhydrase I 81.34% 96.76%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.34% 80.96%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.67% 87.67%

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.
Spinacia oleracea

Cross-Links

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PubChem 74978486
LOTUS LTS0115929
wikiData Q104958849