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

Details

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Internal ID 45d14662-1f4c-41f9-802d-3df9dc7df507
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glucuronides > Flavonoid-3-O-glucuronides
IUPAC Name 3,4,5-trihydroxy-6-[[9-hydroxy-6-(3-hydroxy-4-methoxyphenyl)-8-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl]oxy]oxane-2-carboxylic acid
SMILES (Canonical) COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C4=C(C=C3O2)OCO4)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O
SMILES (Isomeric) COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C4=C(C=C3O2)OCO4)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O
InChI InChI=1S/C23H20O14/c1-32-9-3-2-7(4-8(9)24)18-20(36-23-17(29)15(27)16(28)21(37-23)22(30)31)14(26)12-10(35-18)5-11-19(13(12)25)34-6-33-11/h2-5,15-17,21,23-25,27-29H,6H2,1H3,(H,30,31)
InChI Key ZPQIJJKOFIOFNV-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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There are no found synonyms.

2D Structure

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2D Structure of 3,3',5-Trihydroxy-4'-methoxy-6,7-methylenedioxyflavone 3-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 - 0.8714 87.14%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7109 71.09%
OATP2B1 inhibitior - 0.5507 55.07%
OATP1B1 inhibitior + 0.9464 94.64%
OATP1B3 inhibitior + 0.9716 97.16%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7639 76.39%
P-glycoprotein inhibitior - 0.4925 49.25%
P-glycoprotein substrate - 0.7004 70.04%
CYP3A4 substrate + 0.6403 64.03%
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 + 0.8497 84.97%
CYP inhibitory promiscuity + 0.6490 64.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5299 52.99%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.8834 88.34%
Skin irritation - 0.7653 76.53%
Skin corrosion - 0.9319 93.19%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6778 67.78%
Micronuclear + 0.8274 82.74%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8730 87.30%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.9332 93.32%
Acute Oral Toxicity (c) III 0.6759 67.59%
Estrogen receptor binding + 0.7860 78.60%
Androgen receptor binding + 0.6847 68.47%
Thyroid receptor binding - 0.5526 55.26%
Glucocorticoid receptor binding + 0.7052 70.52%
Aromatase binding - 0.5122 51.22%
PPAR gamma + 0.5884 58.84%
Honey bee toxicity - 0.7612 76.12%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7000 70.00%
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 98.83% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.74% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.19% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.42% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.18% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.87% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.28% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.59% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.51% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.61% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 90.08% 91.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.22% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.32% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.17% 99.15%
CHEMBL3194 P02766 Transthyretin 85.62% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.17% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.81% 99.23%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.37% 95.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.61% 95.89%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 83.51% 95.64%
CHEMBL3401 O75469 Pregnane X receptor 82.96% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.75% 96.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 81.46% 95.53%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.00% 95.50%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 80.26% 82.67%
CHEMBL4208 P20618 Proteasome component C5 80.14% 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.
Spinacia oleracea

Cross-Links

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PubChem 85388342
LOTUS LTS0099246
wikiData Q105381120