3-oxo-3-[[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-5-yl]oxyoxan-2-yl]methoxy]propanoic acid

Details

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Internal ID 59010006-633b-4fe7-9452-0b7d6d748a44
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides
IUPAC Name 3-oxo-3-[[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-5-yl]oxyoxan-2-yl]methoxy]propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H24O13/c1-34-13-6-16-21(14(27)8-15(36-16)11-2-4-12(26)5-3-11)17(7-13)37-25-24(33)23(32)22(31)18(38-25)10-35-20(30)9-19(28)29/h2-8,18,22-26,31-33H,9-10H2,1H3,(H,28,29)/t18-,22+,23+,24+,25-/m1/s1
InChI Key WZEYEVDCZWOQJH-FYOOOJEWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H24O13
Molecular Weight 532.40 g/mol
Exact Mass 532.12169082 g/mol
Topological Polar Surface Area (TPSA) 199.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.38
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-oxo-3-[[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-5-yl]oxyoxan-2-yl]methoxy]propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5000 50.00%
Caco-2 - 0.8926 89.26%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6616 66.16%
OATP2B1 inhibitior - 0.7018 70.18%
OATP1B1 inhibitior + 0.8574 85.74%
OATP1B3 inhibitior + 0.9660 96.60%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7943 79.43%
P-glycoprotein inhibitior + 0.6525 65.25%
P-glycoprotein substrate - 0.6076 60.76%
CYP3A4 substrate + 0.6255 62.55%
CYP2C9 substrate - 0.6285 62.85%
CYP2D6 substrate - 0.8563 85.63%
CYP3A4 inhibition - 0.8925 89.25%
CYP2C9 inhibition - 0.9426 94.26%
CYP2C19 inhibition - 0.9328 93.28%
CYP2D6 inhibition - 0.9274 92.74%
CYP1A2 inhibition - 0.9362 93.62%
CYP2C8 inhibition + 0.7520 75.20%
CYP inhibitory promiscuity - 0.9261 92.61%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5959 59.59%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9086 90.86%
Skin irritation - 0.8273 82.73%
Skin corrosion - 0.9537 95.37%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4424 44.24%
Micronuclear + 0.6818 68.18%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.9367 93.67%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8686 86.86%
Acute Oral Toxicity (c) III 0.6998 69.98%
Estrogen receptor binding + 0.8683 86.83%
Androgen receptor binding + 0.7503 75.03%
Thyroid receptor binding + 0.5400 54.00%
Glucocorticoid receptor binding + 0.7336 73.36%
Aromatase binding + 0.5693 56.93%
PPAR gamma + 0.6881 68.81%
Honey bee toxicity - 0.8114 81.14%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7449 74.49%
Fish aquatic toxicity + 0.8838 88.38%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.61% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.79% 91.11%
CHEMBL220 P22303 Acetylcholinesterase 95.68% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.39% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.47% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.60% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.87% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.81% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.27% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.14% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.86% 86.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.16% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.30% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.07% 96.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.00% 86.92%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.95% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 83.81% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 83.74% 94.73%
CHEMBL5255 O00206 Toll-like receptor 4 83.62% 92.50%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 83.43% 89.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.98% 95.89%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 80.34% 95.83%

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.
Equisetum arvense

Cross-Links

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PubChem 163014969
LOTUS LTS0090062
wikiData Q105323067