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7-[3,5-Dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

Table of Contents

Details
Physical and Chemical Properties
Synonyms
2D Structure
3D Structure
ADMET Properties
Targets (proven and/or predicted)
Plants that contains it
Cross-Links

Details

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Internal ID 366343e5-5473-4a48-b6aa-4760c1c06cdb
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 7-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)C6=CC=C(C=C6)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)C6=CC=C(C=C6)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)O
InChI InChI=1S/C39H50O25/c1-11-21(44)34(63-37-30(53)27(50)23(46)18(9-41)61-37)32(55)39(57-11)58-14-6-15(43)20-16(7-14)59-33(12-2-4-13(42)5-3-12)35(25(20)48)64-38-31(54)28(51)24(47)19(62-38)10-56-36-29(52)26(49)22(45)17(8-40)60-36/h2-7,11,17-19,21-24,26-32,34,36-47,49-55H,8-10H2,1H3
InChI Key FOQDUKUEWRKMCX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C39H50O25
Molecular Weight 918.80 g/mol
Exact Mass 918.26411708 g/mol
Topological Polar Surface Area (TPSA) 404.00 Ų
XlogP -4.30
Atomic LogP (AlogP) -6.10
H-Bond Acceptor 25
H-Bond Donor 15
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-[3,5-Dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5372 53.72%
Caco-2 - 0.8856 88.56%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6684 66.84%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.8976 89.76%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9139 91.39%
P-glycoprotein inhibitior + 0.6587 65.87%
P-glycoprotein substrate + 0.5822 58.22%
CYP3A4 substrate + 0.6551 65.51%
CYP2C9 substrate - 0.6986 69.86%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.9550 95.50%
CYP2C9 inhibition - 0.9252 92.52%
CYP2C19 inhibition - 0.9129 91.29%
CYP2D6 inhibition - 0.9613 96.13%
CYP1A2 inhibition - 0.8948 89.48%
CYP2C8 inhibition + 0.7719 77.19%
CYP inhibitory promiscuity - 0.6991 69.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6759 67.59%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.9027 90.27%
Skin irritation - 0.8374 83.74%
Skin corrosion - 0.9635 96.35%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8421 84.21%
Micronuclear + 0.6333 63.33%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.9289 92.89%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8314 83.14%
Acute Oral Toxicity (c) III 0.5567 55.67%
Estrogen receptor binding + 0.8118 81.18%
Androgen receptor binding + 0.6000 60.00%
Thyroid receptor binding + 0.5449 54.49%
Glucocorticoid receptor binding - 0.4747 47.47%
Aromatase binding + 0.5224 52.24%
PPAR gamma + 0.7374 73.74%
Honey bee toxicity - 0.7198 71.98%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5250 52.50%
Fish aquatic toxicity + 0.8024 80.24%

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 99.50% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.24% 91.49%
CHEMBL2581 P07339 Cathepsin D 97.43% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.38% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.32% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.13% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 92.88% 94.73%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 92.07% 95.64%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.80% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.03% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.46% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.05% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.95% 97.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 85.66% 95.78%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.86% 95.56%
CHEMBL242 Q92731 Estrogen receptor beta 84.66% 98.35%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.55% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.42% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.05% 95.89%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.57% 94.80%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.48% 97.36%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 80.03% 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.
Cardamine leucantha

Cross-Links

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PubChem 162985737
LOTUS LTS0087441
wikiData Q104998887