3-[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

Details

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Internal ID 93c7f6ea-fa71-4697-9108-51f2a31951b4
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 3-[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H30O14/c1-9-17(31)20(34)22(36)26(37-9)41-25-21(35)18(32)10(2)38-27(25)40-24-19(33)16-14(30)7-13(29)8-15(16)39-23(24)11-3-5-12(28)6-4-11/h3-10,17-18,20-22,25-32,34-36H,1-2H3/t9-,10-,17-,18-,20-,21+,22-,25-,26-,27-/m0/s1
InChI Key IJXRVZWYGGTCEE-MBTABASWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O14
Molecular Weight 578.50 g/mol
Exact Mass 578.16355563 g/mol
Topological Polar Surface Area (TPSA) 225.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.37
H-Bond Acceptor 14
H-Bond Donor 8
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-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 + 0.8072 80.72%
Caco-2 - 0.8784 87.84%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7235 72.35%
OATP2B1 inhibitior - 0.5560 55.60%
OATP1B1 inhibitior + 0.8982 89.82%
OATP1B3 inhibitior + 0.8556 85.56%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8760 87.60%
P-glycoprotein inhibitior - 0.5716 57.16%
P-glycoprotein substrate - 0.5179 51.79%
CYP3A4 substrate + 0.6473 64.73%
CYP2C9 substrate - 0.7354 73.54%
CYP2D6 substrate - 0.8607 86.07%
CYP3A4 inhibition - 0.6813 68.13%
CYP2C9 inhibition - 0.8866 88.66%
CYP2C19 inhibition - 0.8648 86.48%
CYP2D6 inhibition - 0.9418 94.18%
CYP1A2 inhibition - 0.6999 69.99%
CYP2C8 inhibition + 0.8407 84.07%
CYP inhibitory promiscuity - 0.5626 56.26%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6369 63.69%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.8896 88.96%
Skin irritation - 0.6827 68.27%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis + 0.5263 52.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5988 59.88%
Micronuclear + 0.9200 92.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.8967 89.67%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8141 81.41%
Acute Oral Toxicity (c) III 0.4830 48.30%
Estrogen receptor binding + 0.8018 80.18%
Androgen receptor binding + 0.7222 72.22%
Thyroid receptor binding + 0.6285 62.85%
Glucocorticoid receptor binding + 0.6920 69.20%
Aromatase binding + 0.5338 53.38%
PPAR gamma + 0.7364 73.64%
Honey bee toxicity - 0.7578 75.78%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5250 52.50%
Fish aquatic toxicity + 0.9566 95.66%

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 98.99% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.70% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 98.08% 89.00%
CHEMBL2581 P07339 Cathepsin D 96.68% 98.95%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 95.26% 95.64%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.46% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.99% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 92.20% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.52% 95.56%
CHEMBL3194 P02766 Transthyretin 88.00% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.39% 90.71%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 85.70% 95.78%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.23% 97.36%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.71% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.50% 99.15%
CHEMBL242 Q92731 Estrogen receptor beta 82.36% 98.35%
CHEMBL4208 P20618 Proteasome component C5 82.03% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.81% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.24% 96.09%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.87% 93.10%
CHEMBL4530 P00488 Coagulation factor XIII 80.50% 96.00%

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.
Epimedium sagittatum

Cross-Links

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PubChem 162896961
LOTUS LTS0018003
wikiData Q105114210