(3S)-5-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-3-methyl-5-oxopentanoic acid

Details

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Internal ID d3039ed1-ed49-48df-bea2-75ad67fe19a1
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name (3S)-5-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-3-methyl-5-oxopentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H38O21/c1-33(48,7-20(38)39)8-21(40)49-10-19-24(42)27(45)28(46)31(53-19)51-17-6-16-22(14(37)5-15(50-16)11-2-3-12(35)13(36)4-11)25(43)30(17)54-32-29(47)26(44)23(41)18(9-34)52-32/h2-6,18-19,23-24,26-29,31-32,34-36,41-48H,7-10H2,1H3,(H,38,39)/t18-,19+,23+,24+,26-,27-,28+,29+,31+,32-,33-/m0/s1
InChI Key FIZMLXFRUFYIEH-AICJJEHTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C33H38O21
Molecular Weight 770.60 g/mol
Exact Mass 770.19055822 g/mol
Topological Polar Surface Area (TPSA) 349.00 Ų
XlogP -2.60
Atomic LogP (AlogP) -2.90
H-Bond Acceptor 20
H-Bond Donor 12
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S)-5-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-3-methyl-5-oxopentanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5510 55.10%
Caco-2 - 0.8871 88.71%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6254 62.54%
OATP2B1 inhibitior - 0.7148 71.48%
OATP1B1 inhibitior + 0.8125 81.25%
OATP1B3 inhibitior + 0.9583 95.83%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6521 65.21%
P-glycoprotein inhibitior + 0.6542 65.42%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6667 66.67%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.8738 87.38%
CYP3A4 inhibition - 0.8957 89.57%
CYP2C9 inhibition - 0.9296 92.96%
CYP2C19 inhibition - 0.8779 87.79%
CYP2D6 inhibition - 0.9469 94.69%
CYP1A2 inhibition - 0.8741 87.41%
CYP2C8 inhibition + 0.7691 76.91%
CYP inhibitory promiscuity - 0.9446 94.46%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6009 60.09%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9090 90.90%
Skin irritation - 0.8295 82.95%
Skin corrosion - 0.9498 94.98%
Ames mutagenesis - 0.5764 57.64%
Human Ether-a-go-go-Related Gene inhibition + 0.6680 66.80%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.9133 91.33%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.9576 95.76%
Acute Oral Toxicity (c) III 0.5736 57.36%
Estrogen receptor binding + 0.8074 80.74%
Androgen receptor binding + 0.6501 65.01%
Thyroid receptor binding - 0.5188 51.88%
Glucocorticoid receptor binding + 0.5743 57.43%
Aromatase binding + 0.6318 63.18%
PPAR gamma + 0.7306 73.06%
Honey bee toxicity - 0.7245 72.45%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6849 68.49%
Fish aquatic toxicity + 0.9470 94.70%

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 99.74% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.38% 85.14%
CHEMBL220 P22303 Acetylcholinesterase 98.62% 94.45%
CHEMBL2581 P07339 Cathepsin D 98.11% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.84% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.83% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.50% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.44% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 91.62% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 91.47% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.78% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.91% 86.92%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.86% 96.09%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 87.50% 95.64%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 87.21% 80.78%
CHEMBL3194 P02766 Transthyretin 85.54% 90.71%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.94% 96.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.91% 95.56%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.22% 96.90%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.49% 97.09%

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.
Frullania teneriffae

Cross-Links

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PubChem 163067844
LOTUS LTS0079935
wikiData Q104995937