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

Details

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Internal ID 2e52f084-3598-440a-88b8-7b2327eec5e5
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 7-[(2R,3S,4S,5R,6S)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H30O14/c1-10-20(32)21(33)23(35)26(37-10)41-25-18(9-28)40-27(24(36)22(25)34)38-13-6-14(30)19-15(31)8-16(39-17(19)7-13)11-2-4-12(29)5-3-11/h2-8,10,18,20-30,32-36H,9H2,1H3/t10-,18+,20-,21+,22+,23+,24+,25+,26+,27+/m1/s1
InChI Key OGGOZTAYPXBKCH-FFUDPDCJSA-N
Popularity 3 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 -0.80
Atomic LogP (AlogP) -1.10
H-Bond Acceptor 14
H-Bond Donor 8
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-[(2R,3S,4S,5R,6S)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-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 - 0.5193 51.93%
Caco-2 - 0.8996 89.96%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7135 71.35%
OATP2B1 inhibitior - 0.5625 56.25%
OATP1B1 inhibitior + 0.9397 93.97%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8199 81.99%
P-glycoprotein inhibitior - 0.7402 74.02%
P-glycoprotein substrate - 0.5636 56.36%
CYP3A4 substrate + 0.6171 61.71%
CYP2C9 substrate - 0.6986 69.86%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.8713 87.13%
CYP2C9 inhibition - 0.8929 89.29%
CYP2C19 inhibition - 0.9499 94.99%
CYP2D6 inhibition - 0.9496 94.96%
CYP1A2 inhibition - 0.8964 89.64%
CYP2C8 inhibition + 0.6642 66.42%
CYP inhibitory promiscuity - 0.6127 61.27%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6441 64.41%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9225 92.25%
Skin irritation - 0.8200 82.00%
Skin corrosion - 0.9658 96.58%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4144 41.44%
Micronuclear + 0.6233 62.33%
Hepatotoxicity - 0.8500 85.00%
skin sensitisation - 0.9324 93.24%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.9102 91.02%
Acute Oral Toxicity (c) III 0.6434 64.34%
Estrogen receptor binding + 0.7072 70.72%
Androgen receptor binding + 0.6586 65.86%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.4899 48.99%
Aromatase binding + 0.5497 54.97%
PPAR gamma + 0.7547 75.47%
Honey bee toxicity - 0.6281 62.81%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5350 53.50%
Fish aquatic toxicity + 0.7658 76.58%

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 99.39% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.82% 91.49%
CHEMBL2581 P07339 Cathepsin D 97.36% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.03% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.85% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.75% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 92.20% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.43% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.98% 99.15%
CHEMBL3194 P02766 Transthyretin 88.44% 90.71%
CHEMBL242 Q92731 Estrogen receptor beta 87.87% 98.35%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.81% 85.14%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.72% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.30% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.68% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.68% 91.71%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 85.09% 95.78%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.98% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.83% 90.71%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.49% 83.57%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.09% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.02% 96.21%

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.
Cirsium arvense
Lomelosia caucasica

Cross-Links

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PubChem 162891431
LOTUS LTS0068033
wikiData Q105191594