7-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one

Details

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Internal ID 92523705-d224-4acd-bba7-780d228b7315
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 7-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H30O16/c28-7-17-20(34)22(36)23(37)26(41-17)43-25-21(35)18(8-29)42-27(24(25)38)39-10-4-13(32)19-14(33)6-15(40-16(19)5-10)9-1-2-11(30)12(31)3-9/h1-6,17-18,20-32,34-38H,7-8H2/t17-,18-,20-,21-,22+,23-,24-,25+,26+,27-/m0/s1
InChI Key IVYJGRDQTLLOCO-FDUKAQDMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O16
Molecular Weight 610.50 g/mol
Exact Mass 610.15338487 g/mol
Topological Polar Surface Area (TPSA) 266.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -2.42
H-Bond Acceptor 16
H-Bond Donor 10
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-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 - 0.5736 57.36%
Caco-2 - 0.9245 92.45%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.5848 58.48%
OATP2B1 inhibitior - 0.5575 55.75%
OATP1B1 inhibitior + 0.9547 95.47%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6143 61.43%
P-glycoprotein inhibitior - 0.6664 66.64%
P-glycoprotein substrate - 0.7275 72.75%
CYP3A4 substrate + 0.5986 59.86%
CYP2C9 substrate - 0.6709 67.09%
CYP2D6 substrate - 0.8582 85.82%
CYP3A4 inhibition - 0.9390 93.90%
CYP2C9 inhibition - 0.9315 93.15%
CYP2C19 inhibition - 0.9047 90.47%
CYP2D6 inhibition - 0.9458 94.58%
CYP1A2 inhibition - 0.9180 91.80%
CYP2C8 inhibition + 0.7241 72.41%
CYP inhibitory promiscuity - 0.7526 75.26%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6848 68.48%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9073 90.73%
Skin irritation - 0.8255 82.55%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis + 0.6136 61.36%
Human Ether-a-go-go-Related Gene inhibition + 0.7269 72.69%
Micronuclear + 0.6433 64.33%
Hepatotoxicity - 0.8821 88.21%
skin sensitisation - 0.9132 91.32%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8344 83.44%
Acute Oral Toxicity (c) IV 0.4763 47.63%
Estrogen receptor binding + 0.7727 77.27%
Androgen receptor binding + 0.6708 67.08%
Thyroid receptor binding + 0.5265 52.65%
Glucocorticoid receptor binding - 0.5549 55.49%
Aromatase binding + 0.6088 60.88%
PPAR gamma + 0.7748 77.48%
Honey bee toxicity - 0.6159 61.59%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5950 59.50%
Fish aquatic toxicity + 0.7958 79.58%

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 99.72% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.40% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.55% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.27% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.13% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.77% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.54% 86.92%
CHEMBL3194 P02766 Transthyretin 90.55% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.06% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 88.66% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.57% 94.45%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 87.50% 83.57%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.37% 97.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 86.38% 95.78%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.80% 96.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.81% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.18% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.50% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.76% 90.71%

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.
Colchicum speciosum

Cross-Links

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PubChem 163193092
LOTUS LTS0175763
wikiData Q105121384