5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl 2-O-(4-(((3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl)oxy)methyl)-3,4-dihydroxyoxolan-2-yl)hexopyranoside

Details

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Internal ID ceefdc6b-0588-4eeb-94cd-e11659b934e8
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 7-[3-[4-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H40O19/c1-44-19-4-13(2-3-15(19)35)18-7-17(37)22-16(36)5-14(6-20(22)49-18)48-28-25(24(39)23(38)21(8-33)50-28)51-30-27(41)32(43,12-47-30)11-46-29-26(40)31(42,9-34)10-45-29/h2-6,18,21,23-30,33-36,38-43H,7-12H2,1H3
InChI Key HUBUCUOTSSVULF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H40O19
Molecular Weight 728.60 g/mol
Exact Mass 728.21637904 g/mol
Topological Polar Surface Area (TPSA) 293.00 Ų
XlogP -2.40
Atomic LogP (AlogP) -3.08
H-Bond Acceptor 19
H-Bond Donor 10
Rotatable Bonds 11

Synonyms

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119016-92-1
7-[3-[4-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one
DTXSID80922852
Homoeriodictyol-7-apiosyl(1-5)-apiosyl(1-2)-glucopyranoside
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl 2-O-[4-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4-dihydroxyoxolan-2-yl]hexopyranoside

2D Structure

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2D Structure of 5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl 2-O-(4-(((3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl)oxy)methyl)-3,4-dihydroxyoxolan-2-yl)hexopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6999 69.99%
Caco-2 - 0.8916 89.16%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6762 67.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9036 90.36%
OATP1B3 inhibitior + 0.9628 96.28%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7424 74.24%
P-glycoprotein inhibitior + 0.6467 64.67%
P-glycoprotein substrate + 0.5405 54.05%
CYP3A4 substrate + 0.7043 70.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8457 84.57%
CYP3A4 inhibition - 0.8688 86.88%
CYP2C9 inhibition - 0.8938 89.38%
CYP2C19 inhibition - 0.8148 81.48%
CYP2D6 inhibition - 0.9092 90.92%
CYP1A2 inhibition - 0.9115 91.15%
CYP2C8 inhibition + 0.6849 68.49%
CYP inhibitory promiscuity - 0.8358 83.58%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5632 56.32%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.9131 91.31%
Skin irritation - 0.8179 81.79%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7424 74.24%
Micronuclear + 0.5774 57.74%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8789 87.89%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.4863 48.63%
Acute Oral Toxicity (c) III 0.6243 62.43%
Estrogen receptor binding + 0.7937 79.37%
Androgen receptor binding + 0.5545 55.45%
Thyroid receptor binding - 0.5133 51.33%
Glucocorticoid receptor binding + 0.5767 57.67%
Aromatase binding + 0.6342 63.42%
PPAR gamma + 0.7182 71.82%
Honey bee toxicity - 0.6526 65.26%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.7753 77.53%

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 99.80% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.78% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.74% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.64% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.14% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.83% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.77% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 94.17% 86.92%
CHEMBL2581 P07339 Cathepsin D 92.63% 98.95%
CHEMBL4208 P20618 Proteasome component C5 92.44% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.39% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.32% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.09% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.74% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.74% 96.21%
CHEMBL226 P30542 Adenosine A1 receptor 88.58% 95.93%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.45% 96.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.17% 97.36%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.07% 97.14%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.39% 85.14%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.37% 91.07%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.12% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.93% 99.17%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 80.78% 92.88%
CHEMBL4581 P52732 Kinesin-like protein 1 80.64% 93.18%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.24% 100.00%

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.
Viscum angulatum

Cross-Links

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PubChem 195288
LOTUS LTS0258766
wikiData Q82896602