quercetin-6-C-glucoside

Details

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Internal ID 77908e52-f169-4610-9d43-53b6af851263
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid C-glycosides
IUPAC Name 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H20O12/c22-5-11-14(26)17(29)19(31)21(33-11)12-9(25)4-10-13(15(12)27)16(28)18(30)20(32-10)6-1-2-7(23)8(24)3-6/h1-4,11,14,17,19,21-27,29-31H,5H2/t11-,14-,17+,19-,21+/m1/s1
InChI Key IDPMRJRWHIXCDU-DSTJRUDUSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O12
Molecular Weight 464.40 g/mol
Exact Mass 464.09547607 g/mol
Topological Polar Surface Area (TPSA) 218.00 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.50
H-Bond Acceptor 12
H-Bond Donor 9
Rotatable Bonds 3

Synonyms

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SCHEMBL1773260

2D Structure

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2D Structure of quercetin-6-C-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6665 66.65%
Caco-2 - 0.9375 93.75%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5728 57.28%
OATP2B1 inhibitior + 0.5966 59.66%
OATP1B1 inhibitior + 0.8914 89.14%
OATP1B3 inhibitior + 0.9709 97.09%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4897 48.97%
P-glycoprotein inhibitior - 0.6597 65.97%
P-glycoprotein substrate - 0.7987 79.87%
CYP3A4 substrate + 0.5914 59.14%
CYP2C9 substrate - 0.6301 63.01%
CYP2D6 substrate - 0.8452 84.52%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9240 92.40%
CYP2D6 inhibition - 0.9476 94.76%
CYP1A2 inhibition - 0.8355 83.55%
CYP2C8 inhibition + 0.8207 82.07%
CYP inhibitory promiscuity - 0.7806 78.06%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7252 72.52%
Eye corrosion - 0.9936 99.36%
Eye irritation - 0.7986 79.86%
Skin irritation - 0.7691 76.91%
Skin corrosion - 0.9606 96.06%
Ames mutagenesis + 0.6629 66.29%
Human Ether-a-go-go-Related Gene inhibition - 0.4828 48.28%
Micronuclear + 0.6559 65.59%
Hepatotoxicity - 0.5321 53.21%
skin sensitisation - 0.8683 86.83%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.9173 91.73%
Acute Oral Toxicity (c) IV 0.3746 37.46%
Estrogen receptor binding + 0.6754 67.54%
Androgen receptor binding + 0.7172 71.72%
Thyroid receptor binding + 0.5986 59.86%
Glucocorticoid receptor binding + 0.6683 66.83%
Aromatase binding - 0.4886 48.86%
PPAR gamma + 0.7360 73.60%
Honey bee toxicity - 0.7671 76.71%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.6921 69.21%

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 99.65% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.79% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.18% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.66% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.97% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 89.35% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.44% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 88.43% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.91% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.43% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.75% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.20% 86.92%

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.
Ulmus wallichiana

Cross-Links

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PubChem 21676320
LOTUS LTS0117311
wikiData Q105111450