Kaempferide 7-glucoside

Details

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Internal ID da618ce9-fa16-47eb-b3b8-deced165787b
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 3,5-dihydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SMILES (Canonical) COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O
InChI InChI=1S/C22H22O11/c1-30-10-4-2-9(3-5-10)21-19(28)17(26)15-12(24)6-11(7-13(15)32-21)31-22-20(29)18(27)16(25)14(8-23)33-22/h2-7,14,16,18,20,22-25,27-29H,8H2,1H3/t14-,16-,18+,20-,22-/m1/s1
InChI Key XJQKYCNSLNPXDD-XMHBHJPISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O11
Molecular Weight 462.40 g/mol
Exact Mass 462.11621151 g/mol
Topological Polar Surface Area (TPSA) 175.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.06
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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kaempferide 7-glucoside
kaempferide 7-O-glucoside
16290-08-7
UX5577J266
7-((2R,3S,4R,5S,6S)-6-(Hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl)oxy-2-(4-methoxyphenyl)-3,5-bis(oxidanyl)chromen-4-one
UNII-UX5577J266
CHEBI:187181
DTXSID901312691
Kaempferide 7-o-beta-D-glucopyranoside
KAEMPFERIDE 7-O-.BETA.-D-GLUCOPYRANOSIDE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Kaempferide 7-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4855 48.55%
Caco-2 - 0.9151 91.51%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6190 61.90%
OATP2B1 inhibitior + 0.5911 59.11%
OATP1B1 inhibitior + 0.9040 90.40%
OATP1B3 inhibitior + 0.9740 97.40%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6796 67.96%
P-glycoprotein inhibitior - 0.7103 71.03%
P-glycoprotein substrate - 0.6855 68.55%
CYP3A4 substrate + 0.6324 63.24%
CYP2C9 substrate - 0.8485 84.85%
CYP2D6 substrate - 0.8501 85.01%
CYP3A4 inhibition - 0.9108 91.08%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9173 91.73%
CYP2D6 inhibition - 0.9514 95.14%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition + 0.7807 78.07%
CYP inhibitory promiscuity - 0.7292 72.92%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6890 68.90%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.8682 86.82%
Skin irritation - 0.8153 81.53%
Skin corrosion - 0.9600 96.00%
Ames mutagenesis + 0.6736 67.36%
Human Ether-a-go-go-Related Gene inhibition - 0.3665 36.65%
Micronuclear + 0.6633 66.33%
Hepatotoxicity - 0.7448 74.48%
skin sensitisation - 0.9373 93.73%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8999 89.99%
Acute Oral Toxicity (c) III 0.6624 66.24%
Estrogen receptor binding + 0.7974 79.74%
Androgen receptor binding + 0.6828 68.28%
Thyroid receptor binding + 0.5773 57.73%
Glucocorticoid receptor binding + 0.6999 69.99%
Aromatase binding + 0.6457 64.57%
PPAR gamma + 0.7761 77.61%
Honey bee toxicity - 0.8272 82.72%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.7079 70.79%

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%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.11% 94.00%
CHEMBL2581 P07339 Cathepsin D 96.43% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 96.17% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.93% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.99% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.99% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.28% 99.15%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 93.04% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 90.92% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.75% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.72% 95.56%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 90.07% 95.64%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.70% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.35% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.89% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.76% 94.45%
CHEMBL4208 P20618 Proteasome component C5 83.79% 90.00%
CHEMBL1907 P15144 Aminopeptidase N 82.06% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.92% 96.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.86% 97.36%

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.
Klasea centauroides subsp. strangulata
Prunus davidiana
Prunus mume
Pterospermum acerifolium

Cross-Links

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PubChem 90657201
NPASS NPC71531
LOTUS LTS0104749
wikiData Q105329140