Formononetin 7-O-apiosyl-(1->2)-glucoside

Details

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Internal ID fb7dd6b4-9ad9-4a89-94cc-4d32aca5ac10
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavonoid O-glycosides
IUPAC Name 7-[3-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(4-methoxyphenyl)chromen-4-one
SMILES (Canonical) COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)OC5C(C(CO5)(CO)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)OC5C(C(CO5)(CO)O)O
InChI InChI=1S/C27H30O13/c1-35-14-4-2-13(3-5-14)17-10-36-18-8-15(6-7-16(18)20(17)30)38-25-23(22(32)21(31)19(9-28)39-25)40-26-24(33)27(34,11-29)12-37-26/h2-8,10,19,21-26,28-29,31-34H,9,11-12H2,1H3
InChI Key TUUBGLDJKKCMRH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O13
Molecular Weight 562.50 g/mol
Exact Mass 562.16864101 g/mol
Topological Polar Surface Area (TPSA) 194.00 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.89
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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LMPK12050024

2D Structure

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2D Structure of Formononetin 7-O-apiosyl-(1->2)-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6754 67.54%
Caco-2 - 0.8884 88.84%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6254 62.54%
OATP2B1 inhibitior - 0.8417 84.17%
OATP1B1 inhibitior + 0.9253 92.53%
OATP1B3 inhibitior + 0.9655 96.55%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7841 78.41%
P-glycoprotein inhibitior - 0.4935 49.35%
P-glycoprotein substrate - 0.6422 64.22%
CYP3A4 substrate + 0.6940 69.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8359 83.59%
CYP3A4 inhibition - 0.8418 84.18%
CYP2C9 inhibition - 0.8860 88.60%
CYP2C19 inhibition - 0.8296 82.96%
CYP2D6 inhibition - 0.9113 91.13%
CYP1A2 inhibition - 0.9060 90.60%
CYP2C8 inhibition + 0.4824 48.24%
CYP inhibitory promiscuity - 0.7811 78.11%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5250 52.50%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9397 93.97%
Skin irritation - 0.8131 81.31%
Skin corrosion - 0.9457 94.57%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7375 73.75%
Micronuclear + 0.6733 67.33%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8821 88.21%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7109 71.09%
Acute Oral Toxicity (c) III 0.6985 69.85%
Estrogen receptor binding + 0.8238 82.38%
Androgen receptor binding + 0.7236 72.36%
Thyroid receptor binding + 0.5518 55.18%
Glucocorticoid receptor binding + 0.6279 62.79%
Aromatase binding + 0.6740 67.40%
PPAR gamma + 0.7899 78.99%
Honey bee toxicity - 0.7569 75.69%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.6644 66.44%

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 99.46% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.32% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 96.27% 95.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.79% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.70% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.30% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.59% 86.92%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.50% 97.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.89% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.43% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.88% 96.09%
CHEMBL3922 P50579 Methionine aminopeptidase 2 89.89% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.27% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.07% 86.33%
CHEMBL4302 P08183 P-glycoprotein 1 87.80% 92.98%
CHEMBL1907 P15144 Aminopeptidase N 85.59% 93.31%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.35% 94.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.97% 96.77%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.88% 97.36%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 83.20% 95.53%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.90% 95.83%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.89% 99.23%
CHEMBL4208 P20618 Proteasome component C5 82.52% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.38% 92.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.91% 97.14%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.07% 95.71%

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.
Glycyrrhiza aspera
Glycyrrhiza glabra
Glycyrrhiza inflata
Glycyrrhiza uralensis
Spatholobus suberectus

Cross-Links

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PubChem 44257223
NPASS NPC51558