Formononetin 7-O-glucoside-6''-O-malonate

Details

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Internal ID 9a0ccea1-1565-4dbe-823d-813194ed160b
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavonoid O-glycosides
IUPAC Name 3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid
SMILES (Canonical) COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)COC(=O)CC(=O)O)O)O)O
InChI InChI=1S/C25H24O12/c1-33-13-4-2-12(3-5-13)16-10-34-17-8-14(6-7-15(17)21(16)29)36-25-24(32)23(31)22(30)18(37-25)11-35-20(28)9-19(26)27/h2-8,10,18,22-25,30-32H,9,11H2,1H3,(H,26,27)/t18-,22-,23+,24-,25-/m1/s1
InChI Key RDTAGQKYPGLCBK-GOZZSVHWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H24O12
Molecular Weight 516.40 g/mol
Exact Mass 516.12677620 g/mol
Topological Polar Surface Area (TPSA) 178.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.67
H-Bond Acceptor 11
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

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CHEBI:80389
6'-Malonyl Ononin
CHEMBL3426808
DTXSID801259044
Formononetin 7-(6-O-malonylglucoside)
Formononetin-7-O-beta-D-glucoside-6-O-malonate
Q27149411
7-hydroxy-4'-methoxyisoflavone 7-O-beta-(6'-O-malonylglucoside)
3-(4-methoxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 6-O-(carboxyacetyl)-beta-D-glucopyranoside
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid

2D Structure

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2D Structure of Formononetin 7-O-glucoside-6''-O-malonate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4650 46.50%
Caco-2 - 0.8716 87.16%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6150 61.50%
OATP2B1 inhibitior - 0.8353 83.53%
OATP1B1 inhibitior + 0.9211 92.11%
OATP1B3 inhibitior + 0.9628 96.28%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7454 74.54%
P-glycoprotein inhibitior + 0.5825 58.25%
P-glycoprotein substrate - 0.7746 77.46%
CYP3A4 substrate + 0.6454 64.54%
CYP2C9 substrate - 0.8113 81.13%
CYP2D6 substrate - 0.8567 85.67%
CYP3A4 inhibition - 0.8782 87.82%
CYP2C9 inhibition - 0.9310 93.10%
CYP2C19 inhibition - 0.9222 92.22%
CYP2D6 inhibition - 0.9310 93.10%
CYP1A2 inhibition - 0.9104 91.04%
CYP2C8 inhibition + 0.5630 56.30%
CYP inhibitory promiscuity - 0.9238 92.38%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6500 65.00%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9263 92.63%
Skin irritation - 0.8282 82.82%
Skin corrosion - 0.9516 95.16%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3679 36.79%
Micronuclear + 0.6918 69.18%
Hepatotoxicity - 0.5766 57.66%
skin sensitisation - 0.9297 92.97%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8721 87.21%
Acute Oral Toxicity (c) III 0.6607 66.07%
Estrogen receptor binding + 0.8349 83.49%
Androgen receptor binding + 0.7014 70.14%
Thyroid receptor binding - 0.5161 51.61%
Glucocorticoid receptor binding + 0.6915 69.15%
Aromatase binding + 0.5315 53.15%
PPAR gamma + 0.7219 72.19%
Honey bee toxicity - 0.8805 88.05%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9093 90.93%

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 99.05% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.06% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.42% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.68% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.49% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.96% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.86% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.87% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.77% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.62% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.73% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.47% 86.33%
CHEMBL220 P22303 Acetylcholinesterase 86.70% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.80% 95.50%
CHEMBL5255 O00206 Toll-like receptor 4 82.81% 92.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.63% 94.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.05% 95.89%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.21% 87.67%

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.
Astragalus mongholicus
Glycyrrhiza pallidiflora
Maackia amurensis
Medicago sativa
Medicago truncatula
Pueraria montana var. lobata

Cross-Links

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PubChem 23724663
NPASS NPC305741
LOTUS LTS0275484
wikiData Q27149411