Biochanin A 7-(6-malonylglucoside)

Details

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Internal ID 10280e60-81bf-47c6-a198-4b15aa1ba272
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavonoid O-glycosides
IUPAC Name 3-oxo-3-[[3,4,5-trihydroxy-6-[5-hydroxy-3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid
SMILES (Canonical) COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O
InChI InChI=1S/C25H24O13/c1-34-12-4-2-11(3-5-12)14-9-35-16-7-13(6-15(26)20(16)21(14)30)37-25-24(33)23(32)22(31)17(38-25)10-36-19(29)8-18(27)28/h2-7,9,17,22-26,31-33H,8,10H2,1H3,(H,27,28)
InChI Key VRCBYTZZZFFKEN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H24O13
Molecular Weight 532.40 g/mol
Exact Mass 532.12169082 g/mol
Topological Polar Surface Area (TPSA) 199.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.38
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

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Biochanin A 7-O-beta-D-glucoside-6''-O-malonate
CHEBI:190739
Isoflavone base + 2O + 1MeO, O-MalonylHex
3-oxo-3-[[3,4,5-trihydroxy-6-[5-hydroxy-3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid

2D Structure

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2D Structure of Biochanin A 7-(6-malonylglucoside)

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 - 0.8862 88.62%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6150 61.50%
OATP2B1 inhibitior - 0.6969 69.69%
OATP1B1 inhibitior + 0.9230 92.30%
OATP1B3 inhibitior + 0.9628 96.28%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7828 78.28%
P-glycoprotein inhibitior - 0.4435 44.35%
P-glycoprotein substrate - 0.7291 72.91%
CYP3A4 substrate + 0.6477 64.77%
CYP2C9 substrate - 0.6278 62.78%
CYP2D6 substrate - 0.8638 86.38%
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 + 0.6893 68.93%
CYP inhibitory promiscuity - 0.9238 92.38%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6500 65.00%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9059 90.59%
Skin irritation - 0.8282 82.82%
Skin corrosion - 0.9516 95.16%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6561 65.61%
Micronuclear + 0.6918 69.18%
Hepatotoxicity - 0.6573 65.73%
skin sensitisation - 0.9297 92.97%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8222 82.22%
Acute Oral Toxicity (c) III 0.6607 66.07%
Estrogen receptor binding + 0.8379 83.79%
Androgen receptor binding + 0.6802 68.02%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7036 70.36%
Aromatase binding + 0.5668 56.68%
PPAR gamma + 0.7215 72.15%
Honey bee toxicity - 0.8571 85.71%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6700 67.00%
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 99.24% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.62% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.31% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.87% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.66% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.63% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.89% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.66% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.68% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.56% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.02% 95.56%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 88.63% 95.64%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.24% 96.00%
CHEMBL220 P22303 Acetylcholinesterase 85.68% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.08% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 83.89% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.90% 94.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.10% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.06% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 80.78% 92.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.73% 99.23%
CHEMBL226 P30542 Adenosine A1 receptor 80.69% 95.93%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.51% 94.00%
CHEMBL4208 P20618 Proteasome component C5 80.44% 90.00%

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.
Cicer arietinum
Pueraria montana var. lobata
Trifolium pratense
Trifolium subterraneum

Cross-Links

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PubChem 131751062
LOTUS LTS0115760
wikiData Q104389712