Lupinisoflavone C

Details

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Internal ID 76e4aa26-de70-4e5c-af14-f0ff81ffffac
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 5,7-dihydroxy-3-[2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H18O6/c1-20(2,24)17-6-11-5-10(3-4-15(11)26-17)13-9-25-16-8-12(21)7-14(22)18(16)19(13)23/h3-5,7-9,17,21-22,24H,6H2,1-2H3
InChI Key ASFWAKDAUOGISP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O6
Molecular Weight 354.40 g/mol
Exact Mass 354.11033829 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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LMPK12050182

2D Structure

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2D Structure of Lupinisoflavone C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9832 98.32%
Caco-2 - 0.5495 54.95%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8035 80.35%
OATP2B1 inhibitior + 0.5662 56.62%
OATP1B1 inhibitior + 0.9143 91.43%
OATP1B3 inhibitior + 0.9110 91.10%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5763 57.63%
P-glycoprotein inhibitior - 0.5714 57.14%
P-glycoprotein substrate - 0.7189 71.89%
CYP3A4 substrate + 0.6410 64.10%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.8170 81.70%
CYP3A4 inhibition + 0.5373 53.73%
CYP2C9 inhibition + 0.5392 53.92%
CYP2C19 inhibition - 0.5479 54.79%
CYP2D6 inhibition - 0.8337 83.37%
CYP1A2 inhibition - 0.6004 60.04%
CYP2C8 inhibition + 0.7157 71.57%
CYP inhibitory promiscuity - 0.5686 56.86%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5492 54.92%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.7712 77.12%
Skin irritation - 0.7241 72.41%
Skin corrosion - 0.8956 89.56%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6246 62.46%
Micronuclear + 0.5859 58.59%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8068 80.68%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.5750 57.50%
Acute Oral Toxicity (c) III 0.6533 65.33%
Estrogen receptor binding + 0.8943 89.43%
Androgen receptor binding + 0.7507 75.07%
Thyroid receptor binding + 0.6863 68.63%
Glucocorticoid receptor binding + 0.7771 77.71%
Aromatase binding + 0.8315 83.15%
PPAR gamma + 0.8718 87.18%
Honey bee toxicity - 0.8394 83.94%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9473 94.73%

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
CHEMBL2581 P07339 Cathepsin D 98.54% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.35% 91.11%
CHEMBL1929 P47989 Xanthine dehydrogenase 97.47% 96.12%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.68% 89.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 93.58% 95.78%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.85% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.56% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.02% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 89.25% 94.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 89.22% 95.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.92% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 85.87% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.43% 85.14%
CHEMBL242 Q92731 Estrogen receptor beta 83.36% 98.35%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.18% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.63% 99.23%
CHEMBL3194 P02766 Transthyretin 82.52% 90.71%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.96% 93.04%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.49% 93.65%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.41% 99.15%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.83% 100.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.37% 95.53%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.10% 97.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.01% 93.40%

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.
Lupinus albus

Cross-Links

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PubChem 44257284
LOTUS LTS0273865
wikiData Q104917804