Lupinisoflavone M

Details

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Internal ID 774bca5c-4aa3-44eb-b464-7cf237745c60
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 6-prenylated isoflavanones
IUPAC Name 6-(2,3-dihydroxy-3-methylbutyl)-5,7-dihydroxy-3-[2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]chromen-4-one
SMILES (Canonical) CC(C)(C1CC2=C(O1)C=CC(=C2)C3=COC4=C(C3=O)C(=C(C(=C4)O)CC(C(C)(C)O)O)O)O
SMILES (Isomeric) CC(C)(C1CC2=C(O1)C=CC(=C2)C3=COC4=C(C3=O)C(=C(C(=C4)O)CC(C(C)(C)O)O)O)O
InChI InChI=1S/C25H28O8/c1-24(2,30)19(27)9-14-16(26)10-18-21(22(14)28)23(29)15(11-32-18)12-5-6-17-13(7-12)8-20(33-17)25(3,4)31/h5-7,10-11,19-20,26-28,30-31H,8-9H2,1-4H3
InChI Key IXEGNYHOJYAEHW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O8
Molecular Weight 456.50 g/mol
Exact Mass 456.17841785 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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CHEBI:185611
LMPK12050183
6-(2,3-dihydroxy-3-methylbutyl)-5,7-dihydroxy-3-[2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzouran-5-yl]chromen-4-one

2D Structure

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2D Structure of Lupinisoflavone M

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9723 97.23%
Caco-2 - 0.7822 78.22%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7107 71.07%
OATP2B1 inhibitior + 0.5725 57.25%
OATP1B1 inhibitior + 0.8978 89.78%
OATP1B3 inhibitior + 0.9379 93.79%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8146 81.46%
P-glycoprotein inhibitior + 0.5951 59.51%
P-glycoprotein substrate - 0.5750 57.50%
CYP3A4 substrate + 0.6481 64.81%
CYP2C9 substrate - 0.6054 60.54%
CYP2D6 substrate - 0.8128 81.28%
CYP3A4 inhibition - 0.8009 80.09%
CYP2C9 inhibition - 0.8365 83.65%
CYP2C19 inhibition - 0.8088 80.88%
CYP2D6 inhibition - 0.9033 90.33%
CYP1A2 inhibition - 0.7787 77.87%
CYP2C8 inhibition + 0.6876 68.76%
CYP inhibitory promiscuity - 0.7964 79.64%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5550 55.50%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.8809 88.09%
Skin irritation - 0.7397 73.97%
Skin corrosion - 0.9114 91.14%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6737 67.37%
Micronuclear + 0.5359 53.59%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8112 81.12%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8926 89.26%
Acute Oral Toxicity (c) III 0.5671 56.71%
Estrogen receptor binding + 0.8994 89.94%
Androgen receptor binding + 0.7230 72.30%
Thyroid receptor binding + 0.6833 68.33%
Glucocorticoid receptor binding + 0.8300 83.00%
Aromatase binding + 0.8114 81.14%
PPAR gamma + 0.8592 85.92%
Honey bee toxicity - 0.7316 73.16%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9392 93.92%

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 99.52% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.00% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.32% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.23% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.63% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.59% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.16% 89.34%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.46% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.88% 95.56%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 89.17% 95.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.69% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 86.93% 94.73%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 86.85% 95.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.69% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.83% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.40% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.54% 90.71%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.21% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.09% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 81.83% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.51% 92.62%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.22% 85.11%

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 14728998
LOTUS LTS0111350
wikiData Q105122095