Lupinalbin F

Details

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Internal ID 1bb2d17f-a402-413c-a21a-d93817484cda
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 6-prenylated isoflavanones
IUPAC Name 1,3,8-trihydroxy-2,7-bis(3-methylbut-2-enyl)-[1]benzofuro[2,3-b]chromen-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H24O6/c1-12(2)5-7-14-18(27)11-19-21(22(14)28)23(29)20-16-9-10-17(26)15(8-6-13(3)4)24(16)31-25(20)30-19/h5-6,9-11,26-28H,7-8H2,1-4H3
InChI Key WNJJWUYKQKUQED-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H24O6
Molecular Weight 420.50 g/mol
Exact Mass 420.15728848 g/mol
Topological Polar Surface Area (TPSA) 100.00 Ų
XlogP 7.00
Atomic LogP (AlogP) 5.83
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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1,3,8-trihydroxy-2,7-bis(3-methylbut-2-enyl)-(1)benzofuro(2,3-b)chromen-11-one
1,3,8-trihydroxy-2,7-bis(3-methylbut-2-enyl)-[1]benzofuro[2,3-b]chromen-11-one
RefChem:154337
121747-93-1
CHEBI:178576
LMPK12160006
1,3,8-trihydroxy-2,7-bis(3-methylbut-2-enyl)-[1]benzouro[2,3-b]chromen-11-one

2D Structure

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2D Structure of Lupinalbin F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 - 0.6149 61.49%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7330 73.30%
OATP2B1 inhibitior - 0.5584 55.84%
OATP1B1 inhibitior + 0.9240 92.40%
OATP1B3 inhibitior + 0.8893 88.93%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8687 86.87%
P-glycoprotein inhibitior - 0.4439 44.39%
P-glycoprotein substrate - 0.6890 68.90%
CYP3A4 substrate + 0.5274 52.74%
CYP2C9 substrate - 0.5755 57.55%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition - 0.6146 61.46%
CYP2C9 inhibition + 0.8555 85.55%
CYP2C19 inhibition + 0.7886 78.86%
CYP2D6 inhibition - 0.7761 77.61%
CYP1A2 inhibition + 0.7288 72.88%
CYP2C8 inhibition + 0.4934 49.34%
CYP inhibitory promiscuity + 0.8666 86.66%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4606 46.06%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.5939 59.39%
Skin irritation - 0.6835 68.35%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3765 37.65%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.7011 70.11%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8497 84.97%
Acute Oral Toxicity (c) III 0.4626 46.26%
Estrogen receptor binding + 0.9490 94.90%
Androgen receptor binding + 0.8360 83.60%
Thyroid receptor binding + 0.5889 58.89%
Glucocorticoid receptor binding + 0.8282 82.82%
Aromatase binding + 0.6986 69.86%
PPAR gamma + 0.9177 91.77%
Honey bee toxicity - 0.8509 85.09%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9961 99.61%

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 99.54% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.95% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.63% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.59% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 94.54% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 93.54% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.27% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.28% 95.56%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 88.92% 98.11%
CHEMBL3038469 P24941 CDK2/Cyclin A 85.40% 91.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.22% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.00% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.66% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.24% 99.15%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 82.73% 83.10%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.84% 90.71%
CHEMBL3194 P02766 Transthyretin 80.05% 90.71%

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.
Lupinus albus

Cross-Links

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PubChem 44260100
LOTUS LTS0270134
wikiData Q105309113