Lespeflorin H1

Details

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Internal ID bd6d5bc4-7db5-4362-b7c6-3e48d3037b62
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Furanoisoflavonoids > Pterocarpans
IUPAC Name 3-methoxy-10-(3-methylbut-2-enyl)-6H-[1]benzofuro[3,2-c]chromene-8,9-diol
SMILES (Canonical) CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)OC)OC3)C
SMILES (Isomeric) CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)OC)OC3)C
InChI InChI=1S/C21H20O5/c1-11(2)4-6-14-19(23)17(22)9-15-16-10-25-18-8-12(24-3)5-7-13(18)20(16)26-21(14)15/h4-5,7-9,22-23H,6,10H2,1-3H3
InChI Key CVWBRDWJOWRQRY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H20O5
Molecular Weight 352.40 g/mol
Exact Mass 352.13107373 g/mol
Topological Polar Surface Area (TPSA) 72.10 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.92
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEMBL565008

2D Structure

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2D Structure of Lespeflorin H1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9537 95.37%
Caco-2 + 0.6823 68.23%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7229 72.29%
OATP2B1 inhibitior - 0.7148 71.48%
OATP1B1 inhibitior + 0.8973 89.73%
OATP1B3 inhibitior + 0.9584 95.84%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8110 81.10%
P-glycoprotein inhibitior + 0.7129 71.29%
P-glycoprotein substrate + 0.5119 51.19%
CYP3A4 substrate + 0.5966 59.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3752 37.52%
CYP3A4 inhibition - 0.6985 69.85%
CYP2C9 inhibition + 0.7109 71.09%
CYP2C19 inhibition + 0.8346 83.46%
CYP2D6 inhibition - 0.5417 54.17%
CYP1A2 inhibition + 0.7868 78.68%
CYP2C8 inhibition + 0.4930 49.30%
CYP inhibitory promiscuity + 0.8188 81.88%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6597 65.97%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.6702 67.02%
Skin irritation - 0.7822 78.22%
Skin corrosion - 0.9402 94.02%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4012 40.12%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7891 78.91%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7633 76.33%
Acute Oral Toxicity (c) III 0.6291 62.91%
Estrogen receptor binding + 0.9229 92.29%
Androgen receptor binding + 0.8766 87.66%
Thyroid receptor binding + 0.7388 73.88%
Glucocorticoid receptor binding + 0.8842 88.42%
Aromatase binding + 0.7034 70.34%
PPAR gamma + 0.9140 91.40%
Honey bee toxicity - 0.8151 81.51%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9828 98.28%

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 99.91% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.86% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.57% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.72% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.54% 92.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.68% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.47% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.25% 96.95%
CHEMBL2581 P07339 Cathepsin D 89.81% 98.95%
CHEMBL3438 Q05513 Protein kinase C zeta 88.08% 88.48%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.98% 99.17%
CHEMBL240 Q12809 HERG 87.24% 89.76%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.22% 85.30%
CHEMBL4208 P20618 Proteasome component C5 87.21% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.15% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.04% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 85.91% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.78% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.33% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.83% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.82% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.99% 86.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.67% 90.24%
CHEMBL221 P23219 Cyclooxygenase-1 81.64% 90.17%

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.
Lespedeza floribunda

Cross-Links

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PubChem 25242999
NPASS NPC277480
ChEMBL CHEMBL565008
LOTUS LTS0090533
wikiData Q104971040