Lespeflorin I3

Details

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Internal ID ee5f54fc-83fa-4199-adb8-9b468a78e8fd
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Coumestans
IUPAC Name 8,9-dihydroxy-3-methoxy-10-(3-methylbut-2-enyl)-[1]benzofuro[3,2-c]chromen-6-one
SMILES (Canonical) CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)OC)OC3=O)C
SMILES (Isomeric) CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)OC)OC3=O)C
InChI InChI=1S/C21H18O6/c1-10(2)4-6-13-18(23)15(22)9-14-17-20(27-19(13)14)12-7-5-11(25-3)8-16(12)26-21(17)24/h4-5,7-9,22-23H,6H2,1-3H3
InChI Key OCSVLSKWXCFMKU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H18O6
Molecular Weight 366.40 g/mol
Exact Mass 366.11033829 g/mol
Topological Polar Surface Area (TPSA) 89.10 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.62
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEMBL561441

2D Structure

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2D Structure of Lespeflorin I3

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9571 95.71%
Caco-2 - 0.5321 53.21%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6993 69.93%
OATP2B1 inhibitior - 0.5670 56.70%
OATP1B1 inhibitior + 0.8725 87.25%
OATP1B3 inhibitior + 0.8754 87.54%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6695 66.95%
P-glycoprotein inhibitior + 0.6374 63.74%
P-glycoprotein substrate - 0.7092 70.92%
CYP3A4 substrate + 0.5466 54.66%
CYP2C9 substrate - 0.5890 58.90%
CYP2D6 substrate - 0.8274 82.74%
CYP3A4 inhibition - 0.7769 77.69%
CYP2C9 inhibition + 0.6793 67.93%
CYP2C19 inhibition + 0.8411 84.11%
CYP2D6 inhibition - 0.5565 55.65%
CYP1A2 inhibition + 0.5587 55.87%
CYP2C8 inhibition + 0.4541 45.41%
CYP inhibitory promiscuity + 0.7797 77.97%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4850 48.50%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.5864 58.64%
Skin irritation - 0.7483 74.83%
Skin corrosion - 0.9457 94.57%
Ames mutagenesis - 0.5364 53.64%
Human Ether-a-go-go-Related Gene inhibition - 0.6552 65.52%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8077 80.77%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8165 81.65%
Acute Oral Toxicity (c) III 0.4752 47.52%
Estrogen receptor binding + 0.9256 92.56%
Androgen receptor binding + 0.9097 90.97%
Thyroid receptor binding + 0.5927 59.27%
Glucocorticoid receptor binding + 0.8834 88.34%
Aromatase binding + 0.6846 68.46%
PPAR gamma + 0.8800 88.00%
Honey bee toxicity - 0.8474 84.74%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9941 99.41%

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 99.85% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.58% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.23% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.13% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.90% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.51% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.28% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 91.74% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.98% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.88% 99.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.94% 85.30%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.74% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.41% 89.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 86.22% 83.57%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.36% 95.50%
CHEMBL3194 P02766 Transthyretin 82.95% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.66% 95.89%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.65% 89.34%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.14% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 82.00% 93.31%
CHEMBL4208 P20618 Proteasome component C5 81.74% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.02% 99.23%
CHEMBL240 Q12809 HERG 80.64% 89.76%

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 25243076
NPASS NPC261471
ChEMBL CHEMBL561441
LOTUS LTS0129951
wikiData Q105189559