Flemingsin

Details

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Internal ID 46f2c0f9-3ef9-43f9-8408-19f1527f3688
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 6-prenylated isoflavanones
IUPAC Name 5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC(=C(C=C3)O)OC)CC=C(C)C)O)C
SMILES (Isomeric) CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC(=C(C=C3)O)OC)CC=C(C)C)O)C
InChI InChI=1S/C26H28O6/c1-14(2)6-9-17-23(28)18(10-7-15(3)4)26-22(24(17)29)25(30)19(13-32-26)16-8-11-20(27)21(12-16)31-5/h6-8,11-13,27-29H,9-10H2,1-5H3
InChI Key HTHLDJJBNQWUJJ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C26H28O6
Molecular Weight 436.50 g/mol
Exact Mass 436.18858861 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.60
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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Fleminphilippinin B
CHEMBL2442946
BDBM50442402

2D Structure

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2D Structure of Flemingsin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9864 98.64%
Caco-2 + 0.4896 48.96%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6166 61.66%
OATP2B1 inhibitior - 0.5638 56.38%
OATP1B1 inhibitior + 0.9186 91.86%
OATP1B3 inhibitior + 0.8785 87.85%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8655 86.55%
P-glycoprotein inhibitior + 0.7566 75.66%
P-glycoprotein substrate - 0.8271 82.71%
CYP3A4 substrate + 0.5720 57.20%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.7589 75.89%
CYP2C9 inhibition + 0.8222 82.22%
CYP2C19 inhibition + 0.9121 91.21%
CYP2D6 inhibition - 0.5283 52.83%
CYP1A2 inhibition + 0.7403 74.03%
CYP2C8 inhibition + 0.7148 71.48%
CYP inhibitory promiscuity + 0.9055 90.55%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7349 73.49%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.5671 56.71%
Skin irritation - 0.7754 77.54%
Skin corrosion - 0.9474 94.74%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3948 39.48%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5427 54.27%
skin sensitisation - 0.8246 82.46%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6632 66.32%
Acute Oral Toxicity (c) III 0.6152 61.52%
Estrogen receptor binding + 0.9551 95.51%
Androgen receptor binding + 0.7717 77.17%
Thyroid receptor binding + 0.6754 67.54%
Glucocorticoid receptor binding + 0.8476 84.76%
Aromatase binding + 0.7229 72.29%
PPAR gamma + 0.8520 85.20%
Honey bee toxicity - 0.7853 78.53%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9924 99.24%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 17400 nM
IC50
PMID: 17958396

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.08% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.98% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.03% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.49% 94.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 94.01% 98.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 91.59% 95.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.49% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.78% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 88.19% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.87% 86.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.39% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.29% 99.17%
CHEMBL3922 P50579 Methionine aminopeptidase 2 86.77% 97.28%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.64% 96.00%
CHEMBL3194 P02766 Transthyretin 85.58% 90.71%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.32% 89.34%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.42% 95.89%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 81.79% 98.21%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.46% 95.50%

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.
Erythrina sigmoidea
Flemingia macrophylla
Flemingia prostrata

Cross-Links

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PubChem 15719494
NPASS NPC256406
ChEMBL CHEMBL2442946
LOTUS LTS0006584
wikiData Q105033438