Lespecyrtin F2

Details

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Internal ID 0fbe5d61-feb4-4568-b953-cf2333d0e99d
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Furanoisoflavonoids > Pterocarpans
IUPAC Name 2,10-bis(3-methylbut-2-enyl)-6H-[1]benzofuro[3,2-c]chromene-3,8,9-triol
SMILES (Canonical) CC(=CCC1=CC2=C(C=C1O)OCC3=C2OC4=C(C(=C(C=C34)O)O)CC=C(C)C)C
SMILES (Isomeric) CC(=CCC1=CC2=C(C=C1O)OCC3=C2OC4=C(C(=C(C=C34)O)O)CC=C(C)C)C
InChI InChI=1S/C25H26O5/c1-13(2)5-7-15-9-18-22(11-20(15)26)29-12-19-17-10-21(27)23(28)16(8-6-14(3)4)24(17)30-25(18)19/h5-6,9-11,26-28H,7-8,12H2,1-4H3
InChI Key LGLLDPCJEPLYCU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H26O5
Molecular Weight 406.50 g/mol
Exact Mass 406.17802393 g/mol
Topological Polar Surface Area (TPSA) 83.10 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.13
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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CHEMBL551908

2D Structure

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2D Structure of Lespecyrtin F2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9633 96.33%
Caco-2 - 0.5655 56.55%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7535 75.35%
OATP2B1 inhibitior - 0.5667 56.67%
OATP1B1 inhibitior + 0.8924 89.24%
OATP1B3 inhibitior + 0.9707 97.07%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9255 92.55%
P-glycoprotein inhibitior + 0.7900 79.00%
P-glycoprotein substrate - 0.5539 55.39%
CYP3A4 substrate + 0.5297 52.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3752 37.52%
CYP3A4 inhibition - 0.8109 81.09%
CYP2C9 inhibition + 0.7911 79.11%
CYP2C19 inhibition + 0.7902 79.02%
CYP2D6 inhibition - 0.6617 66.17%
CYP1A2 inhibition + 0.8105 81.05%
CYP2C8 inhibition - 0.6127 61.27%
CYP inhibitory promiscuity + 0.7780 77.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6457 64.57%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.5790 57.90%
Skin irritation - 0.7503 75.03%
Skin corrosion - 0.9297 92.97%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7180 71.80%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.6448 64.48%
skin sensitisation - 0.7515 75.15%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7605 76.05%
Acute Oral Toxicity (c) III 0.5941 59.41%
Estrogen receptor binding + 0.9486 94.86%
Androgen receptor binding + 0.7883 78.83%
Thyroid receptor binding + 0.7312 73.12%
Glucocorticoid receptor binding + 0.8474 84.74%
Aromatase binding + 0.7599 75.99%
PPAR gamma + 0.9116 91.16%
Honey bee toxicity - 0.8793 87.93%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9905 99.05%

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 99.88% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 93.50% 91.49%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.40% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.43% 89.00%
CHEMBL2581 P07339 Cathepsin D 90.66% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.72% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.15% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.12% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.95% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.00% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.98% 95.89%
CHEMBL3038469 P24941 CDK2/Cyclin A 85.98% 91.38%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.95% 92.68%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 83.27% 95.58%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.70% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.91% 99.17%

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 cyrtobotrya
Teucrium betonicum

Cross-Links

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PubChem 25208758
NPASS NPC37183
ChEMBL CHEMBL551908
LOTUS LTS0068363
wikiData Q105151449